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<html>
<head><title>Gelatin, stress, longevity</title></head>
<body>
<h1>
Gelatin, stress, longevity
</h1>
<p>
<hr />
<hr />
</p>
<p>
<strong>The main bulk of an animal's body consists of water, protein, fat and bones. Fat tissue and bone are
metabolically more quiescent than the protein-water systems. During stress or starvation, or even
hibernation, animals lose lean mass faster than fat.</strong>
</p>
<p>
<strong>The amino acids that constitute protein have many hormone-like functions in their free state. When
our glucose (glycogen) stores have been depleted, we convert our own tissue into free amino acids, some
of which are used to produce new glucose. The amino acids cysteine and tryptophan, released in large
quantities during stress, have antimetabolic (thyroid-suppressing) and, eventually, toxic effects.
Hypothyroidism itself increases the catabolic turnover of protein, even though general metabolism is
slowed.</strong>
</p>
<p>
<strong>Other amino acids act as nerve-modifiers ("transmitters"), causing, for example, excitation or
inhibition.</strong>
</p>
<p>
<strong>Some of these amino acids, such as glycine, have a very broad range of cell-protective
actions.</strong>
</p>
<p>
<strong>Their physical properties, rather than their use for production of energy or other metabolic
function, are responsible for their important cytoprotective actions.</strong>
</p>
<p>
<strong>Gelatin (the cooked form of collagen) makes up about 50% of the protein in an animal, but a much
smaller percentage in the more active tissues, such as brain, muscle, and liver. 35% of the amino acids
in gelatin are glycine, 11% alanine, and 21% proline and hydroxyproline.</strong>
</p>
<p>
<strong>In the industrialized societies, the consumption of gelatin has decreased, relative to the foods
that contain an inappropriately high proportion of the antimetabolic amino acids, especially tryptophan
and cysteine.</strong>
</p>
<p>
<strong>The degenerative and inflammatory diseases can often be corrected by the use of gelatin-rich foods.
</strong>
</p>
<p>
<hr />
<hr />
</p>
<p>
I usually think about something for a long time before I get around to integrating it into my life,
sometimes because old habits have to be changed, but usually because our social organization is set up to do
things in conventional ways. Our foods reflect our social organization, enforced by laws and rules. When I
first went to Mexico to study, many traditional foods were still available even in the city--fried pig skin,
served crisp or boiled with a sauce, blood tacos, cartilaginous parts of various animals, chicken-foot soup,
crustaceans, insects, etc. Later, when I studied biochemistry, I realized that each part of an organism has
a characteristic chemistry and special nutritional value. I knew of Weston Price's research on traditional
diets, and his argument that the degenerative "diseases of civilization" were produced by the simplified
diets that are characteristic of the highly industrialized societies.
</p>
<p>
As I began to study endocrinology, I realized that there were some radical misconceptions behind the ideas
of "scientific nutrition." I. P. Pavlov, who had studied nutritional physiology because it constituted the
animal's closest interactions with its environment, was motivated by a desire to understand life in its
totality, including consciousness. But western nutritionists were nearly all committed to an ideology that
forced them to think in terms of "essential factors for growth," leading to ideas such as "minimum daily
requirement" for each nutrient. Bodily bulk (especially body length) was the criterion, not the experienced
quality of life. And there has been no scarcity of evidence showing that rapid bodily growth has its
drawbacks (e.g., Miller, et al., 2002, "Big mice die young").
</p>
<p>
One of the brightest of the genetically oriented nutritionists, Roger Williams, used the idea of genetic
individuality to explain that the popular idea of a species-wide standard diet couldn't be applied to
exceptional individuals, and that disease was often the result of the mismatch between special nutritional
requirements and a "standard" diet. Linus Pauling's concept of orthomolecular medicine was a restatement of
Williams' principle for the general scientific community.
</p>
<p>
But still, the emphasis was on the match between a specific chemical and the <strong><em>genetic
constitution</em></strong> of the organism. Pavlov's idea of the "trophic" actions of nerves was
discarded, and the rest of his work was relegated to a crudely caricatured branch of psychology. His
therapeutic recommendation of beef broth for many ailments was ignored as having nothing to do with the
caricatured "Pavlovism."
</p>
<p>
If nerves are intimately involved in the processes of nutrition and development, the effects of nutrients on
the nerves and their development should have a central place in nutritional research. Our appetites reflect
our biochemical needs, and our "unconditional reflexes" are likely to be wiser than the theories that are
based simply on the amount of weight a young animal gains on a particular diet.
