rexresearch.com


Stuff & Stuff

( September 2014 [ +/- ~ 3000 Years ] )

Sci-Tech News & Olds











Fuel-Saver Patents

Ebola for Profit

Alzheimer's Reversed

US2004119375 : Cosmic flux driven electrostatic turbine

Vitamin C vs Ebola

Fukushima Update Videos

Amy HEATON, et al : Sero-Vital-HGH ( 682% Mean increase in HGH levels )

Radionuclide Removal by Zeolite

Alexander SOLZHENETSYN : Live Not By Lies

40 Hz Lucid Dreaming

H. DAI & M. GONG : 1.5 V Electrolysis with Ni-Fe

Ruxolitinib vs Baldness

Clif HIGH : Linquistics Update

Deshawn HENRY : Solar Water Purifier

Photo Gallery



Fuel-Saver Patents

http://worldwide.espacenet.com/advancedSearch?locale=en_EP

UA37572
METHOD FOR INCREASE OF EFFECTIVENESS OF FUEL UNITS ON HYDROCARBON FUEL AND DEVICE FOR ITS IMPLEMENTATION
Method for increase of power effectiveness of fuel units at hydrocarbon fuel is in simultaneous activation of components of reaction of burning before combustion. Activation undergo both components of reaction - gaseous fuel and air by means of affecting those with high-voltage pulsing irregular electric field with strength 20-25 kV and pulse frequency 100-120 Hz.

KR20120121023
Bio activation energy pad
PURPOSE: A bio activation energy pad is provided to reduce the generation of Carbon Monoxide, Hydrocarbon, and Nitrogen Oxide due to imperfect combustion as a burning rate increases. CONSTITUTION: A bio activation energy pad comprises a bent cover plate(1), an energy pad, a lower plate cover, a completely assembled energy pad, and welding spots. The H2O contained in the air flowing into an internal combustion engine is separated into hydrogen and oxygen. The energy source from normal fuel is combined with the energy source from the hydrogen and oxygen so that the power more than 35~40% of the general power obtained from the normal fuel is provided. The amount of carbon monoxide due to the imperfect combustion is reduced as the fuel efficiency of the internal combustion engine is improved.

JPH07332176
COMBUSTING METHOD FOR LIQUID HYDROCARBON BY ELECTROMAGNETIC WAVE OF CARBONACEOUS MINERAL
PURPOSE:To reduce the exhaust gas and black smokes exhausted at combustion resulting from improvement of the combusting efficiency of an internal combustion engine which uses a liquefied hydrocarbonic fuel. CONSTITUTION:A liquefied hydrocarbonic fuel is put in fluidic contact with minerals including at least carbonic component, and thereby the hydrocarbonic fuel is irradiated with carbonic mineral electromagnetic waves within the wavelength region to generate reactions so that the molecular activation motion is induced. Thus the oxidation effect at combustion is promoted and the combusting efficiency is enhanced, and thereby the exhaust gas and black smokes are reduced.

JPS63385
WATER FUEL
PURPOSE:To obtain a water fuel which does not generate CO, CO2, etc. and has excellent fuel efficiency, by dispersing activation energy comprising a liquid hydrocarbon which has been converted into a photoelectron emitting substance by allowing it to absorb electrons in a specified amount of water consisting of polar molecules. CONSTITUTION: A contact cell is produced from a bimetal formed by the surface contact of a noble metal with a base metal to generate an electrode wave, thus emitting electrons. A liquid hydrocarbon (e.g., kerosine or gasoline) is allowed to absorb the electrons to be converted into a photoelectron emitting substance for activation energy. This activation energy is dispersed with a dispersing agent in at least 20% water consisting of polar molecules to give an objective water fuel. With this water fuel, it is the hydrogen generated by the decomposition of water that burns; therefore, the combustion gas is clean and the amount of oxygen required for combustion is about 1/10 of that required with the conventional fuel.

WO2009031989
METHOD FOR INTENSIFICATION OF GASEOUS FUEL BURNING
Method for intensification of burning gaseous fuel relates to power engineering, transportation of natural gas, metallurgical industry, branches of industry with utilization of organic industrial and domestic wastes, and can be used in installations operating on hydrocarbon gaseous fuel. The method includes formation on electrodes of electric discharge that forms electric high-voltage field that affects process of burning. At that gaseous fuel of fuel-air mix in process of injection undergo effect of electric varying high-voltage field of silent discharge with following catalytic treatment. At that treatment of gaseous fuel or fuel-air mix takes place with previous adding oxygen-containing additives, this leads to increase of content of oxygen-containing radicals at burning. One uses as well silent discharge with variable power and voltage for generation of radicals of hydrocarbons formed under effect of electric high-voltage field is kept at value from 2 to 20 kV. Besides that for generation of radicals of hydrocarbons one uses gas discharge with increased frequency and variable power. As result decrease of energy of activation of endothermic process of decomposition of hydrocarbons of gaseous fuel is provided due to previous formation of hydrocarbon radicals, hydrogen atoms, oxygen-including radicals, ions and ion-radicals in flow of gaseous fuel just before stage of burning fuel-air mix and during pre-flame treatment of gaseous fuel-air mix to burning.

JP2001064662
FUNCTIONAL WATER FOR IMPROVEMENT OF HYDROCARBON BASED LIQUID FUEL
PROBLEM TO BE SOLVED: To obtain functional water for improvement of hydrocarbon based liquid fuel capable of improving combustion efficiency of an internal-combustion engine using the hydrocarbon based liquid fuel, cleaning exhaust gas components and improving fuel consumption by adding it to the hydrocarbon based liquid fuel. SOLUTION: The functional water for improvement of hydrocarbon based liquid fuel is obtained by activation of a raw water to have minimized clusters, and in the case of adding it to the hydrocarbon based liquid fuel, the functional water is capable of minimizing the fuel in molecular level by filtering the fuel and adhering on the fuel molecules. The activation preferably comprises ceramic treatment and electrolysis treatment. A preferable hydrocarbon based liquid fuel is gasoline or light oil.

RU2011111840
DEVICE FOR MAGNETIC TREATMENT OF HYDROCARBON FUEL BASED ON CONSTANT MAGNETS
FIELD: engines and pumps.SUBSTANCE: device is equipped with magnetic field concentrators and spiral-shaped ferromagnetic magnetic conductors, constant magnets and magnetic field concentrators are combined into a magnetic system with working gaps by means of spiral-shaped ferromagnetic magnetic conductors twisted along the symmetry axis of fuel line through the angle equal to the vector offset angle of magnetic induction in every subsequent working gap relative to the preceding working gap; magnetic field concentrators are made in the form of straps from ferromagnetic material, which are fixed on a pole of constant magnet in the first section, or on free ends of ferromagnetic magnetic conductors. The housing, which encloses a magnetic system, consists of sections fixing the value of working gaps and spatial orientation of vectors of magnetic induction in each of them; connection of sections to each other is movable.EFFECT: improving fuel activation effectiveness in internal combustion engines

WO0028204
METHOD AND APPARATUS FOR IMPROVING HYDROCARBON FUEL COMBUSTION
A method for improving the combustion of hydrocarbon fuels by fuel activation comprises subjecting a flowing hydrocarbon fuel while in contact with a fuel activating material selected from Sn, Pb, their mutual alloys, and their alloys with other metals of which they make up more than 90 % by weight to a magnetic field at a temperature not exceeding 50 DEG C, and to directly feed the fuel or part of it to a combustion chamber. The thus treated fuel may be activated by a non-alternating magnetic field downstream of the alternating field. Also disclosed is a corresponding apparatus, its combination with a burner, a motor car provided with it, an activated hydrocarbon fuel and a plant for its production, and the combination of turbine means and a magnet for rotatable disposition in a hydrocarbon fuel.



US5331807
Air fuel magnetizer

Apparatus for magnetically conditioning incoming air and fuel to an internal combustion engine to improve engine operation. The air and fuel, including diesel fuel, are subject to the lines of force from opposite poles of permanent magnets mounted on the air and fuel inlet lines. In another embodiment, to reduce unwanted emissions, the exhaust leading to the catalytic converter and the catalytic converter are subject to the magnetic fields from opposite poles of permanent magnets. Another embodiments provides for the use of magnets in furnaces to improve the efficiency and reduce unwanted emissions is such devices.

BACKGROUND OF THE INVENTION

The present invention relates to magnetic air/fuel conditioning systems and more particularly to the use of magnets in the fuel and air intake lines of an internal combustion engine for reducing emissions and improving efficiency.

Currently regulated gas emissions from motor vehicles are unburned hydrocarbon (HC), carbon monoxide (CO), and oxides of nitrogen (NOx).

Unburned HC and NOx react in the atmosphere to form photo-chemical smog. Smog is highly oxidizing in the environment and is the prime cause of eye and throat irritation, bad odor, plant damage, and decreased visibility. Oxides of nitrogen are also toxic. CO impairs blood capability to carry oxygen to the brain, resulting in slower reaction times and impaired judgement.

An examination of the art reveals a number of magnetic devices which have been produced to enhance the operation of internal combustion engines by application of static magnets and electromagnetic principles.

It is known that the use of permanent magnets on the fuel line of an automotive internal combustion engine for subjecting the fuel to a magnetic field will improve the performance of the engine and reduce unwanted emissions.

It also has been shown that subjecting incoming oxygen containing gas to a a magnetic field will also increase combustion efficiency.

A number of United States Patents show the use of magnets for improving the combustion of hydrocarbon fuels in engines.

U.S. Pat. No. 3,349,354 discloses the use of magnets to impose an electro magnetic field on flowing fuel. U.S. Pat. No. 3,830,621 teaches the use of magnets to impose a north magnetic field on the flowing oxygen containing gas to reduce unwanted emissions.

U.S. Pat. No. 4,414,951 describes a system in which the fuel line is subject to a magnetic field with alternating poles. U.S. Pat. No. 4,461,262 discloses a fuel treating device in which both the incoming air and fuel are subject to longitudinal magnetic fields with alternating poles.

U.S. Pat. No. 4,568,901 shows the use of magnets on a hydrocarbon fuel carrying duct for ionizing particles of the fuel, applying the south poles of the magnets. U.S. Pat. No. 4,711,271 describes the use of magnets to subject oil to a magnetic field to reduce the buildup of undesirable materials along the inside wall of the pipe.

U.S. Pat. No. 4,755,288 discloses the use of magnets to subject fuel to a magnetic force field with poles alternating. U.S. Pat. No. 5,129,382 describes the use of magnets to impose a magnetic field on the fuel to an engine with both poles of the magnetic adjacent the fuel conduit.

U.S. Pat. No. 5,161,512 has a helical array of magnets surrounding a fuel carrying conduit to concentrate the magnetic field on the flowing fluid.

None of the preceding patents teaches the present invention.

SUMMARY OF THE INVENTION

In this invention, further improvements in fuel efficiency and emission quality are obtained by the application of magnetic fields to internal combustion engine systems to both the fuel and the air being delivered to the engine.

In accordance with the principles of this invention, magnets of a specific design are arranged so that the flowing fuel is subject to the magnetic field adjacent one pole of a magnet while the incoming air is exposed to the magnetic field adjacent the opposite pole of a magnet.

In a preferred embodiment, one or more magnets are strapped to the fuel line as close as possible to the carburetor or fuel injectors with only one pole of the magnet or magnets adjacent to or in contact with the fuel line. One or more magnets are strapped to the air intake in such a way as to magnetically expose the oxygen to the magnetic field emanating from the pole opposite that of the pole used to expose the fuel.

It is believed that the fuel and oxygen are oppositely polarized or ionized, with the result that the fuel and oxygen exhibit a stronger attraction to each other with the consequence that there is more efficient and complete bonding to each other during the combustion process.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic illustration of a preferred embodiment of this invention incorporated into an automotive internal combustion engine.

FIG. 1a is a partial cross section of a magnet shown in FIG. 2.

FIG. 2 is a section taken along 2--2 of FIG. 1.

FIG. 3 is a section similar to that of FIG. 2 except that it shows an oversized magnet.

FIG. 4 is a schematic illustration of another embodiment of this invention as applied to a catalytic converter.

FIG. 5 is a schematic illustration of still another embodiment of this invention as applied to a home or industrial heating system.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring to FIG. 1, there is illustrated an internal combustion engine 12 provided with an air inlet manifold 14, an air filter 16, a carburetion or fuel injection device 18 hereinafter referred to as a carburetor, a fuel line 22 carrying a hydrocarbon liquid fuel to carburetor 18, and engine fuel-air mixture intake manifolds 24a and 24b. The products of combustion are discharged from engine 12 through an exhaust pipe 26.

In accordance with the principles of this invention, magnetic fields are applied to the incoming air and the incoming fuel in the manner to be now described.

Mounted on air manifold 14 is a permanent bar magnet 28 attached on one side of manifold 14 with a strap 32 of suitable material such as a fabric, aluminum, or plastic.

Magnet 28 has the shape of a right angle parallelepiped with the opposite flat sides or faces containing the poles of the magnet. The face with the north pole is adjacent manifold 14 while the face with the south pole is on the side of magnet 28 opposite that of manifold 14 as indicated by the arrows. Hence, the entering air within manifold 14 is exposed to the magnetic lines of force radiating from the north pole of the magnet.

Magnet 28 provides a magnetic field of at least approximately 500 gauss, but preferably about 1500 or more gauss, to produce the effectiveness desired in this invention.

In order to protect magnet 28 from the effects of heat generated by engine 12, it will be seen from FIG. 1a that magnet 28 is provided with insulation which would include a layer of aluminum 28a to block radiant energy and a layer of thermal insulation 28b to prevent heating by conduction and radiation.

Referring also to FIG. 2, a bar magnet 34 is mounted on fuel line 22 leading into carburetor 18.

Magnet 34 is a permanent bar magnet held in place by a strap 36 of suitable non-magnetic material. Magnet 34 is similar in construction, including the insulation, to that of magnet 28 being a right angle parallepiped with the face in contact with pipe 22 being the south pole of the magnet as shown by the arrows.

The width w of magnet 34 is not in excess of the diameter or cross section of pipe 22 for reasons which will now be described in connection with FIG. 3 which shows a similarly constructed magnet 38 mounted on pipe 22. However, in FIG. 3, magnet 38 has a width which is greater than the diameter of pipe 22. It is known that in a magnet of this shape the magnetic fields adjacent the edges are more intense than the fields located adjacent intermediate areas of the faces. For example, in one magnet which was measured as to its magnetic field it was discovered that the maximum intensity of the fields adjacent the edges was 1100 gauss while at an intermediate location the field dropped off to 800 gauss. Hence, as is illustrated, a good portion of the magnetic field produced by the magnet goes to waste.

It should also be noted that the exposure of the liquid hydrocarbon fuel flowing in line 22 to the magnetic field is more critical to the effectiveness of this invention because there is a smaller amount of liquid in terms of volume compared to the gaseous supply of oxygen in air. Also, the cross section of line 22 carrying the liquid fuel is much smaller than the cross section of manifold 14 containing the air requiring a more intense application of the magnetic field. Because of the larger cross section of the air manifold, the air manifold would be provided with at least two magnets for each one on the fuel line.

Magnet 34 should have an intensity of at least 500 gauss, but preferably at least 1100 gauss and above to work effectively in accordance with the principles of this invention.

It is also critical that the air and fuel flows be subject to opposite polarities of the magnets, referred herein to as a bipolar arrangement or configuration, so that if the air is subject to the magnetic field adjacent the north pole of the magnet then the fuel must be subject to the magnetic field adjacent the south pole of the magnet, and vice versa.

The resultant conditioned fuel/air mixture magnetized in opposite polarities burns more completely, producing higher engine output, better fuel economy, more power and most importantly reduces the amount of hydrocarbons, carbon monoxide and oxides of nitrogen in the exhaust.

Another benefit of this invention is that magnetically charged fuel and air molecules with opposite polarities dissolve carbon build-up in carburetor jets, fuel injectors, and combustion chambers help to clean up the engine and maintain the clean condition.

The preferred embodiment described above is equally useful where the engine employs a carburetor or fuel injection, with the fuel magnet being mounted on the fuel line leading to the carburetor or injectors, including the use of diesel fuel.

EXAMPLE

The above invention was tested on a 1988 Chrysler Le Baron with fuel injection. 1100 gauss magnets were mounted on the air and fuel inlet lines in a bipolar configuration. It was discovered that there was a substantial reduction in the hydrocarbons found in the exhaust and that there was also a noticeable improvement in engine performance, such as faster starting and greater acceleration, and miles per gallon.

The principles of this invention are also applicable to improve the efficiency of the catalytic converter whose purpose is primarily to oxidize any remaining carbon monoxide to carbon dioxide.

Referring to FIG. 4, there is shown catalytic converter 42 connected to receive the exhaust products from engine 12 through exhaust pipe 26 and discharge through pipe 46 to a muffler (not shown).

Bar magnets 48 and 52 of design similar to those described earlier, including the insulation, are mounted on pipe 26 and converter 42, respectively, as illustrated, in a bipolar arrangement.

In the illustrated arrangement, magnet 48 is mounted with the face containing the north pole in contact with exhaust pipe 26 whereas magnet 52 has its south pole facing catalytic converter 42. If desired, the magnets may be reversed as long as the bipolar arrangement is preserved.

The arrangement of the magnets shown in FIG. 4 can be used alone or in combination with the fuel-air conditioning system illustrated in FIGS. 1-3.

Referring to FIG. 5, in another preferred embodiment, the principles of this invention are shown applied to a home or industrial heating system.

Illustrated is a furnace 70 having an air inlet 72 connected to an air manifold 74 within furncace 70, a fuel inlet line 76 with a shut off valve 78, and an exhaust manifold 82 to carry away the products of combustion.

