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在正常男性中,通过每日注射促性腺激素释放激素(GnRH)拮抗剂西曲瑞克,持续8天抑制血清促黄体生成素(LH)、促卵泡生成素(FSH)和睾酮,并增加高密度脂蛋白胆固醇。

Sustained suppression of serum LH, FSH and testosterone and increase of high-density lipoprotein cholesterol by daily injections of the GnRH antagonist cetrorelix over 8 days in normal men.

作者信息

Behre H M, Böckers A, Schlingheider A, Nieschlag E

机构信息

Institute of Reproductive Medicine, University (WHO Collaborating Center for Research in Human Reproduction), Münster, Germany.

出版信息

Clin Endocrinol (Oxf). 1994 Feb;40(2):241-8. doi: 10.1111/j.1365-2265.1994.tb02475.x.

Abstract

OBJECTIVE

Recently we have shown that single dose injections of the new GnRH antagonist cetrorelix ([Ac-D-Na(2)1, D-Phe(4Cl)2, D-Pal(3)3, D-Cit6, D-Ala]GnRH; SB-75) decrease serum LH and testosterone in a dose-dependent manner in normal men. These results prompted us to investigate the effectiveness and safety of multiple daily injections of cetrorelix in normal male volunteers.

DESIGN AND VOLUNTEERS

Following two control examinations 16 young men were randomly assigned to four study groups (n = 4/group). Daily doses of 0 (placebo), 2, 5, and 10 mg cetrorelix were injected subcutaneously at 0800 h for 8 days and morning and evening blood samples were obtained for 3 weeks.

RESULTS

One day after the first cetrorelix injection, serum LH and testosterone concentrations were significantly suppressed in all treatment groups. Whereas in the 2 and 5-mg dose groups LH and testosterone showed some fluctuations, daily injections of 10 mg cetrorelix consistently suppressed LH and testosterone in all men. In addition, in this group serum FSH concentrations were significantly suppressed to subnormal values 1 day after the first injection and remained in this range up to 5 days after the last injection. A time and dose-dependent increase of high-density lipoprotein cholesterol was observed during cetrorelix-induced testosterone deprivation with a maximal increase of 0.38 +/- 0.13 mmol/l (14.8 +/- 5.1 mg/dl; mean +/- SEM) in the 10-mg dose group. In addition, parallel to suppressed testosterone the volunteers' libido was significantly reduced under the GnRH antagonist. Apart from those symptoms caused by androgen deficiency, the only adverse side-effect observed was a mild painless local erythema at the injection site that disappeared within an hour.

CONCLUSIONS

Daily injections of 10 mg cetrorelix effectively and consistently suppress serum LH, FSH and testosterone concentrations, and therefore it has potential for treatment of sex hormone-dependent diseases and for male contraception.

摘要

目的

最近我们发现,单次注射新型促性腺激素释放激素(GnRH)拮抗剂西曲瑞克([Ac-D-Na(2)1, D-Phe(4Cl)2, D-Pal(3)3, D-Cit6, D-Ala]GnRH;SB-75)可使正常男性的血清促黄体生成素(LH)和睾酮呈剂量依赖性降低。这些结果促使我们研究在正常男性志愿者中每日多次注射西曲瑞克的有效性和安全性。

设计与志愿者

在进行两次对照检查后,16名年轻男性被随机分为四个研究组(每组n = 4)。每日0(安慰剂)、2、5和10毫克西曲瑞克剂量于08:00皮下注射,共8天,并在3周内每天早晚采集血样。

结果

首次注射西曲瑞克一天后,所有治疗组的血清LH和睾酮浓度均受到显著抑制。2毫克和5毫克剂量组的LH和睾酮出现一些波动,而每日注射10毫克西曲瑞克可使所有男性的LH和睾酮持续受到抑制。此外,在该组中,首次注射1天后血清促卵泡生成素(FSH)浓度显著降低至低于正常水平,并在最后一次注射后5天内维持在该范围内。在西曲瑞克诱导睾酮缺乏期间,观察到高密度脂蛋白胆固醇呈时间和剂量依赖性增加,10毫克剂量组最大增加0.38 +/- 0.13毫摩尔/升(14.8 +/- 5.1毫克/分升;平均值 +/- 标准误)。此外,与睾酮受到抑制同时,GnRH拮抗剂使志愿者的性欲显著降低。除雄激素缺乏引起的症状外,观察到的唯一不良副作用是注射部位出现轻度无痛性局部红斑,1小时内消失。

结论

每日注射10毫克西曲瑞克可有效且持续地抑制血清LH、FSH和睾酮浓度,因此其在治疗性激素依赖性疾病和男性避孕方面具有潜力。

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