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抗雄激素

Antiandrogens.

作者信息

Neri R O

出版信息

Adv Sex Horm Res. 1976;2:233-62.

PMID:65117
Abstract

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.

摘要

许多抗雄激素药物,主要是甾体类药物和一些非甾体类药物,已被合成并在多种可用的生物学检测中进行了测试。不幸的是,这些化合物中的许多都具有其他生物学活性,这使得难以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多种方式实现:(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。尽管开发抗雄激素药物的主要原因是在某些临床情况下使用它们,但有些已成为研究雄激素作用的重要工具,特别是在分子水平上。一些抗雄激素药物在前列腺增生、多毛症和痤疮方面的临床疗效代表了治疗学上的一项重要进展,但寻找更有效且副作用最小的抗雄激素药物的工作应继续进行。

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