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促性腺激素释放激素拮抗剂的药理学及潜在应用。

The pharmacology and the potential applications of GnRH antagonists.

作者信息

Loy R A

机构信息

Center for Infertility and Reproductive Medicine, Orlando, Florida.

出版信息

Curr Opin Obstet Gynecol. 1994 Jun;6(3):262-8.

PMID:8038414
Abstract

Gonadotropin-releasing hormone (GnRH) antagonists are potent analogs of native GnRH. As biochemical probes, these recently developed compounds have allowed for profound insights into the physiology of the pituitary-ovarian and pituitary-testicular axes; as therapeutic alternatives, the GnRH antagonists hold great promise for various clinical applications, including contraception, ovulation induction, precocious puberty, and gonadal steroid-dependent neoplasia. Indeed, because of intrinsic mechanistic differences, the antagonists hold certain practical advantages over the GnRH agonists.

摘要

促性腺激素释放激素(GnRH)拮抗剂是天然GnRH的强效类似物。作为生化探针,这些最近开发的化合物使人们对垂体-卵巢轴和垂体-睾丸轴的生理学有了深刻的认识;作为治疗选择,GnRH拮抗剂在包括避孕、促排卵、性早熟和性腺类固醇依赖性肿瘤等各种临床应用中具有很大的前景。事实上,由于内在的机制差异,拮抗剂相对于GnRH激动剂具有某些实际优势。

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