</p>
<p>
When I began teaching endocrinology, some of my students didn't want to hear about anything except "lock and
key" endocrinology, in which "a hormone" signals certain cells that have a suitable receptor for that
hormone. But the studies of Hans Selye and Albert Szent-Gyorgyi made it clear that Pavlov's global, holistic
approach to the organism in its environment was the soundest scientific basis for physiology, including
endocrinology. A cell's response to a hormone depended on the state of the cell. Nutrients and metabolites
and hormones and neurotransmitters all modify the cell's sensitivity to its surroundings. The assumptions of
"molecular biology," as generally understood, are fundamentally mistaken.
</p>
<p>
The idea of fixed requirements for specific nutrients, and especially the idea that rapid physical growth
was the way to determine the essentiality of a substance, led to a monstrous distortion of the official
dietary recommendations. Business, industry, government, and the health professions collaborated in the
propagation of an ideology about nutrition that misrepresented the nature of the living organism.
</p>
<p>
Most studies of the nutritional requirements for protein have been done for the agricultural industries, and
so have been designed to find the cheapest way to get the maximum growth in the shortest time. The industry
isn't interested in the longevity, intelligence, or happiness of their pigs, chickens, and lambs. The
industry has used chemical growth stimulants in combination with the foods that support rapid growth at
least expense. Antibiotics and arsenic and polyunsaturated fatty acids have become part of our national food
supply because they produce rapid weight gain in young animals.
</p>
<p>
The amino acids in proteins have been defined as "essential" on the basis of their contribution to growth,
ignoring their role in producing long life, good brain development, and good health. The amino acid and
protein requirements during aging have hardly been studied, except in rats, whose short life-span makes such
studies fairly easy. The few studies that have been done indicate that the requirements for tryptophan and
cysteine become very low in adulthood.
</p>
<p>
Although Clive McKay's studies of life extension through caloric restriction were done in the 1930s, only a
few studies have been done to find out which nutrients' restriction contributes most to extending the life
span. Restricting toxic heavy metals, without restricting calories, produces about the same life-extending
effect as caloric restriction. <strong>
Restricting only tryptophan, or only cysteine, produces a greater extension of the life span than
achieved in most of the studies of caloric restriction.</strong>
How great would be the life-span extension if both tryptophan and cysteine were restricted at the same time?
</p>
<p>
Both tryptophan and cysteine inhibit thyroid function and mitochondrial energy production, and have other
effects that decrease the ability to withstand stress. Tryptophan is the precursor to serotonin, which
causes inflammation, immunodepression, and generally the same changes seen in aging. Histidine is another
amino acid precursor to a mediator of inflammation, histamine<strong>; </strong>
would the restriction of histidine in the diet have a longevity promoting effect, too?
</p>
<p>
It happens that gelatin is a protein which contains no tryptophan, and only small amounts of cysteine,
methionine, and histidine. Using gelatin as a major dietary protein is an easy way to restrict the amino
acids that are associated with many of the problems of aging.
</p>
<p>
The main amino acids in gelatin are glycine and proline<strong>; </strong>
alanine is also present in significant quantity. Glycine and proline are responsible for the unusual fibrous
property of collagen.
</p>
<p>
An animal's body, apart from fat and water, is mostly protein, and about half of the protein in the body is
collagen (which is the native, uncooked form of gelatin). Its name is derived from its traditional use as
glue. It is responsible for the structural toughness of mature animal bodies.
</p>
<p>
When cells are stressed, they form extra collagen, but they can also dissolve it, to allow for tissue
remodeling and growth. Invasive cancers over-produce this kind of enzyme, destroying the extracellular
matrix which is needed for normal cellular differentiation and function. When collagen is broken down, it
releases factors that promote wound healing and suppress tumor invasiveness. (Pasco, et al., 2003) Glycine
itself is one of the factors promoting wound healing and tumor inhibition.
</p>
<p>
It has a wide range of antitumor actions, including the inhibition of new blood vessel formation
(angiogenesis), and it has shown protective activity in liver cancer and melanoma. Since glycine is
non-toxic (if the kidneys are working, since any amino acid will contribute to the production of ammonia),
this kind of chemotherapy can be pleasant.
</p>
<p>
When we eat animal proteins in the traditional ways (for example, eating fish head soup, as well as the
muscles, or "head-cheese" as well as pork chops, and chicken-foot soup as well as drumsticks), we assimilate
a large amount of glycine and gelatin. This whole-animal balance of amino acids supports all sorts of
biological process, including a balanced growth of children's tissues and organs.
