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达那唑作为一种黄体溶解剂。

Danazol as a luteolytic agent.

作者信息

Wentz A C, Sapp K C

出版信息

Fertil Steril. 1978 Jan;29(1):23-5.

PMID:620838
Abstract

Danazol, a synthetic 2,3-isoxazol derivative of 17 alpha-ethinyltestosterone, was administered to healthy nonpregnant volunteers to determine wheter a luteolytic effect could be detected by observation of cycle length, duration of the luteal rise, and luteal steroidogenesis. Danazol administration resulted in a decreased duration of the luteal rise and a decrease in progesterone output in three of four subjects, but no decrease in total cycle length. The administration of human chorionic gonadotropin during danazol administration increased progesterone output. Therefore, danazol would be unlikely to be effective as a luteolytic contraceptive agent.

摘要

达那唑是17α-乙炔睾酮的一种合成2,3-异恶唑衍生物,被给予健康未怀孕的志愿者,以通过观察月经周期长度、黄体期上升持续时间和黄体类固醇生成来确定是否能检测到黄体溶解作用。服用达那唑导致四名受试者中有三名黄体期上升持续时间缩短且孕酮分泌减少,但月经周期总长度未缩短。在服用达那唑期间注射人绒毛膜促性腺激素可增加孕酮分泌。因此,达那唑不太可能作为一种黄体溶解避孕剂有效。

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