As is understood in the art, furnace 70 may be employed to heat air or water (not shown) to be distributed for residential or industrial heating purposes. In addition, furnace 70 may burn any hydrocarbon fuel such as oil, gas, and propane.

Mounted on air mainifold 74 are a plurality of bar magnets 84 of the type previously described. Mounted on fuel inlet line 76 are similar bar magnets 86. The magnets are mounted in a bipolar arrangement, for example, with magnets 84 having their north poles facing the incoming air and magnets 86 having their south poles facing the incoming fuel. If desired, the opposite arrangement of the poles may be employed provided the bipolar arrangement is maintained. The magnets would be at least 500 gauss and preferably about 1500 gauss.

It is thus seen that there has been provided unique arrangements and method for improving the operation of internal combustion engines and furnaces, reducing unwanted emissions, and improving generally the efficiency of such systems.



You can Profit from the Ebola Plague !

Ebola Disease <info@lawyer.com> [Add to Address Book]
To: You
Subject: THE OUTBREAK OF EBOLA VIRUS IN WEST AFRICA
Date: Aug 30, 2014 3:50 PM

Hello,

My Name is Barr Marvin Wills. A client of mine who died of the EBOLA virus deposited a huge amount of money in a bank here in the
US but I don't know how much. He is a Liberian Citizen so I want you to stand in as his next of kin so that the whole fund will be yours.
And you have to keep this as a secret so that you won't get yourself into any trouble because this is going to be very easy.
We shall settle between ourselves when the whole transaction is over.

I appreciate your time and understanding.

Regards,
Barr Marvin Wills.



http://time.com/3086480/alzheimers-disease-has-been-reversed-in-mice/

Alzheimer’s Disease Has Been Reversed in Mice

Though all mice studies should be viewed with quelled excitement, a new Yale School of Medicine study shows that scientists were able to reverse Alzheimer’s disease with a single dose of a drug compound.

The researchers gave mice with Alzheimer’s a compound called TC-2153, which prohibits a protein called STEP (Striatal-Enriched tyrosine Phosphatase) from interfering with the brains’ ability to learn and make memories. Synapses in the brain need to strengthen so that the brain can turn short-term memories into long-term memories, but STEP prevents synapses from doing so, and this can lead to neurological disorders including Alzheimer’s.

The mice with memory loss who were given the compound were able to recover their cognitive function, and the researchers say they were indistinguishable from normal, control mice. The researchers, who published their recent work in the journal PLOS Biology, are now testing the compound’s ability in other animals.

It will still be a long time before a compound like this is tested in humans, but the preliminary finding is encouraging since very few experiments have actually been able to reverse the disease, which currently affects about five million Americans and is expected to grow dramatically in coming years.


http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.1001923
DOI: 10.1371/journal.pbio.1001923

Inhibitor of the Tyrosine Phosphatase STEP Reverses Cognitive Deficits in a Mouse Model of Alzheimer's Disease

Jian Xu, Manavi Chatterjee, Tyler D. Baguley, Jonathan Brouillette, Pradeep Kurup, Debolina Ghosh, Jean Kanyo, Yang Zhang, Kathleen Seyb, Chimezie Ononenyi, Ethan Foscue, George M. Anderson, Jodi Gresack,

Abstract

STEP (STriatal-Enriched protein tyrosine Phosphatase) is a neuron-specific phosphatase that regulates N-methyl-D-aspartate receptor (NMDAR) and a-amino-3-hydroxy-5-methyl-4-isoxazolepr?opionicacid receptor (AMPAR) trafficking, as well as ERK1/2, p38, Fyn, and Pyk2 activity. STEP is overactive in several neuropsychiatric and neurodegenerative disorders, including Alzheimer's disease (AD). The increase in STEP activity likely disrupts synaptic function and contributes to the cognitive deficits in AD. AD mice lacking STEP have restored levels of glutamate receptors on synaptosomal membranes and improved cognitive function, results that suggest STEP as a novel therapeutic target for AD. Here we describe the first large-scale effort to identify and characterize small-molecule STEP inhibitors. We identified the benzopentathiepin 8-(trifluoromethyl)-1,2,3,4,5-benzopenta?thiepin-6-aminehydrochloride (known as TC-2153) as an inhibitor of STEP with an IC50 of 24.6 nM. TC-2153 represents a novel class of PTP inhibitors based upon a cyclic polysulfide pharmacophore that forms a reversible covalent bond with the catalytic cysteine in STEP. In cell-based secondary assays, TC-2153 increased tyrosine phosphorylation of STEP substrates ERK1/2, Pyk2, and GluN2B, and exhibited no toxicity in cortical cultures. Validation and specificity experiments performed in wild-type (WT) and STEP knockout (KO) cortical cells and in vivo in WT and STEP KO mice suggest specificity of inhibitors towards STEP compared to highly homologous tyrosine phosphatases. Furthermore, TC-2153 improved cognitive function in several cognitive tasks in 6- and 12-mo-old triple transgenic AD (3xTg-AD) mice, with no change in beta amyloid and phospho-tau levels.

Author Summary

A series of recent studies have found that the levels of the enzyme striatal-enriched protein tyrosine phosphatase (STEP) are raised in several different neuropsychiatric and neurodegenerative disorders, including Alzheimer's disease, fragile X syndrome, and schizophrenia. STEP normally opposes the development of synaptic strengthening, and these abnormally high levels of active STEP disrupt synaptic function by removing phosphate groups from a number of proteins, including several glutamate receptors and kinases. Dephosphorylation results in internalization of the glutamate receptors and inactivation of the kinases—events that disrupt the consolidation of memories. Here we identify the benzopentathiepin 8-(trifluoromethyl)-1,2,3,4,5-benzopenta?thiepin-6-aminehydrochloride (known as TC-2153) as a novel inhibitor of STEP. We show that the mechanism of action involves the formation of a reversible covalent bond between the inhibitor and the catalytic cysteine residue of STEP, and we demonstrate the activity of TC-2153 both in vitro and in vivo. TC-2153 shows specificity towards STEP compared to several other tyrosine phosphatases and shows no toxicity to cultured neurons. Importantly, the compound reversed cognitive deficits in a mouse model of Alzheimer's disease in a way that did not involve changes in the usual pathological signs (p-tau and beta-amyloid).
Figures 123

Citation: Xu J, Chatterjee M, Baguley TD, Brouillette J, Kurup P, et al. (2014) Inhibitor of the Tyrosine Phosphatase STEP Reverses Cognitive Deficits in a Mouse Model of Alzheimer's Disease. PLoS Biol 12(8): e1001923. doi:10.1371/journal.pbio.1001923

STriatal-Enriched protein tyrosine Phosphatase (STEP) (PTPN5) is a brain-enriched protein tyrosine phosphatase (PTP) targeted in part to postsynaptic terminals of excitatory glutamatergic synapses [1]–[4]. Recent studies indicate that STEP is overactive in Alzheimer's disease (AD), schizophrenia, and fragile X syndrome (FXS) [5]–[9]. The emergent model based on these findings suggests that the increase in STEP activity interferes with synaptic strengthening and contributes to the characteristic cognitive and behavioral deficits present in these disorders.

Elevated levels of STEP activity disrupt synaptic function by dephosphorylation of STEP substrates [10]. These include mitogen-activated protein kinase (MAPK) family members ERK1/2 and p38 [11],[12], the tyrosine kinases Fyn and Pyk2 [13],[14], the glutamate receptor GluN2B subunit of NMDARs (formerly termed NR2B) [6],[15],[16], and the GluA2 subunit of AMPAR (formerly termed GluR2) [16]–[18]. STEP dephosphorylates the kinases at regulatory tyrosine residues within their activation loop and thereby inactivates them. Dephosphorylation of GluN2B promotes internalization of GluN1/GluN2B receptors, whereas dephosphorylation of GluA2 promotes internalization of GluA1/GluA2 receptors.

To test the hypothesis that the observed overexpression of STEP disrupts synaptic strengthening in AD, we crossed STEP KO mice with the 3xTg-AD and Tg2576 AD mouse models. Six-month-old progeny null for STEP displayed significant decreases in biochemical and cognitive deficits, despite continued elevated levels of Aß [16],[19]. These data validated STEP as a target for drug discovery. Herein we describe the search for small-molecule STEP inhibitors. We performed a high throughput screen that culminated in the identification of the benzopentathiepin 8-(trifluoromethyl)-1,2,3,4,5-benzopenta?thiepin-6-aminehydrochloride (known as TC-2153) as a novel STEP inhibitor. TC-2153 exhibited specificity for STEP in vitro, in cell-based assays, and in vivo, and also reversed cognitive deficits in 6- and 12-mo-old 3xTg-AD mice.

Results
Initial High Throughput Screening for STEP Inhibitors

We initially screened ~150,000 compounds from the Laboratory for Drug Discovery in Neurodegeneration library using para-nitrophenyl phosphate (pNPP) as the target substrate (see Text S1 for more information on assay development and secondary screens). Eight compounds were selected for further characterization based on chemical structure and IC50 values, which ranged between 1 µM and 9.7 µM (Table S1), and studies of these molecules indicated potent inhibition of STEP activity in neuronal cultures and cortical tissue after intraperitoneal (i.p.) injections in WT mice. However, following resynthesis of several of the lead compounds, we found that they all exhibited essentially no inhibitory activity towards STEP (Figure S1). We therefore tested the possibility that a “contaminant” in the commercial preparations of the lead compounds was inhibiting STEP activity. To address this issue, we performed preparative HPLC on Compound 3 and tested eluted fractions for activity against STEP in the pNPP assay (Figure 1A). Compound 3 appeared as a major peak (fraction 7) on the reverse-phase HPLC preparation and had no inhibitory activity against STEP compared to a second peak that appeared as a late minor peak (fraction 32) that was a potent inhibitor of STEP. Given the high apparent lipophilicity of the unknown, the supplied material was extracted with hexane and recrystallized from methanol. Small pale yellow needle-shaped crystals (0.5–1 cm in length) were obtained in approximately 1% yield. The isolated crystalline material displayed the same HPLC retention, UV absorbance, and STEP inhibitory properties as the initially collected late-eluting peak. The crystalline compound was characterized by X-ray crystallography and found to be sulfur (S8) (Figure 1B).



Magical Thinking Patented !
US2004119375
Cosmic flux driven electrostatic turbine

Inventor(s):     NEY ROBERT JOHAN [US]; BRAINARD JOHN P [US]; NEY ROBERT DOUGLAS

Abstract --- One hundred thousand years ago a Caveman observed that a thrown stone always fell to the ground, and postulated that the ground mysteriously attracted the stone. One hundred thousand years later, and 315 years after Sir Isaac Newton published his Gravitational Force Equation, most People and Physicists still believe in this myth. It is well known that charged capacitor plates exhibit significant "attractive" forces between the plates, this invention is just converting this available short linear motion to a continuous circular motion. The Energy for the resulting motion is derived completely from the Cosmic Flux Field; the Electrostatic charge of the Rotor/Stator is not depleted! The Ney-Brainard-Ney "Cosmic Flux Field Theory", and an Algorithm for calculating CF Turbine Rotor Torque is presented; they explain most of the mechanism of the "Invisible Forces at a Distance" (Gravitational, Electrostatic, and Magnetic). The Newton/Coulomb form of "Attraction" Force Equations are a great oversimplification of the Fundamental Physical Phenomena; it generally disregards the specific Attenuation/Impact Force of the Cosmic Flux traversing matter, which is the basis of all Cosmic Flux Forces! The N/C Equation "blows up" to infinity when Centroids overlap and "d<2>" in the denominator is zero. The Cosmic Flux Attenuation/Impact Forces of the Cosmic Flux paths traversing the Stators and Rotor must be Vectorially integrated, this will result in a net torque on the Rotor. In cases of relatively small Spherical mass diameters, at Astronomical distances apart, in Vacuum, of course Newton's approximation is quite accurate. The subject Cosmic Flux Electrostatic Turbine is rejected off hand by "conventional wisdom", because each element of the Stator is perfectly symmetrical to the Rotor axis "hence no net Force/Torque can exist on the Rotor". This conventional wisdom completely disregards the Fundamental Physical Phenomena.



http://jimstonefreelance.com/

Complete confirmation Vitamin C recommendation for ebola is not sabotage

Today I got final confirmation that washes with my medical knowledge, here goes:

The actual way ebola kills is by causing a severe cytokine release in blood vessel walls, which if already irritated by a viral assault, will rupture from the irritation caused by a strong cytokine release. With regard to ebola, the exact cytokine is called IL-6, which is inhibited by 41 percent with adequate vitamin C present. This means, that from this mode of action alone, vitamin C will reduce the impact of ebola by 41 percent. If you combine this with the fact that vitamin C will strengthen the blood vessel walls as well, the two ways vitamin C helps will work in combination to prevent death from ebola, especially if ebola, which removes all vitamin C weakens the blood vessel walls by removing vitamin C to begin with.



Fukushima Updates -- Videos

https://www.youtube.com/watch?v=OqeD16CqLwA
JAPAN has LITERALLY LOST Their MINDS! Fukushima update 7/25/14

https://www.youtube.com/watch?v=8H-HVDp17cg
FUKUSHIMA ITS TO LATE.JEFF RENSE

https://www.youtube.com/watch?v=PPZibmCaRSw
"HORROR " Pacific Ocean Now Dead From Fukushima Radiation

https://www.youtube.com/watch?v=NR8NqgB6ZJI
Fukushima Icke Hudes Gunderson Israel Russia NWO



Amy HEATON, et al

Sero-Vital-HGH

682% Mean increase in HGH levels

http://www.serovital.com/

So what exactly is HGH?

HGH is a single chain peptide hormone that’s manufactured deep within the brain... in the pituitary gland. It’s released into the bloodstream and travels throughout the body. It passes into your fat cells and can actually cause them to shrink. It enters your muscle cells, stimulating lean muscle growth so you look more tight and toned, even if you haven’t been working out. When it reaches the skin it maintains healthy blood flow, ramps up collagen production and strengthens the underlying substructure of the skin’s critical architecture, keeping your skin firm, tight and smooth, which is why so many experts call HGH the “youth” hormone... and why some believe it’s the key to combatting aging. The problem is that while our bodies do manufacture HGH, our levels begin to decline rapidly as we age, and until recently the best way to increase our HGH levels was through expensive prescription injections (costs can run as high as $1500 per month). In addition to their high cost, these synthetic HGH injections are also extremely controversial, because some experts fear that introducing synthetic HGH into the body may upset the natural production of HGH.

Is there a way to increase growth hormone levels by more than 600% naturally?

Until recently, the answer to that question would have been a resounding “No.” However, in September of 2012, a group of some of the most highly respected scientists in the world presented their research findings at the prestigious Obesity Society’s 30th Annual Scientific Meeting. These research results made headlines, because they showed that for the first time, there was an oral compound capable of increasing mean, bioactive, serum (blood) growth hormone levels... by 682%.

The formula that was the subject of these research findings is now being sold by SanMedica International™ under the trade name SeroVital. And despite its much-hyped research, SeroVital remained an “underground” sensation... until the famed Dr.?Oz discussed the product’s research on his show.

He introduced the show segment by asking his audience, “How many of you want to start feeling 20 years younger right now?” and then discussed what he called “a new frontier:?stimulating your body’s production of growth hormones naturally with amino acids.” And when Dr. Oz disclosed that "a recent study [on SeroVital-hgh] showed patients given a special blend of amino acids saw their HGH levels spike more than 6 times..." and added, “I have been searching for this from the day we started the show. I’ve been looking for ways of increasing HGH naturally because I don’t like getting the injections,” you can imagine the frenzy he started.

Before long, SanMedica was having trouble keeping SeroVital– with its highly specialized, patented amino acid formula – in stock. It went from underground sensation to full-blown phenomenon. Even the United States Patent Office has added to the SeroVital explosion by issuing U.S. Pat. Nos. 8,551,542, 8,715,752 and 8,722,114 protecting the SeroVital formula from imitators.

Now, after more than 30 years of time-consuming, detailed research, there’s finally an affordable oral formula that encourages the pituitary gland to increase growth hormone production naturally, with out dangerous drugs or synthetic hormone injections...


Elevated Growth Hormone 120 Minutes Following a Single Low-Dose of Amino Acids in Healthy Subjects

Background

The use of amino acid supplements to provoke growth hormone (GH) secretion in athletes and entertainers now extends to the general public. Not only do they have a goal of building lean tissue and reducing fat, but also in improving skin quality and other rejuvenating qualities that they believe GH can provide. Despite increasing mainstream use, evidence for whether oral amino acids stimulate GH is not clear.

Methods:

This was a cross-over, placebo-controlled randomized study. 16 (12 males; 32±14 years; 26.4±5.0 kg/m2) healthy subjects had serum GH measured at baseline and 15, 30, 60, 90 and 120 minutes after taking a single low dose proprietary amino acid supplement blend (SeroVital™) or placebo.

Results:

After 120 minutes, GH levels had increased 8-fold from baseline (0.17 to 1.33ng/ml) and were significantly higher than placebo (P=0.01). In addition, a significantly higher mean AUC was observed after taking the supplement [20.4 (95% CI: 19.9-21.0ng/ml) vs. 19.7 (95% CI: 18.7-20.6ng/ml); P=0.04].

Conclusions:

Our results show that a single oral dose of these amino acids can significantly increase GH Levels after 120 minutes in healthy men and women. Whether these GH changes persist over a longer duration or have other positive effects is being further examined.