</p>
<p>
When only the muscle meats are eaten, the amino acid balance entering our blood stream is the same as that
produced by extreme stress, when cortisol excess causes our muscles to be broken down to provide energy and
material for repair. The formation of serotonin is increased by the excess tryptophan in muscle, and
serotonin stimulates the formation of more cortisol, while the tryptophan itself, along with the excess
muscle-derived cysteine, suppresses the thyroid function.
</p>
<p>
A generous supply of glycine/gelatin, against a balanced background of amino acids, has a great variety of
antistress actions. Glycine is recognized as an "inhibitory" neurotransmitter, and promotes natural sleep.
Used as a supplement, it has helped to promote recovery from strokes and seizures, and to improve learning
and memory. But in every type of cell, it apparently has the same kind of quieting, protective antistress
action. The range of injuries produced by an excess of tryptophan and serotonin seems to be prevented or
corrected by a generous supply of glycine. Fibrosis, free radical damage, inflammation, cell death from ATP
depletion or calcium overload, mitochondrial damage, diabetes, etc., can be prevented or alleviated by
glycine.
</p>
<p>
Some types of cell damage are prevented almost as well by alanine and proline as by glycine, so the use of
gelatin, rather than glycine, is preferable, especially when the gelatin is associated with its normal
biochemicals. For example, skin is a rich source of steroid hormones, and cartilage contains "Mead acid,"
which is itself antiinflammatory.
</p>
<p>
The other well-studied inhibitory neurotransmitter is GABA, so it's significant that GABA (gamma amino
butyric acid) is a close analog of glycine (alpha amino acetic acid). A synthetic molecule structurally
similar to those natural inhibitory "transmitters," beta amino propanoic acid, has some of the protective
effects of glycine and GABA. The other molecules in the series, at least up to epsilon amino caproic acid,
have some of the same antiinvasive, antiinflammatory, anti-angiogenic, properties. Alanine and proline, with
cell-protecting actions, have the same basic composition, carbon (CH2 or CH) atoms separating acid and amino
groups. Even the amino acids in which the lipophilic carbon atoms extend out in a branched side-chain,
valine, leucine, and isoleucine, have some of the antiseizure (inhibitory) action (Skeie, et al., 1992,
1994) of GABA and glycine. Tests done with one, or a few, of the relatively lipophilic (aliphatic) amino
acids prevent seizures, while the "balanced" mixtures of amino acids permit seizures<strong>;</strong>
unfortunately, results of this sort haven't led researchers to question the idea of "balance" that developed
within the setting of agricultural research.
</p>
<p>
The similarity between the structures and actions of glycine and GABA suggest that their "receptors" are
similar, if not identical. For years, it has been known that progesterone and pregnenolone act on the GABA
receptor, to reinforce the protective, inhibitory effects of GABA. Estrogen has the opposite effect,
inhibiting GABA's action. Since GABA opposes estrogen and inhibits the growth of breast cancer, it wouldn't
be surprising if glycine, alanine, etc., did the same.
</p>
<p>
Recent research shows that progesterone and its metabolites also act on the "glycine receptor," increasing
inhibition, and that the "phytoestrogen," genistein, antagonizes the inhibitory effect of glycine.
</p>
<p>
The inhibitory systems are opposed by excitatory systems, especially by the excitatory amino acid system,
activated by glutamic and aspartic acid. Progesterone and estrogen act on that system, too, decreasing and
increasing excitation, respectively.
</p>
<p>
I have previously discussed the arguments for viewing progesterone as a "cardinal adsorbent" (as in Ling and
Fu, 1987, 1988, Ling, et al., 1984, a steroid alters glycine's influence on the cell's electrical behavior)
which increases the lipophilic, fat-loving property of the cytoplasm, and estrogen as having the opposite
action, increasing the water-loving hydrophilic quality of the cytoplasm. If we think of the proteins known
as the GABA and glycine receptors as having some regions in which the basic amine of lysine associates with
the acidic group of aspartic or glutamic acid, then the action of glycine, or other amino acids would be to
introduce additional lipophilic carbon atoms into those regions (with the amino acids' polar ends pairing
with their opposites on the protein), where the cardinal adsorbents exert their influence.
