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睾酮与一种新型强效促性腺激素释放激素拮抗剂对正常男性促性腺激素和抑制素水平抑制作用的比较。

A comparison of the suppressive effects of testosterone and a potent new gonadotropin-releasing hormone antagonist on gonadotropin and inhibin levels in normal men.

作者信息

Bagatell C J, McLachlan R I, de Kretser D M, Burger H G, Vale W W, Rivier J E, Bremner W J

机构信息

Medical Service, Veterans Administration Medical Center, Seattle, Washington 98108.

出版信息

J Clin Endocrinol Metab. 1989 Jul;69(1):43-8. doi: 10.1210/jcem-69-1-43.

DOI:10.1210/jcem-69-1-43
PMID:2499592
Abstract

GnRH antagonists have been developed in large part because of their potential use as contraceptive agents, particularly in men. Specifically, it was hoped that GnRH antagonists combined with testosterone (T) would be a more effective contraceptive regimen than T alone. We compared the suppressive effects of a potent GnRH antagonist, Na1-Glu [AcD2NaL1,D4ClPhe2,D3Pal3,Arg5,DGlu6(AA),+ ++DAla10-GnRH], and of T together and separately on serum and urinary gonadotropin and serum inhibin levels in normal men. Ten-day courses of Nal-Glu (75 micrograms/kg; Nal-Glu alone), 200 mg testosterone enanthate, im, on days 0 and 7 (T alone), and the combination (Na1-Glu + T) were given to nine men. Serum gonadotropin and inhibin concentrations decreased after 1-2 days of Na1-Glu administration, while gonadotropin suppression occurred more slowly after T alone. Serum T fell to 30% of baseline values during Na1-Glu administration. The combination of Na1-Glu + T was more effective in suppressing serum LH, FSH, and inhibin than was either Na1-Glu alone or T alone. All hormone levels returned to baseline levels within 2.5 weeks after the end of the three regimens. We conclude that the Na1-Glu GnRH antagonist effectively inhibits gonadotropin, inhibin, and sex steroid secretion when given daily for 10 days and that the administration of Nal-Glu + T results in more complete gonadotropin and gonadal suppression than that produced by either agent given alone. These results encourage further investigation of the combination of a GnRH antagonist and T as a male contraceptive regimen and of the antagonist alone as a treatment for hormone-dependent neoplasia.

摘要

促性腺激素释放激素(GnRH)拮抗剂的研发很大程度上是因其有望用作避孕药物,尤其是对男性而言。具体来说,人们希望GnRH拮抗剂与睾酮(T)联合使用会比单独使用T成为更有效的避孕方案。我们比较了一种强效GnRH拮抗剂Na1-Glu [AcD2NaL1,D4ClPhe2,D3Pal3,Arg5,DGlu6(AA),+++DAla10-GnRH] 单独及与T联合使用时,对正常男性血清和尿促性腺激素以及血清抑制素水平的抑制作用。九名男性接受了为期十天的治疗:第0天和第7天肌肉注射200mg庚酸睾酮(单独使用T);每天注射75微克/千克的Na1-Glu(单独使用Na1-Glu);以及联合使用(Na1-Glu + T)。注射Na1-Glu 1-2天后,血清促性腺激素和抑制素浓度下降,而单独使用T后促性腺激素抑制作用出现得较慢。注射Na1-Glu期间,血清T降至基线值的30%。与单独使用Na1-Glu或单独使用T相比,Na1-Glu + T联合使用在抑制血清促黄体生成素(LH)、促卵泡生成素(FSH)和抑制素方面更有效。三种治疗方案结束后2.5周内,所有激素水平均恢复到基线水平。我们得出结论,每天注射10天,Na1-Glu GnRH拮抗剂可有效抑制促性腺激素、抑制素和性类固醇的分泌,并且与单独使用任何一种药物相比,联合使用Na1-Glu + T可导致更完全的促性腺激素和性腺抑制。这些结果鼓励进一步研究GnRH拮抗剂与T联合作为男性避孕方案,以及单独使用拮抗剂治疗激素依赖性肿瘤。

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