Introduction

GH-deficient adults have marked reductions in lean body mass, and within months of GH treatment, gains in lean body mass, skin thickness and muscle mass were observed.1-3 It is well-established that intravenous (IV) administration of some amino acids results in significant GH secretion4,5 presumably via inhibition of somatostatin (SS), Figure 1, (also known as Growth Hormone Inhibiting Hormone). Such studies prompted testing of oral amino acids supplements (mainly arginine, lysine and orthinine) to stimulate GH secretion,6-10 albeit with mixed results and limitations in the study’s designs. Our aim was to rigorously determine whether oral amino acids can stimulate GH secretion, since athletes, entertainers and even the general public commonly take these supplements and believe GH has rejuvenating properties.

Methods

This cross-over, placebo controlled, double-blind study involved 16 healthy subjects [12 males, 4 females; 9 Caucasian, 6 African American, 1 other; mean age= 32±14 years; body mass index=26.4 ± 5.0 ranging from 19.1 to 36.8kg/m2] (IRB Number 10043). Each subject reported to the Inpatient Unit on two occasions one week apart. After an overnight fast, subjects had an IV line placed and baseline bloods samples were drawn at -30, -15, and 0 minutes. Subjects were then asked to swallow the capsules of supplement (SeroVital™) or an identical looking placebo. SeroVital™ is a novel 2.9g/dose blend of l-lysine HCl, l-arginine HCl, oxo-proline, N-acetyl-l-cysteine, l-glutamine, and schizonepeta (aerial parts) powder. Blood was drawn at 15, 30, 60and 90 and 120 minutes for assay. Human GH was measured at each time point using the Siemens Immulite 2000 (intra-assay CV was 3.72%, inter-assay CV was 5.70%, and the detection limit for GH was 0.05ng/ml.
Results

Mean growth hormone increased eight-fold over baseline (equivalent to 682%) after the supplement from 0.17 at baseline to 1.33ng/ml at 120 minutes compared to a mean decrease of 52% after placebo from 0.93 to 0.45ng/ml (Figure 2). The mean change in GH levels from baseline to 120 minutes (GH at 120 minutes minus GH at 0 minutes), was 1.15 (95% CI: 0.17, 2.14) ng/ml after the supplement versus -0.48 (-1.47, 0.50) ng/ml after the placebo, demonstrating a statistically significant differential effect (P=0.01). After the supplement, the mean AUC for GH across 120 minutes was 20.43 (95% CI: 19.90, 20.95) ng/ml/min which was significantly higher (P=0.04) than placebo at 19.67 (18.74, 20.59) ng/ml/min. Overall, 120 minutes after taking the supplement, GH levelswere significantly higher in both absolute levels and by AUC.

Discussions and Conclusions

The absolute magnitudes of these results are somewhat difficult to directly compare among past studies, as commercial GH assays use different antibodies to target specific GH epitopes resulting in differential sensitivities towards specific isoforms and fragments of the GH molecule. This results in variability of the normal range of the GH measurements in different assays. Indeed, the same GH sample measured using different assays can vary 2-3 fold.11,12 Yet mean levels of GH reached after the subcutaneous injection of 0.06 IU of HGH in the treatment of GH deficient subjects was 0.4ng/ml, a value that was clearly in the range of values seen in our study with oral amino acids.

13 Furthermore, our normalized percentage increase matches the magnitude increase of previous positive study results on GH secretion.6-10,13,14. Overall, we report an eight-fold increase, equivalent to 682%, in GH levels 120 minutes after a single oral supplement of SeroVital™.Our study had a broad range of ages and BMI’s and included both genders. An additional advantage of our study over previous GH evaluations is that it contained a placebo control group and was randomized and double-blinded. Future studies will examine whether regular increases in GH with oral amino acids increase strength and vitality. This indeed may be the case, since elderly subjects administered oral GH secretotgogues for 6 and 12 months have sustained increases in lean body mass and improved physical function.14.

1. Cuneo RC et al. J Appl Physiol 1991;70:695-700
02. Cuneo RC et al. J Appl Physiol 1991;70:688-694
03. Rudman D et al. N Engl J Med 1969;280:1434-1438
04. Merimee TJ et al. N Engl J Med 1969;280:1434-1438
05. Alba-Roth J et al. J Clin Endocrinol Metab 1988;67:1186-1189
06. Suminski RR et al. Int J Sport Nutr 1997;7:48-60
07. Lambert MI et al. Int J Sport Nutr 1993;3:298-305
08. Corpas E et al. J Gerontol 1993;48:M128-M133
09. Isidori A et al. Curr Med Res Opin 1981;7:475-481
10. Fogelholm GM et al. Int J Sport Nutr 1993;3:290-297
11. Nindl BC et al. J Appl Physiol 2001;91:163-172
12. Bidlingmaier M et al. Pituitary 2007;10:115-119
13. Janssen YJ et al. Br J Clin Pharmacol 1999;47:273-278
14. White HK et al. J Clin Endocrinol Metab 2009;94:1198-1206


US8551542
Methods and compositions for increasing growth hormones 

Inventor(s):     HEATON AMY L [US]; FRIEDLANDER MITCHELL K [US]; GAY DENNIS [US] +
 
Abstract

Embodiments of the invention generally relate to methods and supplements for improving the health of human beings.
 
FIELD OF THE DISCLOSURE

The present disclosure generally relates to methods and supplements for improving health in a subject.

BACKGROUND

The primary biological function of human growth hormone (hGH) includes stimulating growth, cell repair and regeneration. Once the primary growth period of adolescence concludes, the primary function of hGH in adulthood becomes that of cell regeneration and repair, helping regenerate skin, bones, heart, lungs, liver and kidneys to their optimal, youthful cell levels. As is the case with many of our other hormones or their pre-cursors, such as testosterone, estrogen, progesterone, DHEA and melatonin, hGH levels decline with age. Therapeutically, many of these hormones can be replaced to offset some of the effects of aging such as menopausal symptoms in women or erectile dysfunction in men.

The human body, like every other living entity, works on daily, or circadian, as well as monthly and annual rhythms. Daily growth hormone secretion diminishes with age with roughly half the levels at age forty that we had when we were twenty, and about one-third of those youthful levels at age sixty. In some sixty-year olds, the levels are as low as 25% of the hGH levels in a twenty-year old. Symptoms of aging include loss of muscle, increase of fat, decreased physical mobility, decreased energy levels and as a result, diminished socialization, diminished healing ability and an increased risk of cardiovascular disease and decreased life expectancy. Low hGH levels are associated with the aging process and early onset of disease. For example, Rosen and Bengtsson noted an increased death rate from cardiovascular disease in hGH deficient patients. (Rosen, T., Bengtsson, B. A., Lancet 336 (1990): 285-2880)

Until recently, hGH was available only in expensive injectable forms, and benefits from the restoration of hGH levels available only to those with the ability to pay. Most recently substances that can trigger the release of human growth hormone from an individual's own anterior pituitary gland have become available. These are generically referred to as secretagogues. Secretagogues have the ability to restore hGH levels, potentially to the levels found in youth. See, e.g., "Grow Young With hGH" by Dr. Ronald Klatz, President of the American Academy of Anti-Aging, published in 1997 by Harper Collins.

HGH-deficient adults have marked reductions in lean body mass, and within months of hGH treatment, gains in lean body mass, skin thickness and muscle mass are observed. (Cuneo R C et al. J Appl Physiol 1991; 70:695-700; Cuneo R C et al. J Appl Physiol 1991; 70:688-694; Rudman D et al. N Engl J Med 1969; 280:1434-1438).

It is well-established that intravenous (IV) administration of some amino acids results in significant hGH secretion. Intravenous infusion of 183 mg of arginine/kg body weight in females increased hGH levels >20-fold and 30 g of arginine elevated serum hGH levels 8.6 fold in males (Merimee T J et al. N Engl J Med 1969; 280:1434-1438; Alba-Roth J et al. J Clin Endocrinol Metab 1988; 67:1186-1189). Other amino acids, such as methionine, phenylalanine, lysine, histidine, and ornithine have also led to marked increases in hGH (Alba-Roth, Muller, Schopohl, & von Werder, 1988; Chromiak & Antonio, 2002; Gouiinelen, M., M. Donnadieu, et al. (1972) Ann Endocrinol (Paris) 33(5): 526-528).

Given the difficulties in IV administration of amino acids for widespread use, interest in elucidating the hGH response to oral amino acid supplements prompted testing of such supplements containing mainly arginine, lysine and ornithine at varying amounts. Yet the pronounced variability in results among these studies make clear the complexities involved in the design of an effective supplement for supporting hGH levels in the general public. (Suminski R R et al. Int J Sport Nutr 1997; 7:48-60; Lambert M I et al. Int J Sport Nutr 1993; 3:298-305; Corpas E et al. J Gerontol 1993; 48:M128-M133; Isidori A et al. Curr Med Res Opin 1981; 7:475-481; Fogelholm G M et al. Int J Sport Nutr 1993; 3:290-297; Chromiak J A, Antonio J. Nutrition 2002 July; 18(7-8):657-61).

BRIEF SUMMARY OF THE DISCLOSURE

Described herein are nutritional supplements and methods for using the same. In embodiments, the nutritional supplement may be an amino acid secretagogue composition, which, when administered orally, stimulates the pituitary gland of a subject to release growth hormone (e.g., hGH).

Some embodiments include an oral nutritional supplement that comprises, for example and without limitation: L-arginine hydrochloride, Oxo-proline, L-lysine hydrochloride, and cysteine. Particular examples include an oral nutritional supplement that consists essentially of L-arginine hydrochloride, Oxo-proline, L-lysine hydrochloride, N-acetyl-L-cysteine, L-glutamine, and schizonepeta powder.

Certain embodiments herein include an oral nutritional supplement dosage form that consists of 0.86 mmol L-arginine; 1.32 mmol Oxo-proline; 2.05 mmol L-lysine; 1.53 [mu]mol N-acetyl L-cysteine; 1.71 [mu]mol L-glutamine; and 125 [mu]g Schizonepta (aerial parts) powder. This oral nutritional supplement is referred to herein as "SeroVital(TM)." SeroVital(TM) may be orally administered in an amount of, for example, 2.9 grams (i.e., 4 unit dosage forms) to a human being, so as to stimulate the release of hGH in the human being. The nutritional supplement may be administered on a regular basis, such as a weekly or monthly intake at a dosage tailored to the subject's needs; i.e., the nutritional supplement may be administered regularly as multiples (1*, 2*, etc.) of the structural units (pills, tablets, capsules, etc.) in accordance with the needs of the subject.

Some embodiments include a method for increasing growth hormone (e.g., hGH) in a subject (e.g., a human subject) that comprises orally administering a nutritional supplement to a subject to improve one or more objective health metrics, including for example and without limitation: increasing lean body mass; reducing obesity, adipose tissue mass, and anxiety; supporting weight loss; decreasing appetite and atrophic processes in skeletal muscle, liver, kidney, spleen, skin, and bone; and improving at least one of energy, endurance, sleep, metabolism, heart rate, blood pressure, cardiovascular health, sympathetic nervous activity, thyroid response, glucose utilization, mental/cognitive function, reaction time, bone density, hair health and appearance, nail health and appearance, skin health and appearance, and libido.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 includes a plot of growth hormone levels measured in subjects after administration of an exemplary supplement compared to a placebo;

FIG. 2 includes a scatter plot and linear regression analysis of the time to fall asleep in subjects with continued use of an exemplary supplement over time; and

FIG. 3 includes a scatter plot and linear regression analysis of the time awake during sleep over time in subjects with continued use of an exemplary supplement.

DETAILED DESCRIPTION

The determination of an effective and safe oral functional blend that stimulates hGH secretion in the general population is important, since athletes, entertainers, and now the general public, seek effective hGH support supplements and understand hGH to have rejuvenating properties. Indeed, once partial to athletes and entertainers, the desire for effective supplements to provoke hGH increases now extends to the general public. Not only do they have a goal of building lean tissue and reducing fat, but also of improving skin quality and providing other rejuvenating qualities that hGH is understood to provide.

However, the literature on oral amino acids for use in stimulating hGH does not contain clear evidence for an optimized oral amino acid-containing blend able to stimulate hGH in the general public, including both men and women of a wide age range.

Embodiments herein provide a nutritional supplement for elevating growth hormone (e.g., hGH) release. Particular embodiments provide an amino acid-containing composition that is well tolerated, and may have the result of increasing or elevating hGH release in those individuals whose hGH release rates have slowed as a function of increasing age, or that have normal hGH levels but desire higher hGH levels. Although some existing nutritional supplements claim to impact the production of natural human growth hormone, there is a need for an improved nutritional supplement that efficiently enhances the production and effect of natural human growth hormone in the general population.

Some embodiments herein provide a nutritional supplement for use by a human being. In particular embodiments, the nutritional supplement is an amino acid secretagogue composition, which, when administered orally, may stimulate the pituitary gland to produce hGH. Increased production of hGH may result in inhibition of insulin depression; inhibition of hyperglycaemia and increase in insulin effectiveness; enhancement of fat conversion; lowering of cholesterol; and/or normalization of lipid balance. In examples, a supplement herein may function as a dietary supplement by assisting the body's own ability to secrete hGH naturally in a manner which is safe and effective. Such a supplement may provide growth hormone therapy in a more affordable manner than existing compositions and methods, for example, injectable hGH compositions.

Particular embodiments herein include an oral nutritional supplement that comprises L-lysine, L-arginine, oxo-proline, and one of cysteine and glutamine. In some examples, a supplement herein may comprise both cysteine and glutamine and/or schizonepeta powder. In particular examples, a functional dosage includes the L-arginine at a level between about 0.1-6 moles and the oxo-proline between about 0.1-8 moles, and/or the L-lysine in an amount between about 0.1-12 moles. In particular examples, the cysteine and/or glutamine may be contained at a level between about 0.001-6 moles.

Cysteine may be present in a supplement according to particular embodiments as n-acetyl L-cysteine, and the glutamine may be L-glutamine. Amino acids in a nutritional supplement herein may be delivered as non-toxic salts thereof, effective complexes thereof, stable chelates thereof, active esters thereof, functional derivatives thereof, and mixtures thereof which are effective to increase hGH levels in a subject from the general population.

Particular embodiments herein include an oral nutritional supplement that consists essentially of L-lysine (e.g., L-lysine HCl), L-arginine (e.g., L-arginine HCl), oxo-proline, N-acetyl-L-cysteine, L-glutamine, and schizonepeta (aerial parts) powder. In particular examples, a functional dosage includes L-arginine at a level between about 0.1-6 moles and oxo-proline between about 0.1-8 moles, and/or L-lysine in an amount between about 0.1-12 moles. n-acetyl L-cysteine and/or L-glutamine may be comprised in some exemplary supplements at a level between about 0.001-6 moles. In particular examples, a functional dosage includes L-arginine at a level between about 2.5-4.5 moles and oxo-proline between about 4-6 moles, and/or L-lysine in an amount between about 7-9 moles. N-acetyl L-cysteine and/or L-glutamine may be comprised in some exemplary supplements at a level between about 0.001-0.5 moles.

Certain embodiments herein include an oral nutritional supplement dosage form that consists of 0.86 mmol L-arginine; 1.32 mmol Oxo-proline; 2.05 mmol L-lysine; 1.53 mmol N-acetyl L-cysteine; 1.71 [mu]mol L-glutamine; and 125 [mu]g Schizonepta (aerial parts) powder (SeroVital(TM)). Thus, an oral nutritional supplement dosage form may consist of 181.38 mg L-arginine HCl; 170.93 mg L-pyroglutamic acid; 374.83 mg L-lysine HCl; 0.25 mg N-acetyl L-cysteine USP; 0.25 mg L-glutamine; and 0.125 mg Schizonepta (aerial parts) powder, for example, in a capsule. In some examples, the oral nutritional supplement may be administered to a human being by orally administering 4 such dosage fauns (i.e., 725.50 mg L-arginine HCl; 683.70 mg L-pyroglutamic acid; 1499.30 mg L-lysine HCl; 1.00 mg N-acetyl L-cysteine USP; 1.00 mg L-glutamine; and 0.50 mg Schizonepta (aerial parts) powder).

Some embodiments herein provide a method for increasing human growth hormone in humans that comprises orally administering a nutritional supplement for elevating growth hormone release to a healthy human being. As used herein, a "healthy human being" refers to a human being having any age-related decline in hGH, excluding any physiological deficiency that is not age-related. Particular embodiments include oral administration of a nutritional supplement for elevating growth hormone release to a human that is at least 30 years old.

A nutritional supplement for elevating growth hormone release may be orally administered to a human being to improve health, including by: increasing lean body mass; reducing obesity, adipose tissue mass, and anxiety; supporting weight loss; decreasing appetite and atrophic processes in skeletal muscle, liver, kidney, spleen, skin, and bone; and improving energy, endurance, sleep, metabolism, heart rate, blood pressure, cardiovascular health, sympathetic nervous activity, thyroid response, glucose utilization, mental/cognitive function, reaction time, bone density, hair health and appearance, nail health and appearance, skin health and appearance, and libido.

In certain examples, oral administration of a nutritional supplement for elevating growth hormone release may improve hair and/or nail thickness, length, and/or growth. Oral administration of a nutritional supplement for elevating growth hormone release may improve wound healing, provide anti-aging skin properties, reduce wrinkles, dark spots, discolorations, dullness, sagging, laxity, and thinning, and may further improve texture, luminosity, "lift," tone, radiance, smoothness, uniformity, and youthful look of skin.

A nutritional supplement for elevating growth hormone release may also be used in combination with testosterone or testosterone-boosting supplements to enhance the effect of the nutritional supplements disclosed herein.

In accordance with the "consist essentially of" and "consisting essentially of" language herein, a nutritional supplement for elevating growth hormone release in some embodiments is essentially limited to the aforementioned ingredients, and does not include any additional active ingredients intended to add nutritional content (e.g., vitamins, minerals, etc.), but may include additional ingredients not intended to add nutritional content, for example, ingredients intended to fulfill a non-nutritional purpose (e.g., coloring, fillers, flavoring, an ingredient for maintaining the structural form, etc.).

