抗雄激素。

Advances in sex hormone research Pub Date : 1976-01-01
R O Neri
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引用次数: 0

摘要

许多抗雄激素,主要是甾体和一些非甾体药物,已经合成并在几种可用的生物分析中进行了测试。不幸的是,许多这些化合物具有其他生物活性,这使得很难确定抗雄激素作用的确切机制。雄激素作用的阻断可以通过以下几种方式实现:(1)抑制促性腺激素的释放和/或合成,(2)干扰睾酮和/或双氢睾酮的生物合成,(3)阻断蛋白质合成,(4)在受体位点与雄激素竞争。虽然开发抗雄激素的主要原因是为了在某些临床情况下利用它们,但一些抗雄激素已成为研究雄激素作用的重要工具,特别是在分子水平上。一些抗雄激素治疗前列腺增生、多毛症和痤疮的临床疗效代表了治疗学的重要进展,但寻找副作用最小的更有效的抗雄激素应继续进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiandrogens.

Many antiandrogens, mainly steroidal and some nonsteroidal agents, have been synthesized and tested in several available biological assays. Unfortunately, many of these compounds have other biological activities which make it difficult to ascertain the precise mechanism of antiandrogenic action. The blocking of androgen action can be accomplished by a number of ways: (1) the inhibition of gonadotropin release and/or synthesis, (2) the interference with testosterone and/or dihydrotestosterone biosynthesis, (3) the blocking of protein synthesis, and (4) the competition with androgens at receptor sites. Although the major reason for the development of antiandrogens is to utilize them in certain clinical situations, some have become important tools in studying androgen action, particularly on the molecular level. The clinical effectiveness of some antiandrogens in prostatic hyperplasias, hirsutism, and acne represents an important advance in therapeutics, but the search for more potent antiandrogens with minimal side effects should continue.

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