</p>
<p>
Generally, biologists seem puzzled by such facts, because they don't fit into the "lock and key" model of
molecular biology. But I think they make the organism easier to understand, since these constellations of
facts illustrate simple and general physical principles. They suggest the idea that estrogen and
progesterone and glycine, GABA, etc., will be active in any functioning cell, at a suitable concentration.
It was this kind of thinking in terms of general physical principles that led Szent-Gyorgyi to investigate
the effects of estrogen and progesterone on heart physiology. The old characterization of estrogen and
progesterone as "sex" and "pregnancy" hormones acting on a few tissues through specific receptors never had
a good basis in evidence, but the accumulated evidence has now made those ideas impossible for an informed
person to accept. (Progesterone increases the heart's pumping efficiency, and estrogen is antagonistic, and
can produce cardiac arrhythmia.)
</p>
<p>
In the context of the excitatory actions of estrogen, and the inhibitory action of glycine, it would be
reasonable to think of glycine as one of the antiestrogenic substances. Another type of amino acid, taurine,
is structurally similar to glycine (and to beta amino propanoic acid, and to GABA), and it can be thought of
as antiestrogenic in this context. The specific kinds of excitation produced by estrogen that relate to
reproduction occur against a background of very generalized cellular excitation, that includes increased
sensitivity of sensory nerves, increased activity of motor nerves, changes in the EEG, and, if the estrogen
effect is very high, epilepsy, tetany, or psychosis.
</p>
<p>
Glycine's inhibitory effects appear to oppose estrogen's actions generally, in sensory and motor nerves, in
regulating angiogenesis, and in modulating the cytokines and "chemokines" that are involved in so many
inflammatory and degenerative diseases, especially tumor necrosis factor (TNF), nitric oxide (NO), and
prostaglandins. Exposure to estrogen early in life can affect the health in adulthood, and so can an early
deficiency of glycine. The degenerative diseases can begin in the earliest years of life, but because aging,
like growth, is a developmental process, it's never too late to start the corrective process.
</p>
<p>
One of estrogen's "excitatory" effects is to cause lipolysis, the release of fatty acids from storage
fat<strong>; </strong>
it directs the conversion of glucose into fat in the liver, so that the free fatty acids in the circulation
remain chronically high under its influence. The free fatty acids inhibit the oxidation of glucose for
energy, creating insulin resistance, the condition that normally increases with aging, and that can lead to
hyperglycemia and "diabetes."
</p>
<p>
Gelatin and glycine have recently been reported to facilitate the action of insulin in lowering blood sugar
and alleviating diabetes. Gelatin has been used successfully to treat diabetes for over 100 years (A.
Guerard, Ann Hygiene 36, 5, 1871; H. Brat, Deut. Med. Wochenschrift 28 (No. 2), 21, 1902). Glycine inhibits
lipolysis (another antiexcitatory, "antiestrogenic" effect), and this in itself will make insulin more
effective, and help to prevent hyperglycemia. (A gelatin-rich diet can also lower the serum triglycerides.)
Since persistent lipolysis and insulin resistance, along with a generalized inflammatory state, are involved
in a great variety of diseases, especially in the degenerative diseases, it's reasonable to consider using
glycine/gelatin for almost any chronic problem. (Chicken foot soup has been used in several cultures for a
variety of ailments; chicken foot powder has been advocated as a stimulant for spinal cord
regeneration--Harry Robertson's method was stopped by the FDA).
</p>
<p>
Although Hans Selye observed as early as the 1930s that stress causes internal bleeding (in lungs, adrenals,
thymus, intestine, salivary and tear glands, etc.), the medical establishment, which has the opportunity to
see it after surgery, burns or other trauma, and following strokes and head injuries, prefers to explain it
by "stomach hyperacidity," as if it were limited to the stomach and duodenum. And the spontaneous bruising,
and easy bruising, that is experienced by millions of women, especially with the premenstrual syndrome, and
nose bleeds, and scleral bleeding, purpura senilis, urinary bleeding, bleeding gums, and many other kinds of
"spontaneous" or stress related bleeding, are treated by main-line medicine as if they had no particular
physiological significance.
</p>
<p>
Stress is an energy problem, that leads to the series of hormonal and metabolic reactions that I have often
written about--lipolysis, glycolysis, increased serotonin, cortisol, estrogen, prolactin, leaky capillaries,
protein catabolism, etc. The capillaries are among the first tissues to be damaged by stress.