Each ingredient of a nutritional supplement for elevating growth hormone release may be prepared in accordance with any method known to one of ordinary skill in the art. Alternatively, each ingredient may be obtained in a fully-prepared from a commercially available source.

A nutritional supplement for elevating growth hormone release may be in any suitable oral administration form, including but not limited to: a chewable form, a liquid form, a spray form, a capsule form, a suppository form, dissolvable wafer, and a powder form. In some embodiments, a dosage form of the nutritional supplement may be present in an amount of about 2.9 grams.

Irrespective of the structural form of the nutritional supplement for elevating growth hormone release, the ingredients of the nutritional supplement may be distributed homogeneously or non-homogeneously within the nutritional supplement.

A nutritional supplement for elevating growth hormone release may be ingested on a regular basis, such as a daily or weekly intake at a dosage tailored to an individual's needs; i.e., the nutritional supplement is to be taken regularly as multiples (1*, 2*, etc.) of the dosage form (e.g., pills, tablets, capsules, etc.) in accordance with the needs of the individual. For example, a senior citizen leading a sedentary life is likely to need higher daily doses than does a young person engaged in regular strenuous exercise (e.g., a weight lifter). Alternatively, the nutritional supplement for elevating growth hormone release may be ingested on an as-needed basis at a dosage tailored to the individual's needs. Medical or nutritional counseling may be beneficial for arriving at a desirable or optimal dosage tailored to the individual's needs. The nutritional supplement may be administered, for example, from one to three times daily, or, by way of further example, the supplement may be administered every other day, or once a week. In particular embodiments, the nutritional supplement may be administered on an empty stomach.

In embodiments, a nutritional supplement for elevating growth hormone release comprises a particular combination of types of amino acids, mass ranges, and specific formulations that have been selected to be synergistically-balanced and of adequate quantity to achieve a desired physiological effect; i.e., growth hormone release. Improper combinations of the same amino acids may be ineffective. The component amino acids may be synergistic in the sense that several of them, when combined together, synergistically stimulate the release of human growth hormone. The combination of amino acids in particular embodiments was also chosen to reduce or inhibit chemical combination or reaction between the amino acids.

EXAMPLES

Example 1

Effect of an Oral Nutritional Supplement Single Dose on hGH Levels

The short-term effects of a single oral nutritional supplement on hGH levels 2 hours post ingestion was studied 16 healthy subjects [12 males, 4 females; 9 Caucasian, 6 African American, 1 other; mean age=32+-14 years; body mass index=26.4+-5.0 ranging from 19.1 to 36.8 kg/m<2>]. Each subject reported to the Inpatient Unit on two occasions one week apart. After an overnight fast, subjects had an IV line placed and baseline bloods samples were drawn at -30, -15, and 0 minutes.
Subjects were then asked to swallow the capsules of supplement (SeroVital(TM)) or an identical looking placebo. SeroVital(TM) is a 2.9 g/dose blend of L-lysine HCl, L-arginine HCL, oxo-proline, N-acetyl-L-cysteine, L-glutamine, and schizonepeta (aerial parts) powder. Blood was drawn at 15, 30, 60 and 90 and 120 minutes for assay. Human GH was measured at each time point using the Siemens Immulite(TM) 2000 (intra-assay CV was 3.72%, inter-assay CV was 5.70%, and the detection limit for GH was 0.05 ng/mL. The -15 and 120 minute time points were additionally assayed for triiodothyronine (T3) as informative for mechanistic investigations.

The mean growth hormone increased 682% after the supplement from 0.17 at baseline to 1.33 ng/mL at 120 minutes, compared to a mean decrease of 52% after the placebo from 0.93 to 0.45 ng/mL. FIG. 1.

The mean change in GH levels from baseline to 120 minutes (GH at 120 minutes minus GH at 0 minutes), was 1.15 (95% CI: 0.17, 2.14) ng/mL after the supplement, versus -0.48 (-1.47, 0.50) ng/mL after the placebo, demonstrating a statistically-significant differential effect (P=0.01). After the supplement, the mean AUC for GH across 120 minutes was 20.43 (95% CI: 19.90, 20.95) ng/mL/min which was significantly higher (P=0.04) than placebo at 19.67 (18.74, 20.59) ng/mL/min. Overall, 120 minutes after taking the supplement, GH levels were significantly higher in absolute levels or by AUC.

As daily circadian levels of T3 naturally decrease during the morning hours, at which the current trial was scheduled, it was not surprising that placebo levels between the -15 and 120 minute time points decreased by -6.10 ng/dL (106 to 100 ng/dL, P=0.01). In contrast, the SeroVital(TM) group exhibited a deceased reduction in T3 by nearly one-half over the same time course, -3.3 ng/dL (101-97.3 ng/dL, NS), which was not a significant reduction compared to baseline, as was the reduction in the placebo group. These results affirm that somatostatin inhibition plays a mechanistic role in the ability of SeroVital(TM) to induce significant increases in serum GH levels in human subjects.

At 120 minutes, GH concentrations were 2-fold higher in women (2.3+-1.1 ng/mL, n=4) than in men (1.0+-0.4 ng/mL, n=12, although the study was not adequately powered for these comparisons. Nevertheless, these findings support an enhanced effect of the SeroVital(TM) supplement in women.

An eight-fold increase was observed, equivalent to 682%, in GH levels 120 minutes after a single oral supplement of SeroVital(TM). The study had a broad range of ages and BMI's and included both genders. An additional advantage of the present study over previous GH evaluations is that it contained a placebo control group and was randomized and double-blinded.

These findings demonstrate that a specialized low-dose amino acid supplement can significantly increase short-term GH levels. Future studies will examine whether such increases in GH with oral amino acid supplementation increase fat-free mass and strength. This indeed may be the case, since elderly subjects administered oral GH secretagogues for 6 and 12 months have sustained increases in lean body mass and improved physical function.

The absolute magnitudes of these results are somewhat difficult to directly correlate among past studies, as commercial GH assays use different antibodies to target specific GH epitopes. Therefore, different antibodies and assays are less likely to recognize some specific isoforms and fragments of the GH molecule. This results in variability of the normal range of the GH measurements in different assays. Indeed, the same GH sample measured using different assays can vary 2-3 fold, limiting the ability to compare actual GH levels across studies. Nevertheless, the mean levels of GH reached after the subcutaneous injection of 0.06 IU of HGH in the treatment of GH deficient subjects was 0.4 ng/mL, a value that was clearly in the range of values seen in our study with oral amino acids.

Findings obtained from a randomized, blinded, placebo-controlled study strengthen the evidence that oral administration of amino acids, when compounded properly, can increase GH serum levels, wherein SeroVital(TM) administration showed an 8-fold increase, equivalent to a 682% increase in GH levels, 120 minutes after a single oral dose. In addition, we elucidate some mechanistic details for these significant GH increases as through somatostatin inhibition, supported by our results on the 120 minute results on T3 levels in the same subjects.

Example 2

Effect of an Oral Nutritional Supplement on Endurance and Fat Metabolism

To test the effect of the nutritional supplement on endurance and fat metabolism, a double-blind clinical study was conducted involving 12 healthy subjects [7 males, 5 females; mean age=31+-6 years; body mass index=25.7+-3.8 ranging from 20.3 to 32.2 kg/m<2>]. Each subject reported to the Fitness Testing Facility (PEAK, University of Utah College of Health) after an overnight fast. Upon arrival, each subjects underwent standard measurements of weight, height, body fat percent (Bod Pod), and resting metabolic rate (RMR, indirect calorimerty). Daily calorie expenditure was estimated based on the additive evaluations of measured RMR, estimated Lifestyle and Activity (defined as the number of calories burned performing daily activities including working, playing eating, etc), and estimated Exercise (defined as an estimate of the number of calories burned during exercise based on daily activity level). Following the baseline measurements, subjects then consumed a standard breakfast (Egg McMuffin, 300 Calories; 12 g fat; 29 g carbohydrates; 18 g protein). Subjects rested for a further 45 minutes to reach a post-absorptive state, then underwent a Maximal Aerobic Fitness Test of graded exercise, completed on a treadmill. Subjects' oxygen uptake was measured using a metabolic cart, and VO2max was quantified.
Subjects were then provided a two week supply of a novel supplement SeroVital(TM) (2.9 g/dose blend of L-lysine HCl, L-arginine HCl, oxo-proline, N-acetyl-L-cysteine, L-glutamine, and schizonepeta (aerial parts) powder). The novel SeroVital(TM) increases serum human growth hormone hGH levels by 8 times (equivalent to 682%) 120 minutes after a single dose in healthy male and female volunteers. In this study, subjects were instructed to consume one dose of the supplement on an empty stomach, two hours after dinner prior to bedtime, every night for the two-week study duration.

Following the final dose, each subject returned to the PEAK Fitness Testing Facility, University of Utah College of Health after an overnight fast (without having consumed their last dose of the supplement since the previous night). Upon arrival, each subjects underwent the identical test protocols as the baseline test day. The data from the two measurement days were then analyzed. Consistent with the hypothesis that the supplement would increase improve endurance parameters with its ability to increase in hGH levels, the decision was made to reject the null only if the data supported the one directional alternative consistent with a favorable response to the supplement. Statistical significance was assumed for P<=0.05.

Mean VO2max increased by 6% from 44.9+-8.1 at baseline to 47.7+-9.2 mL/kg/min (3.69+-0.96 to 3.91+-1.02 L/min), demonstrating a statistically significant differential effect compared to baseline (P=0.02). After the period of supplementation with SeroVital(TM), the mean RMR increased by 2.7% from 1687+-330 to 1733+-288 kcal/day with a statistical trend towards significance compared to baseline (P=0.165). Estimated daily calorie expenditure also increased by 2.7% from 1687+-330 to 1733+-288 kcal/day with the trend towards significance (P=0.166).

After two weeks of supplementation with the supplement SeroVital(TM), (taken on an empty stomach, two hours after dinner prior to bedtime, every night), both RMR and estimated daily calorie expenditure tended to increase, evidencing the potential of the supplement to impart long-term fat burning effects. Additionally, endurance as measured by VO2max in the post-absorptive state significantly improved with a measured 6% increase. Overall, the SeroVital(TM) supplement was shown to increase parameters of endurance, energy, and vitality.

Example 3

Effect of an Oral Nutritional Supplement on Sleep Improvement

To test the ability of the nutritional supplement to improve sleep, a double-blind clinical study was conducted involving 15 healthy subjects [10 males, 5 females; mean age=33+-7 years]. Each subject completed a baseline Epworth Sleepiness Scale self-report questionnaire and a standardized assay of usual sleep habits. All subjects were deemed to have average sleep parameters within a normal range.

The subjects were then provided a three week supply of a novel supplement SeroVital(TM) (2.9 g/dose blend of L-lysine HCl, L-arginine HCl, oxo-proline, N-acetyl-L-cysteine, L-glutamine, and schizonepeta (aerial parts) powder). The novel SeroVital(TM) blend increases serum human growth hormone hGH levels by 8 times (equivalent to 682%) 120 minutes after a single dose in healthy male and female volunteers.

We investigated sleep patterns with continued use of the supplement when taken on an empty stomach, two hours after dinner prior to bedtime, every night for three weeks. On each trial day, subjects reported 1) time went to bed; 2) time of final wakening; 3) estimated time to fall asleep; 4) time of awakening during sleep/length of time awake. Data was compiled by day for estimated time to fall asleep and length of time awake during sleep in order to assess sleep efficiency. Daily values for each measure were plotted as an average (+-S.D.) among the subjects over the time course of the study, and a linear regression was tabulated to assess overall trends over time. All available data was included in the analysis.

Linear regression analysis showed that both estimated time to fall asleep (FIG. 2) and time awake during sleep (FIG. 3) tended to decrease over time with continued use of the supplement over the time course of the study. The time to fall asleep decreased with an average slope of -0.24 min/day, and the time awake during sleep decreased by an average slope of -0.26 min/day. Overall, these results so a trend towards greater sleep efficiency by measurements of both time to fall asleep and time awake during sleep, both with a quantified average decrease of about 0.25 min/day over three weeks with regular nighttime use of the novel SeroVital(TM) supplement (when taken as directed, on an empty stomach, two hours after dinner prior to bedtime).

Example 4

Effect of an Oral Nutritional Supplement on Lean Body Mass and Weight Change

To test the effect of the nutritional supplement on lean body mass and weight change of humans, healthy men and women between the ages of 30 to 80 years are recruited through advertisements. Standardized assessment criteria are used to select subjects at risk for functional decline (e.g., hand grip strength, habitual gait speed, etc.). Additionally, subjects are excluded for diabetes mellitus, use of anticoagulants, seizure disorder, cancer treatment within five years, poorly controlled hypertension, unstable or recent onset angina, myocardial infarction within 6 months, cognitive impairment, depression, significant limitations of lower extremity function, bradycardia, systolic blood pressure <100 or >170 mm Hg, or orthostatic hypotension. Subjects participating in strength training programs were also excluded.
Subjects are given daily doses of the nutritional supplement for 6 months at different dosing concentrations of active ingredients, and one group is treated as a placebo group. The study includes a pre-screening assessment, screening and baseline visits, and weekly visits over the planned 6 months, where weight, body composition, and physical performance (including endurance) are determined, along with hormonal data analysis. Weight, percent lean body mass, and percent fat body mass are chosen as primary measures of body composition at the 6 month analysis period.

Example 5

Effect of an Oral Nutritional Supplement on Energy, Bone Density, Skin Thickness, and Mass of Adipose Tissue

To test the effect of the nutritional supplement on energy, bone density, skin thickness, and mass of adipose tissue of healthy men over 60 years old are recruited through advertisements. Standardized assessment criteria are used to select subjects at risk for functional decline (e.g., hand grip strength, habitual gait speed, etc.). Entry criteria includes body weight of 90 to 120 percent of the standard for age. Additionally, subjects are excluded for diabetes mellitus, use of anticoagulants, seizure disorder, cancer treatment within five years, poorly controlled hypertension, unstable or recent onset angina, myocardial infarction within 6 months, cognitive impairment, depression, significant limitations of lower extremity function, bradycardia, systolic blood pressure <100 or >170 mm Hg, or orthostatic hypotension. Subjects participating in strength training programs were also excluded.

Subjects are given daily doses of the nutritional supplement for 6 months at different dosing concentrations of active ingredients, and one group is treated as a placebo group. The study includes a pre-screening assessment, screening and baseline visits, and weekly visits over the planned 6 months, where lean body mass, mass of adipose tissue, skin thickness, and bone density at various skeletal sites are measured. Subjects are also monitored for changes in energy levels throughout the experiment.

Example 6

Effect of an Oral Nutritional Supplement on Anxiety and Sleep

To test the effect of the nutritional supplement on anxiety and sleep, healthy men and women between the ages of 30 to 80 years are recruited through advertisements. Subjects are interviewed by a psychiatrist using the Structured Clinical Interview for DSM-III-R or analogous method. Patients are all drug free. The study focuses on the evaluation of anxiety, sleep patterns, and measurement of basal morning stress hormone levels at various points during the 6 month testing period.
Subjects are given daily doses of the nutritional supplement for 6 months at different dosing concentrations of active ingredients, and one group are treated as a placebo group. The study includes a pre-screening assessment, screening and baseline visits, and weekly visits over the planned 6 months, where anxiety assessment (e.g., Hamilton Anxiety Rating Scale), and anxiety and stress hormone levels (e.g., cortisol and GH) are determined, and sleep study analysis are conducted.

   
COMPOSITIONS FOR INCREASING HUMAN GROWTH HORMONE LEVELS 
US8715752

Abstract

Embodiments of the invention generally relate to supplements for increasing human growth hormone (hGH) levels in healthy human beings.

TECHNICAL FIELD

[0001] Embodiments of the invention generally relate to supplements for increasing human growth hormone (hGH) levels in healthy human beings.

BACKGROUND

[0002] The primary biological function of hGH includes stimulating growth, cell repair and regeneration. Once the primary growth period of adolescence concludes, the primary function of hGH in adulthood becomes that of cell regeneration and repair, helping regenerate skin, bones, heart, lungs, liver and kidneys to their optimal, youthful cell levels. As is the case with many of our other hormones or their pre-cursors, such as testosterone, oestrogen, progesterone, DHEA and melatonin, hGH levels decline with age. Therapeutically, many of these hormones can be replaced to offset some of the effects of aging such as menopausal symptoms in women or erectile dysfunction in men. The human body, like every other living entity, works on daily, or circadian, as well as monthly and annual rhythms Daily growth hormone secretion diminishes with age with roughly half the levels at age forty that we had when we were twenty, and about one-third of those youthful levels at age sixty. In some sixty-year olds, the levels are as low as 25% of the hGH levels in a twenty-year old. Symptoms of aging include loss of muscle, increase of fat, decreased physical mobility, decreased energy levels and as a result, diminished socialization, diminished healing ability and an increased risk of cardiovascular disease and decreased life expectancy. Low hGH levels are associated with the aging process and early onset of disease. For example, Rosen and Bengtsson noted an increased death rate from cardiovascular disease in hGH deficient patients (Rosen, T., Bengtsson, B. A., Lancet 336 (1990): 285-2880).

[0003] Until recently human growth hormone (hereinafter alternatively referred to as hGH) was available only in expensive injectable forms, and benefits from the restoration of hGH levels available only to those with the ability to pay. Most recently substances that can trigger the release of human growth hormone from an individual's own anterior pituitary gland have become available. These are generically referred to as secretagogues. Secretagogues have the ability to restore hGH levels, potentially to the levels found in youth. See for reference the book entitled "Grow Young With hGH" by Dr. Ronald Klatz, President of the American Academy of Anti-Aging, published in 1997 by Harper Collins.

