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高剂量缓释促黄体生成素释放激素激动剂(布舍瑞林)联合口服睾酮抑制男性生育功能失败。

Failure of high-dose sustained release luteinizing hormone releasing hormone agonist (buserelin) plus oral testosterone to suppress male fertility.

作者信息

Michel E, Bents H, Akhtar F B, Hönigl W, Knuth U A, Sandow J, Nieschlag E

出版信息

Clin Endocrinol (Oxf). 1985 Dec;23(6):663-75. doi: 10.1111/j.1365-2265.1985.tb01127.x.

DOI:10.1111/j.1365-2265.1985.tb01127.x
PMID:3938352
Abstract

Previously we have demonstrated that sperm counts of normal young men decreased during constant subcutaneous infusion of the LHRH agonist buserelin (118 or 230 micrograms/d). In order to test whether azoospermia can be achieved with higher doses, seven young men received 450 micrograms buserelin subcutaneously daily for 12 weeks via extracorporeal osmotic minipumps. To avoid symptoms of androgen deficiency, oral supplementation with 80 mg/d testosterone undecanoate (TU) was initiated in week 5 and was increased to 120 mg/d by week 8. Follow-up after treatment lasted for another 12 weeks. In order to evaluate possible psychotropic effects of treatment-related endocrine changes, continuous psychometric testing was performed focusing on personality, emotions and sexuality. After an initial rise, both serum LH and FSH returned to normal. FSH was below normal during the 3rd-5th week following treatment. LHRH stimulation tests performed at the end of treatment showed pituitary desensitization. Serum T (always measured between 0800 and 1300 h at least 12 h after last TU) tended to decrease by week 7 and remained slightly depressed until the end of treatment while libido, potency and emotional well-being remained unchanged. While testicular volumes showed a reduction from week 7 of treatment to week 10 post-treatment, sperm counts decreased only insignificantly from 65 +/- 10 to 44 +/- 14 million per ml in week 12 post-treatment. Severe oligo- or azoospermia was not observed in any of the seven men. It is concluded that full androgen substitution by TU can drastically delay if not abolish the antifertility effect of LHRH-induced pituitary desensitization.

摘要

此前我们已经证明,在持续皮下输注促黄体生成素释放激素(LHRH)激动剂布舍瑞林(118或230微克/天)期间,正常年轻男性的精子计数会下降。为了测试更高剂量是否能导致无精子症,7名年轻男性通过体外渗透微型泵每天皮下注射450微克布舍瑞林,持续12周。为避免雄激素缺乏症状,在第5周开始口服补充80毫克/天的十一酸睾酮(TU),到第8周增加至120毫克/天。治疗后的随访持续了另外12周。为了评估治疗相关内分泌变化可能产生的精神影响,进行了持续的心理测试,重点关注人格、情绪和性功能。血清促黄体生成素(LH)和促卵泡生成素(FSH)在最初升高后均恢复正常。治疗后第3至5周FSH低于正常水平。治疗结束时进行的LHRH刺激试验显示垂体脱敏。血清睾酮(总是在最后一次TU注射至少12小时后的08:00至13:00之间测量)在第7周时趋于下降,并在治疗结束前一直略有降低,而性欲、性功能和情绪状态保持不变。虽然睾丸体积从治疗第7周开始至治疗后第10周有所减小,但治疗后第12周精子计数仅从65±10降至44±14百万/毫升,下降不显著。7名男性中无一例出现严重少精子症或无精子症。结论是,TU进行充分的雄激素替代即使不能消除LHRH诱导的垂体脱敏的抗生育作用,也能极大地延迟其作用。

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Failure of high-dose sustained release luteinizing hormone releasing hormone agonist (buserelin) plus oral testosterone to suppress male fertility.高剂量缓释促黄体生成素释放激素激动剂(布舍瑞林)联合口服睾酮抑制男性生育功能失败。
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