</p>
<p>
Although Selye showed that estrogen treatment mimics shock and stress, and that progesterone prevents the
stress reaction, the effects of these hormones on the circulatory system have never been treated
systematically. Katherina Dalton observed that progesterone treatment prevented the spontaneous bruising of
the premenstrual syndrome<strong>;</strong> Soderwall observed that estrogen caused enlargement of the
adrenals, sometimes with hemorrhage and necrosis<strong>;</strong> old female animals often have bleeding in
the adrenals (Dhom, et al., 1981). Strangely, estrogen's induction of uterine bleeding has been
compartmentalized, as if the endometrial blood vessels didn't follow the same rules as vessels elsewhere in
the body. Both estrogen and cortisol are known to cause clotting disorders and to increase capillary
fragility, but these steroids have been elevated to the realm of billion dollar drug products, beyond the
reach of ordinary physiological thinking. Other stress-released substances that are entangled in the drug
market (tryptophan, serotonin, nitric oxide, and unsaturated fats, for example) are similarly exempt from
consideration as factors in circulatory, neoplastic, and degenerative diseases.
</p>
<p>
At the time Selye was observing stress-induced bleeding, standard medicine was putting gelatin to
use--orally, subcutaneously, and intravenously--to control bleeding. Since ancient times, it had been used
to stop bleeding by applying it to wounds, and this had finally been incorporated into medical practice.
</p>
<p>
The 1936 Cyclopedia of Medicine (G.M. Piersol, editor, volume 6) mentions the use of gelatin solution to
quickly control nosebleeds, excessive menstrual bleeding, bleeding ulcers (using three doses of 18 grams as
a 10% solution during one day), and bleeding from hemorrhoids and the lower bowel, and hemorrhage from the
bladder. But since Selye's work relating the thrombohemorrhagic syndromes to stress wasn't known at that
time, gelatin was thought of as a useful drug, rather than as having potentially far-reaching physiological
effects, antagonizing some of the agents of stress-induced tissue damage.
</p>
<p>
Skin cells and nerve cells and many other cells are "electrically" stabilized by glycine, and this effect is
currently being described in terms of a "chloride current." A variety of mechanisms have been proposed for
the protective effects of some of the amino acids, based on their use as energy or for other metabolic
purpose, but there is evidence that glycine and alanine act protectively without being metabolized, simply
by their physical properties.
</p>
<p>
A small dose of glycine taken shortly after suffering a stroke was found to accelerate recovery, preventing
the spreading of injury through its inhibitory and antiinflammatory actions. Its nerve-stabilizing action,
increasing the amount of stimulation required to activate nerves, is protective in epilepsy, too. This
effect is important in the regulation of sleep, breathing, and heart rhythm.
</p>
<p>
Glycine's antispastic activity has been used to alleviate the muscle spasms of multiple sclerosis. It is
thought to moderate some of the symptoms of schizophrenia.
</p>
<p>
A recent publication shows that glycine alleviates colitis; but the use of gelatin, especially in the form
of a concentrated gelatinous beef broth, for colitis, dysentery, ulcers, celiac disease, and other diseases
of the digestive system, goes far back in medical history. Pavlov's observation of its effectiveness in
stimulating the secretion of digestive juices occurred because the stimulating value of broth was already
recognized.
</p>
<p>
Although I pointed out a long time ago the antithyroid effects of excessive cysteine and tryptophan from
eating only the muscle meats, and have been recommending gelatinous broth at bedtime to stop nocturnal
stress, it took me many years to begin to experiment with large amounts of gelatin in my diet. Focusing on
the various toxic effects of tryptophan and cysteine, I decided that using commercial gelatin, instead of
broth, would be helpful for the experiment. For years I hadn't slept through a whole night without waking,
and I was in the habit of having some juice or a little thyroid to help me go back to sleep. The first time
I had several grams of gelatin just before bedtime, I slept without interruption for about 9 hours. I
mentioned this effect to some friends, and later they told me that friends and relatives of theirs had
recovered from long-standing pain problems (arthritic and rheumatic and possibly neurological) in just a few
days after taking 10 or 15 grams of gelatin each day.
</p>
<p>
For a long time, gelatin's therapeutic effect in arthritis was assumed to result from its use in repairing
the cartilage or other connective tissues around joints, simply because those tissues contain so much
collagen. (Marketers suggest that eating cartilage or gelatin will build cartilage or other collagenous
tissue.) Some of the consumed gelatin does get incorporated into the joint cartilage, but that is a slow
process, and the relief of pain and inflammation is likely to be almost immediate, resembling the
antiinflammatory effect of cortisol or aspirin.