[0004] HGH-deficient adults have marked reductions in lean body mass, and within months of hGH treatment, gains in lean body mass, skin thickness and muscle mass are observed. (Cuneo R C et al. J Appl Physiol 1991;70:695-700; Cuneo R C et al. J Appl Physiol 1991;70:688-694; Rudman D et al. N Engl J Med 1969;280:1434-1438).

[0005] It is well-established that intravenous (IV) administration of some amino acids results in significant hGH secretion. Intravenous infusion of 183 mg of arginine/kg body weight in females increased hGH levels>20-fold and 30 g of arginine elevated serum hGH levels 8.6 fold in males (Merimee T J et al. N Engl J Med 1969;280:1434-1438; Alba-Roth J et al. J Clin Endocrinol Metab 1988;67:1186-1189). Other amino acids, such as methionine, phenylalanine, lysine, histidine, and ornithine have also led to marked increases in hGH (Alba-Roth, Muller, Schopohl, & von Werder, 1988; Chromiak & Antonio, 2002; Gourmelen, M., M. Donnadieu, et al. (1972) Ann Endocrinol (Paris) 33(5): 526-528).

[0006] Given the difficulties in IV administration of amino acids for widespread use, interest in elucidating the hGH response to oral amino acid supplements prompted testing of such supplements containing mainly arginine, lysine and ornithine at varying amounts. Yet the pronounced variability in results among these studies, which differed in aspects including subject population, supplement composition, and dosage methodologies, make clear the complexities involved in the design of an effective supplement for supporting hGH levels in the general public. (Suminski R R et al. Int J Sport Nutr 1997;7:48-60; Lambert M I et al. Int J Sport Nutr 1993;3:298-305; Corpas E et al. J Gerontol 1993;48:M128-M133; Isidori A et al. Curr Med Res Opin 1981;7:475-481; Fogelholm G M et al. Int J Sport Nutr 1993;3:290-297; Chromiak J A, Antonio J. Nutrition 2002 July;18(7-8):657-61).

[0007] Thus determination of an effective and safe oral functional blend that stimulates hGH secretion in the general population is important to determine since athletes, entertainers and now the general public seek effective hGH support supplements and understand hGH to have rejuvenating properties.

[0008] Indeed, once partial to athletes and entertainers, the desire for effective supplements to provoke growth hormone (hGH) increases now extends to the general public. Not only do they have a goal of building lean tissue and reducing fat, but also in improving skin quality and other rejuvenating qualities that hGH is understood to provide. Despite proceeding literature on oral amino acids for use in stimulating hGH, evidence for an optimized oral amino acid-containing blend able to stimulate hGH in the general public including both men and women of a wide age range is not clear.

[0009] It would be desirable to provide a nutritional supplement for elevating hGH release, in particular an amino acid-containing composition that is well tolerated having the result of increasing or elevating hGH release in those individuals whose hGH release rates have slowed as a function of increasing age or that have normal hGH levels but desire higher hGH levels. Although some existing nutritional supplements claim to impact the production of natural human growth hormone, there is a need for an improved nutritional supplement that efficiently enhances the production and effect of natural human growth hormone in the general population.

BRIEF SUMMARY OF THE INVENTION

[0010] The present invention is a nutritional supplement. It is a novel amino acid-containing secretagogue composition, which, taken orally, stimulates the pituitary gland to increase serum levels of hGH.

[0011] A particular embodiment of the present disclosure relates to an oral nutritional supplement that includes the amino acids 1-lysine, 1-arginine, oxo-proline, and one of either cysteine or glutamine. The amino acids may be delivered as non-toxic salts thereof, effective complexes thereof, stable chelates thereof, active esters thereof, functional derivatives thereof, and mixtures thereof which are effective to increase hGH levels in the general population.

[0012] Another particular embodiment relates to an oral nutritional supplement that consists essentially of 1-lysine HCl, 1-arginine HCl, oxo-proline, N-acetyl-1-cysteine, 1-glutamine, and schizonepeta (aerial parts) powder.

BRIEF DESCRIPTION OF THE FIGURES

[0013] FIG. 1 shows growth hormone levels after supplement administration compared to a placebo.

DETAILED DESCRIPTION OF THE INVENTION

[0014] The present invention relates to a nutritional supplement for use by a human being. The nutritional supplement is an amino acid-containing secretagogue composition, which, taken orally, stimulates the pituitary gland to increase serum levels of hGH. Increased levels of hGH may result in inhibition of insulin depression, inhibition of hyperglycaemia and increase in insulin effectiveness, enhancement of fat conversion, lowering of cholesterol, and normalization of lipid balance. The supplement of the present invention works as a dietary supplement by assisting the body's own ability to secrete hGH naturally in a manner that is safe and effective, as well as being affordable.

[0015] A particular embodiment of the present disclosure relates to an oral nutritional supplement that includes 1-lysine, 1-arginine, oxo-proline, and one of either cysteine or glutamine. The supplement may additionally include both cysteine and glutamine and/or schizonepeta powder. In particular embodiments, a functional dosage includes the 1-arginine at a level between 0.1-6 mmol and the oxo-proline between 0.1-8 mmol, and/or the 1-lysine in an amount between 0.1-12 mmol. The cysteine and/or glutamine may be contained at a level between 0.001-6 mmol. In another particular embodiment, a functional dosage includes the 1-arginine HCl at a level between 2.5-4.5 mmol and the oxo-proline between 4-6 mmol, and/or the 1-lysine HCl in an amount between 7-9 mmol The cysteine and/or glutamine may be contained at a level between 0.001-0.5 mmol. The cysteine can be n-acetyl L-cysteine and the glutamine may be 1-glutamine. The amino acids may be delivered as non-toxic salts thereof, effective complexes thereof, stable chelates thereof, active esters thereof, functional derivatives thereof, and mixtures thereof which are effective, to increase hGH levels in the general population. The nutritional supplement may be present in an amount of 2.9 grams. The nutritional supplement may be in any acceptable and known oral formulation, such as powder, tablet, capsule, liquid, or wafer form.

[0016] Another particular embodiment relates to an oral nutritional supplement that consists essentially of 1-lysine HCl, 1-arginine HCl, oxo-proline, N-acetyl-1-cysteine, 1-glutamine, and schizonepeta (aerial parts) powder. In particular embodiments, a functional dosage includes the 1-arginine HCl at a level between 0.1-6 mmol and the oxo-proline between 0.1-8 mmol, and/or the 1-lysine HCl in an amount between 0.1-12 mmol. The n-acetyl L-cysteine and/or 1-glutamine may be contained at a level between 0.001-6 mmol. In another particular embodiment, a functional dosage includes the 1-arginine HCl at a level between 2.5-4.5 mmol and the oxo-proline between 4-6 mmol, and/or the 1-lysine HCl in an amount between 7-9 mmol. The n-acetyl L-cysteine and/or 1-glutamine may be contained at a level between 0.001-0.5 mmol. The nutritional supplement may be in any acceptable and known oral formulation, such as powder, tablet, capsule, liquid, or wafer form.

[0017] Other embodiments are drawn to methods of increasing human growth hormone in humans that include orally administering the disclosed nutritional supplement to a healthy human being. As used herein, "healthy human being" means a human being without any physiological deficiency in hGH independent of age. Particular embodiments of the invention relate to oral administration of the disclosed nutritional supplement to a human that is at least 30 years old. The nutritional supplement may be administered from one to three times daily or, alternatively, may be administered every other day, or may be administered once a week. In particular embodiments, the nutritional supplement may be administered on an empty stomach.

[0018] In accordance with the "consist essentially of" and "consisting essentially of" language, the nutritional supplement of the third embodiments is essentially limited to the aforementioned ingredients and does not include any additional active ingredients intended to add nutritional content (e.g., vitamins, minerals, etc.), but may include additional ingredients not intended to add nutritional content such as ingredients intended to fulfill a non-nutritional purpose (e.g., coloring, fillers, flavoring, an ingredient for maintaining the structural form, etc.).

[0019] Each ingredient of the nutritional supplement of the present invention may be prepared in accordance with any method known to one of ordinary skill in the art. Alternatively, each ingredient may be obtained in a fully prepared from a commercially available source.

[0020] The nutritional supplement of the present invention may be in any suitable oral administration form, including but not limited to: a chewable form, a liquid form, a spray form, a capsule form, a suppository form, dissolvable wafer, and a powder form.

[0021] Irrespective of the structural form of the nutritional supplement, the ingredients of the nutritional supplement may be distributed homogeneously or non-homogeneously within the nutritional supplement.

[0022] The nutritional supplement of the present invention may be ingested on a regular basis, such as a daily or weekly intake at a dosage tailored to an individual's needs; i.e., the nutritional supplement is to be taken regularly as multiples (1*, 2*, etc.) of the structural units (pills, tablets, capsules, liquid dose, etc.) in accordance with the needs of the individual. For example, a senior citizen leading a sedentary life may need higher daily doses than does a young person engaged in regular strenuous exercise (e.g., a weight lifter). Alternatively, the nutritional supplement of the present invention may be ingested on an as-needed basis at a dosage tailored to the individual's needs. Medical or nutritional counseling may be beneficial for arriving at a desirable or optimal dosage tailored to the individual's needs.

[0023] The combination of types of amino acids, mass ranges, and specific formulations have been selected to be synergistically balanced and of adequate quantity to achieve the desired physiological effect, namely, growth hormone release. Improper combinations of the amino acids may be ineffective. The component amino acids are synergistic in the sense that several of them when combined together, synergistically stimulate the release of human growth hormone. The combination was also chosen to reduce or inhibit chemical combination or reaction between the amino acids.

EXAMPLES

[0024] A cross-over, placebo controlled, double-blind study involved 16 healthy subjects [12 males, 4 females; 9 Caucasian, 6 African American, 1 other; mean age=32+-14 years; body mass index=26.4+-5.0 ranging from 19.1 to 36.8 kg/m <2>]. Each subject reported to the Inpatient Unit on two occasions one week apart. After an overnight fast, subjects had an IV line placed and baseline bloods samples were drawn at -30, -15, and 0 minutes. Subjects were then asked to swallow the capsules of the test supplement or an identical looking placebo.

[0025] The administered supplement is a novel 2.9g/dose blend of 1-lysine HCl, 1-arginine HCl, oxo-proline, N-acetyl-1-cysteine, 1-glutamine, and schizonepeta (aerial parts) powder.

[0026] Blood was drawn at 15, 30, 60 and 90 and 120 minutes for assay. Human GH was measured at each time point using the Siemens Immulite 2000 (intra-assay CV was 3.72%, inter-assay CV was 5.70%, and the detection limit for GH was 0.05 ng/ml.

[0027] Mean growth hormone increased eight-fold over baseline (equivalent to 682%) after the supplement from 0.17 at baseline to 1.33 ng/ml at 120 minutes compared to a mean decrease of 52% after placebo from 0.93 to 0.45 ng/ml ( FIG. 1). The mean change in GH levels from baseline to 120 minutes (GH at 120 minutes minus GH at 0 minutes), was 1.15 (95% CI: 0.17, 2.14) ng/ml after the supplement versus -0.48 (-1.47, 0.50) ng/ml after the placebo, demonstrating a statistically significant differential effect (P=0.01). After the supplement, the mean AUC for GH across 120 minutes was 20.43 (95% CI: 19.90, 20.95) ng/ml/min which was significantly higher (P=0.04) than placebo at 19.67 (18.74, 20.59) ng/ml/min. Overall, 120 minutes after taking the supplement, GH levels were significantly higher in both absolute levels and by AUC.

[0028] Mean levels of GH reached after the subcutaneous injection of 0.06 IU of HGH in the treatment of GH deficient subjects was 0.4 ng/ml, a value that was clearly in the range of values seen in our study with oral amino acids (Janssen Y J et al. Br J Clin Pharmacol 1999;47:273-278).

[0029] The present study involved a broad range of ages and BMI's and included both genders. An additional advantage of this study of the amino-acid containing blend over previous hGH evaluations is that it contained a placebo control group and was randomized and double-blinded.


US8722114
COMPOSITIONS AND METHODS FOR INCREASING HUMAN GROWTH HORMONE LEVELS

Embodiments of the invention generally relate to methods and supplements for increasing human growth hormone (hGH) levels in healthy human beings.

TECHNICAL FIELD

[0001] Embodiments of the invention generally relate to supplements and methods for increasing human growth hormone (hGH) levels in healthy human beings.

BACKGROUND

[0002] The primary biological function of hGH includes stimulating growth, cell repair and regeneration. Once the primary growth period of adolescence concludes, the primary function of hGH in adulthood becomes that of cell regeneration and repair, helping regenerate skin, bones, heart, lungs, liver and kidneys to their optimal, youthful cell levels. As is the case with many of our other hormones or their pre-cursors, such as testosterone, oestrogen, progesterone, DHEA and melatonin, hGH levels decline with age. Therapeutically, many of these hormones can be replaced to offset some of the effects of aging such as menopausal symptoms in women or erectile dysfunction in men. The human body, like every other living entity, works on daily, or circadian, as well as monthly and annual rhythms. Daily growth hormone secretion diminishes with age with roughly half the levels at age forty that we had when we were twenty, and about one-third of those youthful levels at age sixty. In some sixty-year olds, the levels are as low as 25% of the hGH levels in a twenty-year old. Symptoms of aging include loss of muscle, increase of fat, decreased physical mobility, decreased energy levels and as a result, diminished socialization, diminished healing ability and an increased risk of cardiovascular disease and decreased life expectancy. Low hGH levels are associated with the aging process and early onset of disease. For example, Rosen and Bengtsson noted an increased death rate from cardiovascular disease in hGH deficient patients (Rosen, T., Bengtsson, B. A., Lancet 336 (1990): 285-2880).

[0003] Until recently human growth hormone (hereinafter alternatively referred to as hGH) was available only in expensive injectable forms, and benefits from the restoration of hGH levels available only to those with the ability to pay. Most recently substances that can trigger the release of human growth hormone from an individual's own anterior pituitary gland have become available. These are generically referred to as secretagogues. Secretagogues have the ability to restore hGH levels, potentially to the levels found in youth. See for reference the book entitled "Grow Young With hGH" by Dr. Ronald Klatz, President of the American Academy of Anti-Aging, published in 1997 by Harper Collins.

[0004] HGH-deficient adults have marked reductions in lean body mass, and within months of hGH treatment, gains in lean body mass, skin thickness and muscle mass are observed. (Cuneo RC et al. J Appl Physiol 1991;70:695-700; Cuneo RC et al. J Appl Physiol 1991;70:688-694; Rudman D et al. N Engl J Med 1969;280:1434-1438).

[0005] It is well-established that intravenous (IV) administration of some amino acids results in significant hGH secretion. Intravenous infusion of 183 mg of arginine/kg body weight in females increased hGH levels >20-fold and 30 g of arginine elevated serum hGH levels 8.6 fold in males (Merimee T J et al. N Engl J Med 1969;280:1434-1438; Alba-Roth J et al. J Clin Endocrinol Metab 1988;67:1186-1189). Other amino acids, such as methionine, phenylalanine, lysine, histidine, and ornithine have also led to marked increases in hGH (Alba-Roth, Muller, Schopohl, & von Werder, 1988; Chromiak & Antonio, 2002; Gourmelen, M., M. Donnadieu, et al. (1972) Ann Endocrinol (Paris) 33(5): 526-528).

[0006] Given the difficulties in IV administration of amino acids for widespread use, interest in elucidating the hGH response to oral amino acid supplements prompted testing of such supplements containing mainly arginine, lysine and ornithine at varying amounts. Yet the pronounced variability in results among these studies, which differed in aspects including subject population, supplement composition, and dosage methodologies, make clear the complexities involved in the design of an effective supplement for supporting hGH levels in the general public. (Suminski R R et al. Int J Sport Nutr 1997;7:48-60; Lambert M I et al. Int J Sport Nutr 1993;3:298-305; Corpas E et al. J Gerontol 1993;48:M128-M133; Isidori A et al. Curr Med Res Opin 1981;7:475-481; Fogelholm G M et al. Int J Sport Nutr 1993;3:290-297; Chromiak J A, Antonio J. Nutrition 2002 July;18(7-8):657-61).

[0007] Thus determination of an effective and safe oral functional blend that stimulates hGH secretion in the general population is important to determine since athletes, entertainers and now the general public seek effective hGH support supplements and understand hGH to have rejuvenating properties.

[0008] Indeed, once partial to athletes and entertainers, the desire for effective supplements to provoke growth hormone (hGH) increases now extends to the general public. Not only do they have a goal of building lean tissue and reducing fat, but also in improving skin quality and other rejuvenating qualities that hGH is understood to provide. Despite proceeding literature on oral amino acids for use in stimulating hGH, evidence for an optimized oral amino acid-containing blend able to stimulate hGH in the general public including both men and women of a wide age range is not clear.

[0009] It would be desirable to provide a nutritional supplement for elevating hGH release, in particular an amino acid-containing composition that is well tolerated having the result of increasing or elevating hGH release in those individuals whose hGH release rates have slowed as a function of increasing age or that have normal hGH levels but desire higher hGH levels. Although some existing nutritional supplements claim to impact the production of natural human growth hormone, there is a need for an improved nutritional supplement that efficiently enhances the production and effect of natural human growth hormone in the general population.

BRIEF SUMMARY OF THE INVENTION

[0010] The present invention is a nutritional supplement and method of using the same. It is a novel amino acid-containing secretagogue composition, which, taken orally, stimulates the pituitary gland to increase serum levels of hGH.

