Melatonin -Bio-identical Hormone Therapy Anti-aging
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Production of melatonin by the pineal gland is inhibited by light and
permitted by darkness. For this reason melatonin has been called "the
hormone of darkness" and its onset each evening is called the Dim-Light
Melatonin Onset (DLMO). Secretion of melatonin as well as its level in
the blood, peaks in the middle of the night, and gradually falls during
the second half of the nigh.
Besides its function as synchronizer of the biological clock, melatonin
also exerts a powerful antioxidant activity. The discovery of melatonin
as an antioxidant was made in 1993.
Unlike other antioxidants, melatonin does not undergo redox cycling
Redox cycling may allow other antioxidants (such as vitamin C) to regain
their antioxidant properties. Melatonin, on the other hand, once
oxidized, cannot be reduced to its former state because it forms several
stable end-products upon reacting with free radicals. Therefore, it has
been referred to as a terminal (or suicidal) antioxidant.

Individuals with autism spectrum disorders (ASD) may have lower than
normal levels of melatonin. A 2008 study found that unaffected parents
of individuals with ASD also have lower melatonin levels, and that the
deficits were associated with low activity of the ASMT gene, which
encodes the last enzyme of melatonin synthesis.
Melatonin has been studied for the treatment of cancer, immune
disorders, cardiovascular diseases, depression, seasonal affective
disorder (SAD), circadian rhythm sleep disorders and sexual dysfunction.
Studies by Alfred J. Lewy at Oregon Health & Science University and
other researchers have found that it may ameliorate circadian
misalignment and SAD. Basic research indicates that melatonin may play a
significant role in modulating the effects of drugs of abuse such as
cocaine.
(Wikipedia) |