</p>
<p>
Inflammation produces fibrosis, because stress, hypoxia, and inadequate supply of glucose stimulate the
fibroblasts to produce increased amounts of collagen. In lungs, kidneys, liver, and other tissues, glycine
protects against fibrosis, the opposite of what the traditional view would suggest.
</p>
<p>
Since excess tryptophan is known to produce muscle pain, myositis, even muscular dystrophy, gelatin is an
appropriate food for helping to correct those problems, simply because of its lack of tryptophan. (Again,
the popular nutritional idea of amino acids as simply building blocks for tissues is exactly wrong--muscle
protein can exacerbate muscle disease.) All of the conditions involving excess prolactin, serotonin, and
cortisol (autism, postpartum and premenstrual problems, Cushing's disease, "diabetes," impotence, etc.)
should benefit from reduced consumption of tryptophan. But the specifically antiinflammatory amino acids in
gelatin also antagonize the excitatory effects of the tryptophan-serotonin-estrogen- prolactin system.
</p>
<p>
In some of the older studies, therapeutic results improved when the daily gelatin was increased. Since 30
grams of glycine was commonly used for treating muscular dystrophy and myasthenia gravis, a daily intake of
100 grams of gelatin wouldn't seem unreasonable, and some people find that quantities in that range help to
decrease fatigue. For a growing child, though, such a large amount of refined gelatin would tend to displace
other important foods. The National Academy of Sciences recently reviewed the requirements for working
adults (male and female soldiers, in particular), and suggested that 100 grams of balanced protein was
needed for efficient work. For adults, a large part of that could be in the form of gelatin.
</p>
<p>
If a person eats a large serving of meat, it's probably helpful to have 5 or 10 grams of gelatin at
approximately the same time, so that the amino acids enter the blood stream in balance.
</p>
<p>
Asian grocery stores are likely to sell some of the traditional gelatin-rich foods, such as prepared pig
skin and ears and tails, and chicken feet.
</p>
<p>
Although the prepared powdered gelatin doesn't require any cooking, dissolving it in hot water makes it
digest a little more quickly. It can be incorporated into custards, mousses, ice cream, soups, sauces,
cheese cake, pies, etc., or mixed with fruit juices to make desserts or (with juice concentrate) candies.
</p>
<p>
Although pure glycine has its place as a useful and remarkably safe drug, it shouldn't be thought of as a
food, because manufactured products are always likely to contain peculiar contaminants.
</p>
<p><strong> </strong></p>
<p>
<strong><h3>REFERENCES</h3></strong>
</p>
<p>
Am J Physiol. 1990 Jul;259(1 Pt 2):F80-7. <strong>Mechanisms of perfused kidney cytoprotection by alanine
and glycine.</strong> Baines AD, Shaikh N, Ho P.
</p>
<p>
Neurol. 1974; 24:392. <strong>Preliminary study of glycine administration in patients with
spasticity.</strong> Barbeau A.
</p>
<p>
Virchows Arch B Cell Pathol Incl Mol Pathol. 1981;36(2-3):195-206. <strong>Peliosis of the female adrenal
cortex of the aging rat.</strong> Dhom G, Hohbach C, Mausle E, Scherr O, Uebergerg H. Foci of apparent
peliosis are regularly observed in the mid-zone of the adrenal cortex in female rats older than 600 days.
The changes present range from ectasis of the sinusoids to extensive cystic change of the whole organ.
<strong>This lesion occurs almost exclusively in female animals and was seen in only one of 50 male animals
older than 600 days examined.</strong> Experimental stimulation or inhibition did not influence adrenal
peliosis. Electron microscopically, there was marked pericapillary edema with collapse of the capillaries,
and erythrocytes and thrombocytes were seen infiltrating the edema. Fibrin accumulated in the larger foci.
Degenerative alterations were not observed either in the epithelial cells of the cortex or in mesenchymal
cells. The pathogenesis is unknown, but the possible role of <strong>constant estrus in aging female rats
will be discussed.</strong>
</p>
<p>
Riv Neurol. 1976 Mar-Jun;46(3):254-61.<strong>
[Antagonism between focal epilepsy and taurine administered by cortical Perfusion]</strong> Durelli L,
Quattrocolo G, Buffa C, Valentini C, Mutani R. The therapeutic action of taurine cortical perfusion was
tested in cats affected with Premarin and cobalt cortical epileptogenic foci. In all animals taurine
provoked the disappearance of EEG epileptic abnormalities. In the case of Premarin focus the effect appeared
more quickly than in the cobalt one. This different time-course, according to previous reports on the
antiepileptic action of the parenteral administration of the amino acid, <strong>suggests the hypothesis of
a taurine direct inhibitory action against Premarin focus</strong> and, on the contrary, a mediated
action towards the cobalt's. The latter might be related to the metabolic production of some taurine
derivative.