[0011] A particular embodiment of the present disclosure relates to an oral nutritional supplement that includes the amino acids 1-lysine, 1-arginine, oxo-proline, and one of either cysteine or glutamine. The amino acids may be delivered as non-toxic salts thereof, effective complexes thereof, stable chelates thereof, active esters thereof, functional derivatives thereof, and mixtures thereof which are effective to increase hGH levels in the general population.

[0012] Another particular embodiment relates to an oral nutritional supplement that consists essentially of 1-lysine HCl, 1-arginine HCl, oxo-proline, N-acetyl-1-cysteine, 1-glutamine, and schizonepeta (aerial parts) powder.

[0013] Other embodiments are drawn to methods of increasing human growth hormone in humans that include orally administering the disclosed nutritional supplement to a healthy human being.

BRIEF DESCRIPTION OF THE FIGURES

[0014] FIG. 1 shows growth hormone levels after supplement administration compared to a placebo.

DETAILED DESCRIPTION OF THE INVENTION

[0015] The present invention relates to a nutritional supplement for use by a human being. The present invention is drawn to a nutritional supplement and method of using the same. The nutritional supplement is an amino acid-containing secretagogue composition, which, taken orally, stimulates the pituitary gland to increase serum levels of hGH. Increased levels of hGH may result in inhibition of insulin depression, inhibition of hyperglycaemia and increase in insulin effectiveness, enhancement of fat conversion, lowering of cholesterol, and normalization of lipid balance. The supplement of the present invention works as a dietary supplement by assisting the body's own ability to secrete hGH naturally in a manner that is safe and effective, as well as being affordable.

[0016] A particular embodiment of the present disclosure relates to an oral nutritional supplement that includes 1-lysine, 1-arginine, oxo-proline, and one of either cysteine or glutamine. The supplement may additionally include both cysteine and glutamine and/or schizonepeta powder. In particular embodiments, a functional dosage includes the 1-arginine at a level between 0.1-6 mmol and the oxo-proline between 0.1-8 mmol, and/or the 1-lysine in an amount between 0.1-12 mmol. The cysteine and/or glutamine may be contained at a level between 0.001-6 mmol. The cysteine can be n-acetyl L-cysteine and the glutamine may be 1-glutamine. The amino acids may be delivered as non-toxic salts thereof, effective complexes thereof, stable chelates thereof, active esters thereof, functional derivatives thereof, and mixtures thereof which are effective to increase hGH levels in the general population. The nutritional supplement may be present in an amount of 2.9 grams. The nutritional supplement may be in any acceptable and known oral formulation, such as powder, tablet, capsule, liquid, or wafer form.

[0017] Another particular embodiment relates to an oral nutritional supplement that consists essentially of 1-lysine HCl, 1-arginine HCl, oxo-proline, N-acetyl-1-cysteine, 1-glutamine, and schizonepeta (aerial parts) powder. In particular embodiments, a functional dosage includes the 1-arginine HCl at a level between 0.1-6 mmol and the oxo-proline between 0.1-8 mmol, and/or the 1-lysine HCl in an amount between 0.1-12 mmol. The n-acetyl L-cysteine and/or 1-glutamine may be contained at a level between 0.001-6 mmol. In another particular embodiment, a functional dosage includes the 1-arginine HCl at a level between 2.5-4.5 mmol and the oxo-proline between 4-6 mmol, and/or the 1-lysine HCl in an amount between 7-9 mmol. The n-acetyl L-cysteine and/or 1-glutamine may be contained at a level between 0.001-0.5 mmol. The nutritional supplement may be in any acceptable and known oral formulation, such as powder, tablet, capsule, liquid, or wafer form.

[0018] Other embodiments are drawn to methods of increasing human growth hormone in humans that include orally administering the disclosed nutritional supplement to a healthy human being. As used herein, "healthy human being" means a human being without any physiological deficiency in hGH independent of age. Particular embodiments of the invention relate to oral administration of the disclosed nutritional supplement to a human that is at least 30 years old. The nutritional supplement may be administered from one to three times daily or, alternatively, may be administered every other day, or may be administered once a week. In particular embodiments, the nutritional supplement may be administered on an empty stomach.

[0019] In accordance with the "consist essentially of" and "consisting essentially Of" language, the nutritional supplement of the third embodiments is essentially limited to the aforementioned ingredients and does not include any additional active ingredients intended to add nutritional content (e.g., vitamins, minerals, etc.), but may include additional ingredients not intended to add nutritional content such as ingredients intended to fulfill a non-nutritional purpose (e.g., coloring, fillers, flavoring, an ingredient for maintaining the structural form, etc.).

[0020] Each ingredient of the nutritional supplement of the present invention may be prepared in accordance with any method known to one of ordinary skill in the art. Alternatively, each ingredient may be obtained in a fully prepared from a commercially available source.

[0021] The nutritional supplement of the present invention may be in any suitable oral administration form, including but not limited to: a chewable form, a liquid form, a spray form, a capsule form, a suppository form, dissolvable wafer, and a powder form.

[0022] Irrespective of the structural form of the nutritional supplement, the ingredients of the nutritional supplement may be distributed homogeneously or non-homogeneously within the nutritional supplement.

[0023] The nutritional supplement of the present invention may be ingested on a regular basis, such as a daily or weekly intake at a dosage tailored to an individual's needs; i.e., the nutritional supplement is to be taken regularly as multiples (2*, 2*, etc.) of the structural units (pills, tablets, capsules, liquid dose, etc.) in accordance with the needs of the individual. For example, a senior citizen leading a sedentary life may need higher daily doses than does a young person engaged in regular strenuous exercise (e.g., a weight lifter). Alternatively, the nutritional supplement of the present invention may be ingested on an as-needed basis at a dosage tailored to the individual's needs. Medical or nutritional counseling may be beneficial for arriving at a desirable or optimal dosage tailored to the individual's needs.

[0024] The combination of types of amino acids, mass ranges, and specific formulations have been selected to be synergistically balanced and of adequate quantity to achieve the desired physiological effect, namely, growth hormone release. Improper combinations of the amino acids may be ineffective. The component amino acids are synergistic in the sense that several of them when combined together, synergistically stimulate the release of human growth hormone. The combination was also chosen to reduce or inhibit chemical combination or reaction between the amino acids.

EXAMPLES

[0025] A cross-over, placebo controlled, double-blind study involved 16 healthy subjects [12 males, 4 females; 9 Caucasian, 6 African American, 1 other; mean age=32+-14 years; body mass index=26.4+-5.0 ranging from 19.1 to 36.8 kg/m <2>]. Each subject reported to the Inpatient Unit on two occasions one week apart. After an overnight fast, subjects had an IV line placed and baseline bloods samples were drawn at -30, -15, and 0 minutes. Subjects were then asked to swallow the capsules of the test supplement or an identical looking placebo.

[0026] The administered supplement is a novel 2.9 g/dose blend of 1-lysine HCl, 1-arginine HCl, oxo-proline, N-acetyl-1-cysteine, 1-glutamine, and schizonepeta (aerial parts) powder.

[0027] Blood was drawn at 15, 30, 60 and 90 and 120 minutes for assay. Human GH was measured at each time point using the Siemens Immulite 2000 (intra-assay CV was 3.72%, inter-assay CV was 5.70%, and the detection limit for GH was 0.05 ng/ml.

[0028] Mean growth hormone increased eight-fold over baseline (equivalent to 682%) after the supplement from 0.17 at baseline to 1.33 ng/ml at 120 minutes compared to a mean decrease of 52% after placebo from 0.93 to 0.45 ng/ml ( FIG. 1). The mean change in GH levels from baseline to 120 minutes (GH at 120 minutes minus GH at 0 minutes), was 1.15 (95% CI: 0.17, 2.14) ng/ml after the supplement versus -0.48 (-1.47, 0.50) ng/ml after the placebo, demonstrating a statistically significant differential effect (P=0.01). After the supplement, the mean AUC for GH across 120 minutes was 20.43 (95% CI: 19.90, 20.95) ng/ml/min which was significantly higher (P=0.04) than placebo at 19.67 (18.74, 20.59) ng/ml/min. Overall, 120 minutes after taking the supplement, GH levels were significantly higher in both absolute levels and by AUC.

[0029] Mean levels of GH reached after the subcutaneous injection of 0.06 IU of HGH in the treatment of GH deficient subjects was 0.4 ng/ml, a value that was clearly in the range of values seen in our study with oral amino acids (Janssen Y J et al. Br J Clin Pharmacol 1999;47:273-278).

[0030] The present study is distinct in that it had a broad range of ages and BMF s and included both genders. An additional advantage of this study of the novel amino-acid containing blend over previous hGH evaluations is that it contained a placebo control group and was randomized and double-blinded.


http://wafflesatnoon.com/serovital-hgh-side-effects/

The purpose of this article is to evaluate possible side effects of Serovita-hgh. Not everyone experiences side effects.

The active ingredients of Serovital-hgh are:

L-Lysine HCI
L-Arginine HCI
Oxo-Proline
N-Acrtyl L-Cysteine
L-Glutamine
Schizonepeta (aerial parts) powder

The potential side effects of these individual ingredients will help give us a better idea of the possible side effects of Serovital-hgh as a whole. The following ingredients have known possible side effects:

L-Lysine HCI – Stomach pain, diarrhea. Avoid taking large amounts of calcium and lysine at the same time.
L-Arginine HCI – Abdominal pain, bloating, diarrhea, gout, allergies, worsening of asthma, low blood pressure, allergic reaction, hives, increased risk of bleeding.
N-Acrtyl L-Cysteine - Nausea, vomiting, diarrhea, constipation.


http://accroya.com/my-serovital-hgh-experience/
November 22, 2013

My Experience with Serovital-hgh
by James White

I remember hearing about Sylvester Stallone's use of human growth hormone (HGH), and realized how dang good he still looks at nearly 70 years old. Although I've been reluctant to go the HGH route, I recently heard of a product that supposedly helps your body boost hgh, called Serovital-hgh. Here are my thoughts and experiences with the product.

So I decided to plunk down a C-Note for a month supply. I went through a local Sephora located inside a JC Penney here in Southern Nevada.

I wasn’t even sure at first what it was – a pill, a cream, something else? (It’s a pill) I can see a fancy cream making me look decades younger, but a pill?

Anyway, I tried Serovital-hgh for a month, following the instructions exactly as stated – taking it in the morning two hours before eating breakfast.

After a month… well, I can’t say I noticed much. Actually I noticed nothing at all. No side effects, and no benefits.

Better at Night?

A gym rat friend of mine said that it would probably work better taking it at night rather than in the morning, even though Serovital’s website says you can take it either time. I wonder if this is why it works for some people and not others?

Competition

I should point out that Serovital isn’t the only game in town when it comes to HGH boosters. Take a look at Fountain of Youth HGH Complete, which contains many of the ingredients of Serovital – and actually quite a few more. Its cost? $40.

It’s hard not to browse the web without eventually seeing an ad for Serovital-hgh. Well, maybe that’s just me, because I Google a lot of anti-aging stuff, and I know Google delivers ads based on search history. OK, so it’s hard for ME not to browse the internet without seeing ads for Serovital.

What is Serovital-hgh?

The website claims to be a blend of amino acids which raises growth hormone in the body. It is not human growth hormone.

How much does Serovital-hgh Cost?

It ain’t cheap at about $100 for a month supply. Buy it somewhere local, such as Ulta. At least that way you can save yourself the $7 shipping they want to charge, plus the week or so it will take to arrive.

Another reason I suggest picking it up at Ulta is because the official website (serovital.com) wants to automatically bill you every month to keep replenishing your supply.

The Catch

The website admits there are three “catches” to using the product:

You have to use it alongside a sensible diet and exercise regimen. That probably excludes half of the potential customers right there.
It has to be taken on an empty stomach. Easy enough.
It’s cheaper than HGH injections, but will still cost about $100 a month. Youthful vigor is apparently only for the rich.

One more “catch” they don’t really advertise is that you have to use it for about 2 months to even begin to notice any results.


http://www.hghsupplement.net/serovital-hgh/

SeroVital HGH Review

By: vagueswoosh
February 13, 2013

A lot of people fantasize about life when they were 10 years younger.

And while you can’t go back in time, Sierra Research Labs, like so many other supplement companies, says you can get your body back by increasing HGH levels, specifically they want you to believe you can do it with SeroVital HGH.

SeroVital HGH is an HGH releaser, which means it uses natural ingredients like other HGH supplements to increase human growth hormone levels.

Today, there are clear indications increasing HGH can provide numerous benefits including:

• Reduced body fat
• Increased lean muscle mass
• Strengthened bones
• Improved energy levels
• Diminished wrinkles
• Heightened sex drive
• Improved mood

SeroVital HGH advertising echoes these benefits, which you would expect. However, it’s down to the SeroVital HGH formula to actually increase HGH enough to deliver them. After taking some time to look at some studies on SeroVital’s formula, I was curious if SeroVital HGH was strong enough to get the job done, so I looked into the product further.

What’s in SeroVital HGH?

Since everything hinges on the SeroVital HGH formula, let’s start there.

Sierra Research Lab doesn’t tell us anything about their formula on their website. To discover that information, I had to look elsewhere. Luckily, SeroVital HGH retails on Ulta.com as well. According to Ulta, SeroVital HGH contains:

L-Lysine – L-lysine is the first in a long line of amino acids in SeroVital. Lysine produces hormones that trigger greater HGH release from the pituitary gland. Because lysine isn’t naturally-produced, you’ll need adequate levels from your diet. With the extra lysine in SeroVital, your HGH production should increase.

L-Arginine – Arginine is an amino acid that increases HGH levels as well as widens blood vessels to facilitate HGH circulation. It works especially well when combined with lysine. In a 1997 study, subjects who took arginine and lysine say significant increases in HGH circulation [1].

Oxo-Proline – Also known as pyroglutamic acid, oxo-proline is an amino acid with antioxidant properties. It’s also used to moisturize skin. This provides some anti-aging benefits, but does nothing to directly increase growth hormone levels.

N-Acetyl L-Cysteine (NAC) – NAC is a modified cysteine molecule. Like oxo-proline, it has a high antioxidant count. These antioxidants boost the immune system and improve health, but do nothing to raise HGH levels. However, when NAC is metabolized, it produces glutathione. Glutathione in turn increases DHEA and IGF-1 levels, which promote greater HGH release [2].

L-Glutamine – L-glutamine is the last amino acid in SeroVital and among the most powerful. Glutamine raises circulating HGH levels within 90 minutes of ingestion, according to one study [3]. It also prevents muscle breakdown, maintaining good body composition.

Schizonepta Powder – Rounding out the formula is the herbal extract schizonepta. Schizonepta treats inflammation, but no evidence suggests it promotes greater HGH release.

The amino acids in SeroVital are good ones, but they’re also commonplace. You can get these from your diet if you take care. Furthermore, there’s no ingredient information to judge whether the formula includes recommended quantities for each amino acid.

Sierra Research claims this formula is backed by a clinical study, but the study is not peer-reviewed or printed in a scientific journal.

If I had to guess, I’d say SeroVital is no more effective than your average HGH releaser.

Can SeroVital Cause Side Effects?

Another concern many people have with HGH formulas is side effect risk. While all ingredients in SeroVital are natural and non-stimulating, excessive amino acid intake can cause a few problems. Specifically, arginine and glutamine can cause:

• Bloating
• Water retention
• Nausea
• Abdominal pain
• Diarrhea

Of course, without information on ingredient quantity, I can’t be sure if these side effects will be severe or if they will be present at all. Just be aware that they’re a possibility.

How Much Does SeroVital Cost?

If SeroVital sounds like something you want to try, you can find it at SeroVital.com for $99.99 or at Ulta.com for $89.99. It’s also available from other retailers like Lucky Vitamin, but all prices stay within this range.

Although this is significantly cheaper than growth hormone injections, this price still stings. You’ll likely need more than a 1-month supply to see the full benefits, which means you’ll be shelling out $100 every month for an indeterminate period of time.

Is There a SeroVital Guarantee?

Sometimes a money-back guarantee reassures customers and makes the price tag more palatable. While SeroVital HGH advertises a “100% money-back guarantee,” there is no additional information on the website or elsewhere online.

If you’re unsatisfied with SeroVital HGH, you may need to contact the company at 1-800-435-1409 and request more information about the refund. Most refunds cover only the first 30 to 90 days of purchase, so don’t put it off.

Is SeroVital Worth a Try?

SeroVital HGH has gotten a lot of press, but I’m not sure it deserves it. With a sketchy backing trial and guarantee, an expensive price, and commonplace ingredients, I don’t see anything spectacular about this product. I’d recommend looking elsewhere before trying SeroVital.

References

[1] Suminski, R.R., R.J. Robertson, F.L. Goss, S. Arslanian, J. Kang, S. DaSilva, A.C. Utter, and K.F. Metz. 1997. Acute effect of amino acid ingestion and resistance exercise on plasma growth hormone concentration in young men. International Journal of Sports Nutrition: Vol. 7, Issue 1.

[2] Keller, Rob. Glutathione: Max Health for Life. Accessed from http://maxhealthforlife.net/.

[3] Welbourne, T.C. 1995. Increased plasma bicarbonate and growth hormone after an oral glutamine load. American Journal of Clinical Nutrition. Vol. 61, Issue 5.
HGHSupps' #1 HGH Supplement of 2014


http://www.secratatropinhgh.com/

Secratatropin HGH is the most powerful HGH booster that's ever been available. If you're serious about increasing HGH, nothing beats the 100% GUARANTEED Secratatropin HGH.

All-Natural HGH Complex

Secratatropin is an all-natural HGH complex that contains 7 different amino acids and other powerful ingredients including Alpha GPC, GABA, Tribulus Terristris and more. With over 3600mg per serving, your satisfaction is guaranteed or your money back. Secratatropin is made with 100% safe and natural ingredients to help you achieve your goals.



