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Home arrow Research and Review arrow Testosterone Reduces NO Oxide Inhibiting Protein
Testosterone Reduces NO Oxide Inhibiting Protein PDF Print E-mail
Written by Robbie Durand   
Thursday, 10 April 2008
Asymmetric dimethylarginine (ADMA) is a naturally occurring component of human blood plasma. It is formed as a metabolic byproduct of continuous protein turnover in all cells of the body. More than one decade ago ADMA was first reported to exert biological effects by inhibiting NO synthesis. Many researchers today agree that ADMA may play a prominent role in the pathogenesis and in the progression of cardiovascular diseases - specifically atherosclerosis. There is an increasing body of epidemiological evidence that

links low testosterone levels with a profile of increased cardiovascular risks, the metabolic syndrome and type II diabetes in men. With regard to ADMA, prospective epidemiological data have shown that even slightly increased blood levels were associated with an increased risk of coronary events among

nonsmoking men. Testosterone has recently been showed to reduce the risk of cardiovascular disease yet the effects of testosterone on AMDA production are unknown. Men with low testosterone were enrolled in the study for 22 weeks. There was a significant decline in plasma ADMA values of approximately 10 % after 24 weeks of T administration of which 22 weeks. The reduction in AMDA is favorable on endothelial function since even slight changes in ADMA levels may impact cardiovascular risks in men.

 

Leifke E, Kinzel M, Tsikas D, Gooren L, Frölich JC, Brabant G. Effects of normalization of plasma
 testosterone levels in hypogonadal men on plasma levels and urinary excretion of asymmetric
 dimethylarginine (ADMA). Horm Metab Res. 2008 Jan;40(1):56-9

 
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