</p>
<p>
Ann Neurol. 1998; 44:261-265. <strong>Beneficial effects of L-serine and glycine in the management of
seizures in 3-phosphoglycerate dehydrogenase deficiency.</strong> de Kooning JT, Duran M, Dorling L, et
al.
</p>
<p>
Arch Gen Psychiatry. 1999; 56:29-36.<strong>
Efficacy of high-dose glycine in the treatment of enduring negative symptoms of schizophrenia.</strong>
Heresco-Levy U, Javitt DC, Ermilov M, et al.
</p>
<p>
Free Radic Biol Med. 2001 Nov 15;31(10):1236-44. <strong>Dietary glycine inhibits activation of nuclear
factor kappa B and prevents liver injury in hemorrhagic shock in the rat.</strong> Mauriz JL, Matilla B,
Culebras JM, Gonzalez P, Gonzalez-Gallego J. "Feeding the rats glycine significantly reduced mortality, the
elevation of plasma<strong> </strong>
transaminase levels and hepatic necrosis. <strong>The increase in plasma TNFalpha and nitric oxide (NO) was
also blunted by glycine feeding."</strong>
</p>
<p>
Am Fam Phys 1979 May;19(5):77-86. <strong>
'Not Cushing's syndrome'.</strong> Rincon J, Greenblatt RB, Schwartz RP Cushing's syndrome is
characterized by protein wasting secondary to hypergluconeogenesis, which produces thin skin, poor muscle
tone, osteoporosis and <strong>capillary fragility.</strong> These features distinguish patients with true
Cushing's syndrome from those who have some of the clinical findings often associated with the syndrome,
such as obesity, hypertension, striae and hirsutism. The dexamethasone suppression test helps identify
patients with pseudo-Cushing's syndrome.
</p>
<p>
Carcinogenesis. 1999; 20:2075-2081. <strong>Dietary glycine prevents the development of liver tumors caused
by the peroxisome proliferator WY-14, 643</strong>. Rose ML, Cattley RC, Dunn C, et al.
</p>
<p>
Carcinogenesis, Vol. 20, No. 5, 793-798, May 1999.<strong>
Dietary glycine inhibits the growth of B16 melanoma tumors in mice.</strong>
<hr />
</p>
<p>
Carcinogenesis, Vol. 20, No. 11, 2075-2081, November 1999. <strong>Dietary glycine prevents the development
of liver tumors caused by the peroxisome proliferator WY-14,643.</strong> M.L.Rose, R.C.Cattley1,
C.Dunn, V.Wong, Xiang Li and R.G.Thurman. Simpson RK Jr, Gondo M, Robertson CS, Goodman JC. <strong>The
influence of glycine and related compounds on spinal cord injury-related spasticity.</strong>
Neurochem Res. 1995; 20:1203-1210.
</p>
<p>
Neurochem Res. 1995 Oct;20(10):1203-10. <strong>
The influence of glycine and related compounds on spinal cord injury-induced spasticity.</strong>
Simpson RK Jr, Gondo M, Robertson CS, Goodman JC.
</p>
<p>
Neurochem Res. 1996 Oct;21(10):1221-6. <strong>Reduction in the mechanonociceptive response by intrathecal
administration of glycine and related compounds.</strong>
Simpson RK Jr, Gondo M, Robertson CS, Goodman JC.
</p>
<p>
Neurol Res. 1998 Mar;20(2):161-8. <strong>Glycine receptor reduction within segmental gray matter in a rat
model in neuropathic pain.</strong> Simpson RK Jr, Huang W.
</p>
<p>
Neurol Res. 2000 Mar;22(2):160-4. <strong>Long-term intrathecal administration of glycine prevents
mechanical hyperalgesia in a rat model of neuropathic pain.
</strong>Huang W, Simpson RK.
</p>
<p>
Pharmacol Biochem Behav. 1992 Nov;43(3):669-71. <strong>Branched-chain amino acids increase the seizure
threshold to picrotoxin in rats.</strong> Skeie B, Petersen AJ, Manner T, Askanazi J, Jellum E, Steen
PA.