Radionuclide Removal by Zeolite

SURFACE-COATED ZEOLITE PARTICLE AND CESIUM REMOVING MATERIAL CONTAINING THE SAME
JP2014018734

METHOD FOR SEPARATION, STABILIZATION AND IMMOBILIZATION OF MULTI-NUCLIDE ELEMENTS INCLUDING CESIUM AND STRONTIUM
WO2014010638

RADIOACTIVE CESIUM-ADSORBING FIBER AND MANUFATURING METHOD THEREFOR AS WELL AS DEVICE FOR DETECTING RADIOACTIVE CESIUM CONCENTRATION IN WATER USING RADIOACTIVE CESIUM-ADSORBING FIBER
WO2013187505

ZEOLITE AND MANUFACTURING METHOD THEREOF, AND METHOD FOR SELECTIVE AND SPECIFIC CAPTURE OF CESIUM
WO2013150851

Filter medium for removing radioactive cobalt and cesium in water and preparation method thereof
CN103341287

METHOD FOR REMOVING RADIOACTIVE CESIUM, HYDROPHILIC RESIN COMPOSITION FOR REMOVING RADIOACTIVE CESIUM, METHOD FOR REMOVING RADIOACTIVE IODINE AND RADIOACTIVE CESIUM, AND HYDROPHILIC RESIN COMPOSITION FOR REMOVING RADIOACTIVE IODINE AND RADIOACTIVE CESIUM
WO2013108892

METHOD AND AGENT FOR ELIMINATION OF DEPOSITED IODINE, CESIUM, STRONTIUM RADIONUCLIDES
RU2484833

METHOD FOR REMOVING RADIOACTIVE CESIUM FROM AQUEOUS SOLUTION CONTAINING RADIOACTIVE CESIUM
JP2013117450

DECONTAMINATION METHOD FOR REMOVING RADIOACTIVE CESIUM FROM INCINERATED ASH OR FLY ASH CONTAINING RADIOACTIVE CESIUM
JP2013101098

STORAGE METHOD FOR CONTAMINANT BY RADIOACTIVE CESIUM AND STORAGE CONTAINER FOR CONTAMINANT BY RADIOACTIVE CESIUM
JP2013101094

WATER PURIFICATION FILTER CARTRIDGE FOR CESIUM REMOVAL AND METHOD OF MANUFACTURING THE SAME
JP2013088411

DECONTAMINATION METHOD OF POLLUTED WATER, DECONTAMINATION METHOD OF CONTAMINATED SOIL, AND DECONTAMINATION ADSORBENT FOR POLLUTED WATER AND CONTAMINATED SOIL
JP2013079846

PROCESSING METHOD OF RADIOACTIVITY WASTE USING RYUKYUS LIMESTONE
JP2013068484

METHOD OF REMOVING METAL COMPONENT, AND SUBSTANCE USED FOR THE SAME
JP2013064694

METHOD FOR PROCESSING RADIOACTIVE CONTAMINATED WATER
JP2013057599

WATER PURIFIER FOR REMOVING RADIOACTIVE MATERIAL FROM TAP WATER
JP2013007634

PURIFICATION (DECONTAMINATION) METHOD OF DRAINAGE (WASTE WATER)/SOIL CONTAINING CESIUM AND HEAVY METALS BY NEONITE
JP2013003130

System for treating overproof radioactive laundry waste water
CN102930912

METHOD FOR DECONTAMINATING DRINKING WATER CONTAMINATED BY RADIOACTIVE SUBSTANCE, DRINKING WATER PURIFICATION DEVICE, AND INTERNALLY CLEANSING DRINKING WATER
WO2012165026

Preparation method for strontium-cesium co-solidified body
CN102208223

METHOD FOR ISOLATING NUCLEIC ACID FROM SOLUTION CONTAINING CESIUM CHLORIDE AND ETHIDIUM BROMIDE
JP2009082105

Back filling material for disposing radioactive waste and preparation method thereof
CN101303907

Method to synthesize dense crystallized sodalite pellet for immobilizing halide salt radioactive waste
US5340506

Method for aqueous radioactive waste treatment
US5298166

Method for primary containment of cesium wastes
US4376792

Process for producing zeolite adsorbent and process for treating radioactive liquid waste with the zeolite adsorbent
US4448711

ZEOLITE-BASED ORGANOMINERAL SORBENT AND A METHOD FOR PREPARATION THEREOF
RU2284857

INTEGRATED PROCESSING OF LIQUID RADIOACTIVE WASTES
RU2118945

METHOD FOR RECOVERY OF LIQUID RADIOACTIVE WASTES
RU2112289

MANUFACTURE OF SINTERED SOLIDIFIED BODY CONTAINING CESIUM AND/OR STRONTIUM BEING RADIOISOTOPE AND METHOD FOR USING IT AS LARGE-SCALE RI BATTERY THROUGH PROCESSING
JPH06138298

ELUTION OF RADIOACTIVE NUCLIDE FROM USED ION EXCHANGE RESIN
JPS6491096
   
SEPARATING METHOD FOR CESIUM IN WATER SOLUTION OF URANIUM
JPH04340497

METHOD FOR REMOVING RADIOACTIVE CESIUM IN URANIUM SOLUTION
JPH04315998

Process and device for separating cesium, strontium and transuranium elements from a soda effluent by precipitating out the various elements using insolubility agents such as TPB- for the cesium
FR2805758

Apparatus and method for removing strontium and/or cesium ions from an aqueous solution containing chemical hardness.
EP0243557

Borosilicate zeolite for nuclear waste disposal.
EP0180308
 


http://www.orthodoxytoday.org/articles/SolhenitsynLies.php?/articles/SolhenitsynLies.htm

Live Not By Lies

by

Alexander Solzhenitsyn

 
Solzhenitsyn penned this essay in 1974 and it circulated among Moscow's intellectuals at the time. It is dated Feb. 12, the same day that secret police broke into his apartment and arrested him. The next day he was exiled to West Germany. The essay is a call to moral courage and serves as light to all who value truth.

At one time we dared not even to whisper. Now we write and read samizdat, and sometimes when we gather in the smoking room at the Science Institute we complain frankly to one another: What kind of tricks are they playing on us, and where are they dragging us? Gratuitous boasting of cosmic achievements while there is poverty and destruction at home. Propping up remote, uncivilized regimes. Fanning up civil war. And we recklessly fostered Mao Tse-tung at our expense—and it will be we who are sent to war against him, and will have to go. Is there any way out? And they put on trial anybody they want and they put sane people in asylums—always they, and we are powerless.

Things have almost reached rock bottom. A universal spiritual death has already touched us all, and physical death will soon flare up and consume us both and our children—but as before we still smile in a cowardly way and mumble without tounges tied. But what can we do to stop it? We haven't the strength?

We have been so hopelessly dehumanized that for today's modest ration of food we are willing to abandon all our principles, our souls, and all the efforts of our predecessors and all opportunities for our descendants—but just don't disturb our fragile existence. We lack staunchness, pride and enthusiasm. We don't even fear universal nuclear death, and we don't fear a third world war. We have already taken refuge in the crevices. We just fear acts of civil courage.

We fear only to lag behind the herd and to take a step alone-and suddenly find ourselves without white bread, without heating gas and without a Moscow registration.

We have been indoctrinated in political courses, and in just the same way was fostered the idea to live comfortably, and all will be well for the rest of our lives. You can't escape your environment and social conditions. Everyday life defines consciousness. What does it have to do with us? We can't do anything about it?

But we can—everything. But we lie to ourselves for assurance. And it is not they who are to blame for everything—we ourselves, only we. One can object: But actually toy can think anything you like. Gags have been stuffed into our mouths. Nobody wants to listen to us and nobody asks us. How can we force them to listen? It is impossible to change their minds.

It would be natural to vote them out of office—but there are not elections in our country. In the West people know about strikes and protest demonstrations—but we are too oppressed, and it is a horrible prospect for us: How can one suddenly renounce a job and take to the streets? Yet the other fatal paths probed during the past century by our bitter Russian history are, nevertheless, not for us, and truly we don't need them.

Now that the axes have done their work, when everything which was sown has sprouted anew, we can see that the young and presumptuous people who thought they would make out country just and happy through terror, bloody rebellion and civil war were themselves misled. No thanks, fathers of education! Now we know that infamous methods breed infamous results. Let our hands be clean!

The circle—is it closed? And is there really no way out? And is there only one thing left for us to do, to wait without taking action? Maybe something will happen by itself? It will never happen as long as we daily acknowledge, extol, and strengthen—and do not sever ourselves from the most perceptible of its aspects: Lies.

When violence intrudes into peaceful life, its face glows with self-confidence, as if it were carrying a banner and shouting: “I am violence. Run away, make way for me—I will crush you.” But violence quickly grows old. And it has lost confidence in itself, and in order to maintain a respectable face it summons falsehood as its ally—since violence lays its ponderous paw not every day and not on every shoulder. It demands from us only obedience to lies and daily participation in lies—all loyalty lies in that.

And the simplest and most accessible key to our self-neglected liberation lies right here: Personal non-participation in lies. Though lies conceal everything, though lies embrace everything, but not with any help from me.

This opens a breach in the imaginary encirclement caused by our inaction. It is the easiest thing to do for us, but the most devastating for the lies. Because when people renounce lies it simply cuts short their existence. Like an infection, they can exist only in a living organism.

We do not exhort ourselves. We have not sufficiently matured to march into the squares and shout the truth our loud or to express aloud what we think. It's not necessary.

It's dangerous. But let us refuse to say that which we do not think.

This is our path, the easiest and most accessible one, which takes into account out inherent cowardice, already well rooted. And it is much easier—it's dangerous even to say this—than the sort of civil disobedience which Gandhi advocated.

Our path is to talk away fro the gangrenous boundary. If we did not paste together the dead bones and scales of ideology, if we did not sew together the rotting rags, we would be astonished how quickly the lies would be rendered helpless and subside.

That which should be naked would then really appear naked before the whole world.

So in our timidity, let each of us make a choice: Whether consciously, to remain a servant of falsehood—of course, it is not out of inclination, but to feed one's family, that one raises his children in the spirit of lies—or to shrug off the lies and become an honest man worthy of respect both by one's children and contemporaries.

And from that day onward he:

Will not henceforth write, sign, or print in any way a single phrase which in his opinion distorts the truth.

Will utter such a phrase neither in private conversation not in the presence of many people, neither on his own behalf not at the prompting of someone else, either in the role of agitator, teacher, educator, not in a theatrical role.

Will not depict, foster or broadcast a single idea which he can only see is false or a distortion of the truth whether it be in painting, sculpture, photography, technical science, or music.

Will not cite out of context, either orally or written, a single quotation so as to please someone, to feather his own nest, to achieve success in his work, if he does not share completely the idea which is quoted, or if it does not accurately reflect the matter at issue.

Will not allow himself to be compelled to attend demonstrations or meetings if they are contrary to his desire or will, will neither take into hand not raise into the air a poster or slogan which he does not completely accept.

Will not raise his hand to vote for a proposal with which he does not sincerely sympathize, will vote neither openly nor secretly for a person whom he considers unworthy or of doubtful abilities.

Will not allow himself to be dragged to a meeting where there can be expected a forced or distorted discussion of a question. Will immediately talk out of a meeting, session, lecture, performance or film showing if he hears a speaker tell lies, or purvey ideological nonsense or shameless propaganda.

Will not subscribe to or buy a newspaper or magazine in which information is distorted and primary facts are concealed. Of course we have not listed all of the possible and necessary deviations from falsehood. But a person who purifies himself will easily distinguish other instances with his purified outlook.

No, it will not be the same for everybody at first. Some, at first, will lose their jobs. For young people who want to live with truth, this will, in the beginning, complicate their young lives very much, because the required recitations are stuffed with lies, and it is necessary to make a choice.

But there are no loopholes for anybody who wants to be honest. On any given day any one of us will be confronted with at least one of the above-mentioned choices even in the most secure of the technical sciences. Either truth or falsehood: Toward spiritual independence or toward spiritual servitude.

And he who is not sufficiently courageous even to defend his soul—don't let him be proud of his “progressive” views, don't let him boast that he is an academician or a people's artist, a merited figure, or a general—let him say to himself: I am in the herd, and a coward. It's all the same to me as long as I'm fed and warm.

Even this path, which is the most modest of all paths of resistance, will not be easy for us. But it is much easier than self-immolation or a hunger strike: The flames will not envelope your body, your eyeballs, will not burst from the heat, and brown bread and clean water will always be available to your family.

A great people of Europe, the Czechoslovaks, whom we betrayed and deceived: Haven't they shown us how a vulnerable breast can stand up even against tanks if there is a worthy heart within it?

You say it will not be easy? But it will be easiest of all possible resources. It will not be an easy choice for a body, but it is the only one for a soul. Not, it is not an easy path. But there are already people, even dozens of them, who over the years have maintained all these points and live by the truth.

So you will not be the first to take this path, but will join those who have already taken it. This path will be easier and shorter for all of us if we take it by mutual efforts and in close rank. If there are thousands of us, they will not be able to do anything with us. If there are tens of thousands of us, then we would not even recognize our country.

If we are too frightened, then we should stop complaining that someone is suffocating us. We ourselves are doing it. Let us then bow down even more, let us wail, and out brothers the biologists will help to bring nearer the day when they are able to read our thoughts are worthless and hopeless.

And if we get cold feet, even taking this step, then we are worthless and hopeless, and the scorn of Pushkin should be directed to us:

Why should cattle have the gifts of freedom?

Their heritage from generation to generation is the belled yoke and the lash.



http://www.nature.com/neuro/journal/v17/n6/full/nn.3719.html
Nature Neuroscience17, 810–812 (2014)
doi:10.1038/nn.3719
11 May 2014

Induction of self awareness in dreams through frontal low current stimulation of gamma activity

Ursula Voss, Romain Holzmann, Allan Hobson, Walter Paulus, Judith Koppehele-Gossel, Ansgar Klimke & Michael A Nitsche   

Recent findings link fronto-temporal gamma electroencephalographic (EEG) activity to conscious awareness in dreams, but a causal relationship has not yet been established. We found that current stimulation in the lower gamma band during REM sleep influences ongoing brain activity and induces self-reflective awareness in dreams. Other stimulation frequencies were not effective, suggesting that higher order consciousness is indeed related to synchronous oscillations around 25 and 40 Hz.






http://phys.org/news/2014-08-scientists-splitter-ordinary-aaa-battery.html
Aug 22, 2014

Scientists develop a water splitter that runs on an ordinary AAA battery

In 2015, American consumers will finally be able to purchase fuel cell cars from Toyota and other manufacturers. Although touted as zero-emissions vehicles, most of the cars will run on hydrogen made from natural gas, a fossil fuel that contributes to global warming.

Now scientists at Stanford University have developed a low-cost, emissions-free device that uses an ordinary AAA battery to produce hydrogen by water electrolysis. The battery sends an electric current through two electrodes that split liquid water into hydrogen and oxygen gas. Unlike other water splitters that use precious-metal catalysts, the electrodes in the Stanford device are made of inexpensive and abundant nickel and iron.

"Using nickel and iron, which are cheap materials, we were able to make the electrocatalysts active enough to split water at room temperature with a single 1.5-volt battery," said Hongjie Dai, a professor of chemistry at Stanford. "This is the first time anyone has used non-precious metal catalysts to split water at a voltage that low. It's quite remarkable, because normally you need expensive metals, like platinum or iridium, to achieve that voltage."

In addition to producing hydrogen, the novel water splitter could be used to make chlorine gas and sodium hydroxide, another important industrial chemical, according to Dai. He and his colleagues describe the new device in a study published in the Aug. 22 issue of the journal Nature Communications.

The promise of hydrogen

Automakers have long considered the hydrogen fuel cell a promising alternative to the gasoline engine. Fuel cell technology is essentially water splitting in reverse. A fuel cell combines stored hydrogen gas with oxygen from the air to produce electricity, which powers the car. The only byproduct is water – unlike gasoline combustion, which emits carbon dioxide, a greenhouse gas.

Earlier this year, Hyundai began leasing fuel cell vehicles in Southern California. Toyota and Honda will begin selling fuel cell cars in 2015. Most of these vehicles will run on fuel manufactured at large industrial plants that produce hydrogen by combining very hot steam and natural gas, an energy-intensive process that releases carbon dioxide as a byproduct.

Stanford graduate student Ming Gong (left) and Professor Hongjie Dai

 


Splitting water to make hydrogen requires no fossil fuels and emits no greenhouse gases. But scientists have yet to develop an affordable, active water splitter with catalysts capable of working at industrial scales.

"It's been a constant pursuit for decades to make low-cost electrocatalysts with high activity and long durability," Dai said. "When we found out that a nickel-based catalyst is as effective as platinum, it came as a complete surprise."

Saving energy and money

The discovery was made by Stanford graduate student Ming Gong, co-lead author of the study. "Ming discovered a nickel-metal/nickel-oxide structure that turns out to be more active than pure nickel metal or pure nickel oxide alone," Dai said. "This novel structure favors hydrogen electrocatalysis, but we still don't fully understand the science behind it."

The nickel/nickel-oxide catalyst significantly lowers the voltage required to split water, which could eventually save hydrogen producers billions of dollars in electricity costs, according to Gong. His next goal is to improve the durability of the device.

"The electrodes are fairly stable, but they do slowly decay over time," he said. "The current device would probably run for days, but weeks or months would be preferable. That goal is achievable based on my most recent results."

The researchers also plan to develop a water splitter than runs on electricity produced by solar energy.

