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・ Dehydration
・ Dehydration (disambiguation)
・ Dehydration reaction
・ Dehydrin
・ Dehydro-L-gulonate decarboxylase
・ Dehydroacetic acid
・ Dehydroalanine
・ Dehydroaltenusin
・ Dehydroamino acid
・ Dehydroascorbic acid
・ Dehydrocholic acid
・ Dehydrocorybulbine
・ Dehydrocurvularin
・ Dehydrodolichyl diphosphate synthase
・ Dehydroemetine
Dehydroepiandrosterone
・ Dehydroepiandrosterone sulfate
・ Dehydrogenase
・ Dehydrogenation
・ Dehydrogenation of amine-boranes
・ Dehydrogenative coupling of silanes
・ Dehydrogluconate dehydrogenase
・ Dehydrogluconokinase
・ Dehydrohalogenation
・ Dehydrohexahydroxydiphenic acid
・ Dehydronorketamine
・ Dehydroretinal
・ Dehydrosecodine
・ Dehyur
・ Dehzanun


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Dehydroepiandrosterone : ウィキペディア英語版
Dehydroepiandrosterone

Dehydroepiandrosterone/dehydroepiandrostenedione (DHEA, more correctly didehydroepiandrosterone), also known as androstenolone as well as 3β-hydroxyandrost-5-en-17-one or 5-androsten-3β-ol-17-one, is an important endogenous steroid hormone. In its pharmaceutical drug form it is called prasterone (INN). It is the most abundant circulating steroid hormone in humans,〔William F Ganong MD, 'Review of Medical Physiology', 22nd Ed, McGraw Hill, 2005, page 362.〕 in whom it is produced in the adrenal glands,〔''The Merck Index'', 13th Edition, 7798〕 the gonads, and the brain, where it functions predominantly as a metabolic intermediate in the biosynthesis of the androgen and estrogen sex steroids.〔 However, DHEA also has a variety of potential biological effects in its own right, binding to an array of nuclear and cell surface receptors, and acting as a neurosteroid.
==Medical aspects==
In women with adrenal insufficiency and the healthy elderly there is insufficient evidence to support the use of DHEA.

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