</p>
<p>
Thromb Diath Haemorrh Suppl 1968;30:165-9<strong> [Purpura of the premenstrum and climacteric]. </strong>
[Article in German]<strong> </strong>Stamm H.
</p>
<p>
Toth E, Lajtha A. <strong>Glycine potentiates the action of some anticonvulsant drugs in some seizure
models.</strong> Neurochem Res. 1984; 9:1711-1718.
</p>
<p>
Sheng Li Ke Xue Jin Zhan. 2000 Jul;31(3):231-3. <strong>
[The roles of estrogen and progestin in epileptogenesis and their mechanisms of action]</strong>
[Article in Chinese] Wang Q.
</p>
<p>
FASEB J. 2000; 14:476-484.<strong>
Glycine-gated channels in neutrophils attenuate calcium influx and superoxide production.</strong>
Wheeler M, Stachlewitz RT, Yamashina S, et al.
</p>
<p>
Cell Mol Life Sci.1999; 56:843-856. <strong>Glycine: a new anti-inflammatory immunonutrient.</strong>
Wheeler MD, Ikejema K, Mol Life Sci. Enomoto N, et al.
</p>
<p>
Nutr Cancer. 2001;40(2):197-204. <strong>Endothelial cells contain a glycine-gated chloride channel.</strong
> Yamashina S, Konno A, Wheeler MD, Rusyn I, Rusyn EV, Cox AD, Thurman RG. "<strong>Glycine inhibited growth
of B16 melanoma tumors in vivo most likely because of the inhibition of angiogenesis. Here, the
hypothesis that the anticancer effect of glycine in vivo is due to expression of a glycine-gated Cl-
channel in endothelial cells was tested.</strong>
</p>
<p>
Biull Eksp Biol Med. 1981 Nov;92(11):599-601. <strong>[Repair processes in wound tissues of experimental
animals following administration of glycine]
</strong>
[Article in Russian] Zaidenberg MA, Pisarzhevskii SA, Nosova IM, Kerova AN, Dudnikova GN. A study was made
of the effect of glycine given in doses approximating the physiological ones on the repair of processes in
rat wound tissues. It was disclosed that in the early periods of wound healing, glycine administration leads
to the increased content of cAMP and cAMP/cGMP ratio in the wound muscle and then in the granulation tissue,
which appears to promote the intensification of the repair processes manifesting in the changes in tissue
metabolism (DNA, collagen), in anti-inflammatory action, as well as in a more rapid maturation of the
granulation tissue and wound reduction.. It was also found that the doses of glycine tested do not affect
the content of insulin and hydrocortisone in the blood of experimental animals.
</p>
<p>
<strong>"In recent years, evidence has mounted in favor of the antiinflammatory, immunomodulatory and
cytoprotective effects of the simplest amino acid L-glycine." "Glycine protects against shock caused by
hemorrhage, endotoxin and sepsis, prevents ischemia/reperfusion and cold storage/reperfusion injury to a
variety of tissues and organs including liver, kidney, heart, intestine and skeletal muscle, and
diminishes liver and renal injury caused by hepatic and renal toxicants and drugs. Glycine also protects
against peptidoglycan polysaccharide-induced arthritis..." and inhibits gastric secretion "....and
protects the gastric mucosa against chemically and stress-induced ulcers. Glycine appears to exert
several protective effects, including antiinflammatory, immunomodulatory and direct cytoprotective
actions. Glycine acts on inflammatory cells such as macrophages to suppress activation of transcription
factors and the formation of free radicals and inflammatory cytokines. In the plasma membrane, glycine
appears to activate a chloride channel that stabilizes or hyperpolarizes the plasma membrane potential.
As a consequence, .... opening of ... calcium channels and the resulting increases in intracellular
calcium ions are suppressed, which may account for the immunomodulatory and antiinflammatory effects of
glycine. Lastly, glycine blocks the opening of relatively non-specific pores in the plasma membrane that
occurs as the penultimate event leading to necrotic cell death."
</strong>
</p>
<p>
<strong> </strong>
Zhong Z, Wheeler MD, Li X, Froh M, Schemmer P, Yin M, Bunzendaul H, Bradford B, Lemasters JJ.<strong>,
</strong>"L-Glycine: a novel antiinflammatory, immunomodulatory, and cytoprotective agent." Curr Opin Clin
Nutr Metab Care. 2003 Mar;6(2):229-40. © Ray Peat Ph.D. 2009. All Rights Reserved. www.RayPeat.com
</p>
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