"Hydrogen is an ideal fuel for powering vehicles, buildings and storing renewable energy on the grid," said Dai. "We're very glad that we were able to make a catalyst that's very active and low cost. This shows that through nanoscale engineering of materials we can really make a difference in how we make fuels and consume energy."



http://www.bbc.com/news/health-28834058
18 August 2014

Hair loss reversed in alopecia areata sufferers

by

Smitha Mundasad
Health reporter, BBC News

Alopecia can lead to patchy or complete hair-loss People saw their hair fully restored after just five months of treatment

Scientists have completely reversed hair loss in three people by giving them a drug normally used to treat bone marrow disorders.

The patients had alopecia areata - a condition that can cause severe, patchy baldness that is difficult to treat.

But after five months of taking the medication ruxolitinib, all three saw total hair re-growth.

The findings from Columbia University Medical Center are published in the journal Nature Medicine.

'Devastating disease'

Alopecia areata affects around two in every 1,000 people in the UK and is thought to be caused by the immune system attacking hair follicles.

The US scientists had previously identified a set of immune cells involved in the destruction of hair and conducted a number of successful trials in mice.

They then gave three patients with moderate to severe alopecia areata a twice daily dose of ruxolitinib.

This medication is already approved for use in bone marrow conditions in the United States and European Union.

All three patients had lost at least a third of their hair but saw dramatic hair growth within five months of therapy.

Lead researcher Dr Raphael Clynes said: "We've only begun testing the drug in patients, but if the drug continues to be successful and safe, it will have a dramatic positive impact on the lives of people with the disease."

Prof David Bickers, a dermatologist at Columbia University who has treated many patients with the disease, said: "There are few tools in the arsenal for the treatment of alopecia areata that have any demonstrated efficacy.

"This is a major step forward in improving the standard of care for patients suffering from this devastating disease."

Researchers say more work is now needed to see if the drug can be offered more widely.

Alopecia areata can occur at any age but is most often seen in teenagers and young adults.

It is not related to the more common male-pattern hair loss that is thought to be driven by hormones.

Scientists say as the mechanisms behind this condition are different, the therapy is less likely to prove effective for this more common problem.

Patents

Methods for Treating Hair Loss Disorders
US2014065153 // WO2013149194 // WO2012061536
The invention provides for methods for treating a hair loss disorder in a subject by administering a JAK/STAT inhibitor

METHODS FOR DETECTING AND REGULATING ALOPECIA AREATA AND GENE COHORTS THEREOF
US2013078244


http://en.wikipedia.org/wiki/Ruxolitinib

Ruxolitinib

(3R)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrazol-1-yl]propanenitrile
Trade names     Jakafi, Jakavi
CAS number     941678-49-5 Yes
ATC code     L01XE18
ChemSpider     25027389 Yes
UNII     82S8X8XX8H Yes
ChEMBL     CHEMBL1789941
Synonyms     INCB018424, INC424

Ruxolitinib (INC424, INCB18424, trade names Jakafi and Jakavi, by Incyte Pharmaceuticals and Novartis) is a drug for the treatment of intermediate or high-risk myelofibrosis, a type of bone marrow cancer.[2][3] It is also being investigated for the treatment of other types of cancer (such as lymphomas and pancreatic cancer),[4] for polycythemia vera,[4] for plaque psoriasis, and for alopecia areata [5].

The phase III Controlled Myelofibrosis Study with Oral JAK Inhibitor-I (COMFORT-I) and COMFORT-II trials showed significant benefits by reducing spleen size, relieving debilitating symptoms, and improving overall survival.[6][7][8][9]

Mechanism of action

Ruxolitinib is a Janus kinase inhibitor with selectivity for subtypes JAK1 and JAK2 of this enzyme.[10][11] Ruxolitinib inhibits dysregulated JAK signaling associated with myelofibrosis. JAK1 and JAK2 recruit signal transducers and activators of transcription (STATs) to cytokine receptors leading to modulation of gene expression.
Side effects

Immunologic side effects have included herpes zoster (shingles) (1.9%) and case reports of opportunistic infections.[12] Metabolic side effects have included weight gain (7.1%). Laboratory abnormalities have included alanine transaminase (ALT) abnormalities (25.2%), aspartate transaminase (AST) abnormalities (17.4%), and elevated cholesterol levels (16.8%).[citation needed]

Legal status

In November 2011, ruxolitinib was approved by the U.S. Food and Drug Administration (FDA) for the treatment of intermediate or high-risk myelofibrosis based on results of the COMFORT-I and COMFORT-II Trials.[13]

Economics

Some analysts believe this to be a potential blockbuster drug.[4] As of the end of March 2012, and according to an Incyte spokesman, approximately 1000 physicians had prescribed the drug in the United States, out of a total 6500 hematologists and oncologists nationwide.[4]

References

"Jakafi (ruxolitinib) dosing, indications, interactions, adverse effects, and more". Medscape Reference. WebMD

Mesa, Ruben A.; Yasothan, Uma; Kirkpatrick, Peter (2012). "Ruxolitinib". Nature Reviews Drug Discovery 11 (2): 103–4. doi:10.1038/nrd3652. PMID 22293561.

Harrison, C; Mesa, R; Ross, D; Mead, A; Keohane, C; Gotlib, J; Verstovsek, S (2013). "Practical management of patients with myelofibrosis receiving ruxolitinib". Expert Review of Hematology 6 (5): 511–23. doi:10.1586/17474086.2013.827413. PMID 24083419.

Natoli, Cori Anne (May 5, 2012), "Incyte looks to ride on drug's success", The News Journal,

Xing, Luzhou et al (2014). "Letter, Alopecia areata is driven by cytotoxic T lymphocytes and is reversed by JAK inhibition". Nature Medicine. doi:10.1038/nm.3645.

Harrison, C.; Kiladjian, J. J.; Al-Ali, H. K.; Gisslinger, H.; Waltzman, R.; Stalbovskaya, V.; McQuitty, M.; Hunter, D. S.; Levy, R.; Knoops, L.; Cervantes, F.; Vannucchi, A. M.; Barbui, T.; Barosi, G. (2012). "JAK Inhibition with Ruxolitinib versus Best Available Therapy for Myelofibrosis". New England Journal of Medicine 366 (9): 787–798. doi:10.1056/NEJMoa1110556. PMID 22375970.

Verstovsek, S.; Mesa, R. A.; Gotlib, J.; Levy, R. S.; Gupta, V.; Dipersio, J. F.; Catalano, J. V.; Deininger, M.; Miller, C.; Silver, R. T.; Talpaz, M.; Winton, E. F.; Harvey Jr, J. H.; Arcasoy, M. O.; Hexner, E.; Lyons, R. M.; Paquette, R.; Raza, A.; Vaddi, K.; Erickson-Viitanen, S.; Koumenis, I. L.; Sun, W.; Sandor, V.; Kantarjian, H. M. (2012). "A Double-Blind, Placebo-Controlled Trial of Ruxolitinib for Myelofibrosis". New England Journal of Medicine 366 (9): 799–807. doi:10.1056/NEJMoa1110557. PMID 22375971.

Tefferi, A. (2012). "Challenges Facing JAK Inhibitor Therapy for Myeloproliferative Neoplasms". New England Journal of Medicine 366 (9): 844–846. doi:10.1056/NEJMe1115119. PMID 22375977.

ASCO Annual Meeting 2011: JAK Inhibitor Ruxolitinib Demonstrates Significant Clinical Benefit in Myelofibrosis

Mesa, RA (2010). "Ruxolitinib, a selective JAK1 and JAK2 inhibitor for the treatment of myeloproliferative neoplasms and psoriasis". IDrugs : the investigational drugs journal 13 (6): 394–403. PMID 20506062.

Pardanani, A.; Tefferi, A. (2011). "Targeting myeloproliferative neoplasms with JAK inhibitors". Current Opinion in Hematology 18 (2): 1. doi:10.1097/MOH.0b013e3283439964. PMID 21245760.

Wysham, NG; Allada G; Sullivan DR (2013). "An opportunistic infection associated with ruxolitinib, a novel janus kinase 1,2 inhibitor.". Chest 143 (5): 1478–9. doi:10.1378/chest.12-1604. PMID 23648912.

"FDA Approves Incyte's Jakafi(TM) (ruxolitinib) for Patients with Myelofibrosis" (Press release). Incyte.

http://www.ibtimes.co.uk/tofacitinib-citrate-arthritis-drug-that-cured-alopecia-universalis-1453489
International Business Times
June 20, 2014

Tofacitinib Citrate: The Arthritis Drug That Cured Alopecia Universalis

by

Hannah Osborne



An arthritis drug has been used to cure a man who was almost completely bald from alopecia universalis.

Tofacitinib citrate was used to treat the 25-year-old who had lost most of his hair after getting alopecia – a disease there is currently no long-term treatment or cure for.

The man had not grown hair for seven years. However, after being treated with the arthritis drug for just three months, he had regrown a head of hair, eyebrows, eyelashes, some facial hair and armpit hair.

Alopecia universalis occurs in approximately one in every 200,000 people. It is thought to be an auto immune disorder and can affect anyone at any age.

Senior author of the study Brett A King, a dermatologist from Yale University School of Medicine, said: "The results are exactly what we hoped for. This is a huge step forward in the treatment of patients with this condition.

"While it's one case, we anticipated the successful treatment of this man based on our current understanding of the disease and the drug. We believe the same results will be duplicated in other patients, and we plan to try."

As well as alopecia, the man was also diagnosed with plaque psoriasis, a condition that meant he had red scaly areas of skin.
alopecia
The patient's head a) before treatmen with tofacitinib, b) two months into treatment, c) five months into treatment, and d) eight months into treatment.Yale University

Researchers decided to try treating him with tofacitinib – an FDA approved drug for rheumatoid arthritis – as it had been successful used to treat psoriasis on humans in the past. It had also reversed alopecia areata, a less extreme form of the disease, in mice.

King thought the drug might address both diseases simultaneously. After two months of being treated with tofacitinib, the man's psoriasis had started to improve and he had started to grow hair. After three months, he had grown a full head of hair.

Study co-author Brittany G Craiglow said: "By eight months there was full regrowth of hair. The patient has reported feeling no side effects, and we've seen no lab test abnormalities, either."

Published in the Journal of Investigative Dermatology, the authors say this is the first reported case of a successful targeted treatment of alopecia universalis.

"There are no good options for long-term treatment of alopecia universalis," King said. "The best available science suggested this might work, and it has."

The drug treats alopecia by turning off the immune system's attack on hair follicles. The researchers have now submitted a proposal for a clinical trial of a cream form of tofacitinib for treatment of alopecia.



halfpasthuman.com

Clif High reports :

USA is #1!

World's first cFF (cyber false flag) invented here! And coming to a bank/gov't near you in September!

Linguistics show that USA politbureau is linking [banks] and [national security] very heavily. They will be shutting down banks in response to a [cyber false flag] and they will then use this as [excuse for war]. We all really know that this is to try and save some zionist bankster butts from a very early, and violent death later as the revolution heats up for a cold winter.

Their 'target' in this first ever cyber false flag is Russia.



http://www.naturalblaze.com/2014/08/can-this-new-solar-powered-device.html
August 16, 2014

Can This New Solar-Powered Device Purify Polluted Water?

by
Kevin Samson


Water shortages continue to make the news across the world, and governments seem to be offering very few if any solutions. Recently, I covered a novel low-cost, simple device called Warka Water that aims to extract water from the air and offer regions with little to no infrastructure the possibility of water self-sufficiency.

However, in addition to shortages, pollution is another grave problem; even if some areas technically have water it is often unfit to drink.

A sophomore in the Department of Civil, Structural and Environmental Engineering at the University of Buffalo, Deshawn Henry, believes he has found a solution.

Henry has created essentially a six-foot tall magnifying glass that he has termed a "water lens."

It is another low-cost solution that can reach areas that have little in the way of conventional infrastructure, offering a speedy way to self-sufficiency and decreased deaths from unsafe water.

Since the frame for the lens can be constructed from commonly found materials — wood, plastic sheeting and water — the lens can be built for almost no cost, offering an inexpensive method to treat water.

The device may not look like much, but it can heat a liter of water to between 130 and 150 degrees Fahrenheit in a little more than an hour, destroying 99.9 percent of bacteria and pathogens.

“The water lens could have a huge impact in developing countries,” says Henry ... “Millions of people die every year from diseases and pathogens found in unclean water, and they can’t help it because that’s all they have. Either they drink it or they die.”

Henry's device is still in the testing phase, but shows promise. The University of Buffalo relates the details that still need to be worked out in order to provide the most efficient, practical system that could be used on widespread basis by families.

The lens consists of a plastic sheet covered with water supported by a wooden frame. The frame holds a small container of water below the lens in line with a focal point created from a concentrated ray of sunlight. Barring the weather, once assembled, the lens functions freely. Due to the sun’s movement throughout the day, Henry needs to repeatedly shift the container to match the focal point.

Henry’s research tested how altering the thickness of the plastic sheet and the volume of water over the sheet affected the efficiency of the lens. The device was tested with plastic sheets that were 0.7, 1 and 2 millimeters thick, and water volumes of four, six and eight liters.

The study found that adding more water to the lens improved efficiency, as larger areas of water transmitted more energy from sunlight. However, thicker plastic sheets consumed more energy from light, lowering the lens’ efficiency.

A plastic sheet that was too thin or excessive amounts of water could break the lens. Henry concluded that the 0.7-millimeter sheet could efficiently heat the container while supporting eight liters of water, but any more and the sheet could potentially break.

With 1.1 billion people lacking access to clean drinking water, Henry’s work could make a difference in the world, says Jensen, who frequently mentors undergraduate students during summer research programs.

“I have seen how intense research activities can inspire UB students and educate the next generation of innovators,” says Jensen. “Deshawn’s work would allow a family in sunny regions to treat drinking water without having to expend energy or rely on imported technologies.”

Building a larger water lens that remains efficient is the next step in Henry’s research. A family of five would need a lens at least three times the size of the device he constructed, which was designed to heat one liter of water at a time, says Henry.

As fresh water continues to dwindle with recent studies showing that global crisis levels will be reached by 2040 and corporate water predators seek to hoard this "blue gold," Deshawn Henry's invention could be a welcome practical solution to maintaining water sovereignty.



http://www.buffalo.edu/ubreporter/featured-stories.host.html/content/shared/university/news/ub-reporter-articles/stories/2014/August/lens_purification.detail.html
August 14, 2014

Student’s water and solar-powered lens purifies polluted water

by
Marcene Robinson

“The water lens could have a huge impact in developing countries.”

Water may appear to be an abundant resource, but in some parts of the world clean water is hard to come by.

That could change through the work of Deshawn Henry, a sophomore civil engineering major, who researched how to improve a 6-foot-tall, self-sustaining magnifying glass.

Properly termed a water lens, the device uses another abundant resource — sunlight — to heat and disinfect polluted water. Since the frame for the lens can be constructed from commonly found materials — wood, plastic sheeting and water — the lens can be built for almost no cost, offering an inexpensive method to treat water.

The device may not look like much, but it can heat a liter of water to between 130 and 150 degrees Fahrenheit in a little more than an hour, destroying 99.9 percent of bacteria and pathogens.

“The water lens could have a huge impact in developing countries,” says Henry, who performed the study under James Jensen, professor in the Department of Civil, Structural and Environmental Engineering.

“Millions of people die every year from diseases and pathogens found in unclean water, and they can’t help it because that’s all they have. Either they drink it or they die.”

The lens consists of a plastic sheet covered with water supported by a wooden frame. The frame holds a small container of water below the lens in line with a focal point created from a concentrated ray of sunlight. Barring the weather, once assembled, the lens functions freely. Due to the sun’s movement throughout the day, Henry needs to repeatedly shift the container to match the focal point.

Henry’s research tested how altering the thickness of the plastic sheet and the volume of water over the sheet affected the efficiency of the lens. The device was tested with plastic sheets that were 0.7, 1 and 2 millimeters thick, and water volumes of four, six and eight liters.

The study found that adding more water to the lens improved efficiency, as larger areas of water transmitted more energy from sunlight. However, thicker plastic sheets consumed more energy from light, lowering the lens’ efficiency.

A plastic sheet that was too thin or excessive amounts of water could break the lens. Henry concluded that the 0.7-millimeter sheet could efficiently heat the container while supporting eight liters of water, but any more and the sheet could potentially break.

With 1.1 billion people lacking access to clean drinking water, Henry’s work could make a difference in the world, says Jensen, who frequently mentors undergraduate students during summer research programs.

Henry studied under Jensen through the UB Louis Stokes Alliance for Minority Participation (LSAMP) program, which connects underrepresented students with research opportunities in STEM fields. LSAMP is one of many programs in the Office of Undergraduate Education focused on increasing experiential-learning opportunities for students.

“I have seen how intense research activities can inspire UB students and educate the next generation of innovators,” says Jensen. “Deshawn’s work would allow a family in sunny regions to treat drinking water without having to expend energy or rely on imported technologies.”

Building a larger water lens that remains efficient is the next step in Henry’s research. A family of five would need a lens at least three times the size of the device he constructed, which was designed to heat one liter of water at a time, says Henry.



You've Got Male !

TSA Writes :
I Think I Love You ... Please Marry Me





Mexico's New Border-Tunneling Machine





JimStoneFreelance.com :


 

Islam Loves You !



Don't Lose Your Head Like These Ex-Hominids ! Keep It In Your Colon !

 

[ Don't Worry -- They're only Photoshopped Crisis-Actors ! ]

 



Don't Worry ! Jesus Will Save You -- AND Your Money ! AND the Dinosaurs !





Chump Change We Can Believe In !

Your Brain on ObamaCare :




 




Your Support Maintains this Service --

BUY


The Rex Research Civilization Kit

... It's Your Best Bet & Investment in Sustainable Humanity on Earth ...
Ensure & Enhance Your Survival & Genome Transmission ...

Everything @ rexresearch.com on a Data DVD !

ORDER PAGE