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Glycine
Sources
of glycine
High protein food contains good amounts of glycine and
is present in fish, meat, beans, and dairy products.
Benefits of glycine
It is required to build protein in the body and synthesis
of nucleic acids, the construction of RNA as well as DNA,
bile acids and other amino acids in the body. It is further
found to be useful in aiding the absorption of calcium in
the body.
It helps in retarding degeneration of muscles since it helps
to supply extra creatine in the body. Glycine has been found
to be helpful in the treatment of low pituitary gland function
and, because it supplies the body with additional creatine,
it has also been found effective in the treatment of progressive
muscular dystrophy.
It is also used for the treatment of hypoglycemia. Glycine
stimulates the release of glucagon, which mobilizes glycogen,
which is then released into the blood as glucose.
It is also found in fairly large amounts in the prostate fluid
and may for this reason be important in prostate health.
The glycine amino acid is also used by the nervous system
and its function as an inhibitory neurotransmitter makes it
important to help prevent epileptic seizures and it is also
used in the treatment of manic depression and hyperactivity.
Glycine supplies additional creatine to muscles and is used
to construct DNA and RNA. It functions in skin, connective
tissues, the central nervous system and prostrate.
A proper level of cellular glycine produces more energy, but
too much glycine can cause fatigue.
Deficiency symptoms of glycine
Few people are glycine deficient, in part because the body
makes its own supply of the non-essential amino acids, and
because it is abundant in food sources.
Symptoms of high intake
No clear toxicity has emerged from glycine studies, however
individuals with kidney or liver disease should not consume
high intakes of amino acids without consulting a medical physician.
When more in needed
In a study where men were given extra glycine over a period
of time, it reduced the symptoms of prostatic hyperplasia.
Daily requirement
The daily requirement is given in the recommended daily
allowance but be aware that this dosage is the minimum that
you require per day, to ward off serious deficiency of this
particular nutrient. In the therapeutic use of this nutrient,
the dosage is usually increased considerably, but the toxicity
level must be kept in mind.
Some
other points
Primary hyperoxaluria is a metabolic disease in which excess
oxalic acid is excreted in the urine. The excess oxalate is
of endogenous origin due to deficiency of alanine. Transaminase
together with some impairment of oxidation of glyoxylate to
formate may be the biochemical explanation foe the inherited
metabolic disease- the primary hyperoxaluria. In vitamin B6
deficiency, excess oxalate is excreted in the urine if excess
glycine is fed.
Glycine in conjugation with benzoyl CoA, forms the hippuric
acid. In the presence of cholic acid, it also forms the bile
acid known as glycholic acid.
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