Serum levels of follicle-stimulating hormone and luteinizing hormone after subcutaneous administration of human menopausal gonadotropin during pituitary suppression.

I J Duijkers, Y M Magnusson, H M Hollanders
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Abstract

Objective: The present study investigated the pharmacokinetics of a single subcutaneous dose of human menopausal gonadotropin (hMG) on serum follicle-stimulating hormone (FSH) and luteinizing hormone (LH) concentrations.

Subjects and methods: Six healthy female volunteers, aged 20-40 years, with regular menstrual cycles and normal endocrine profiles, who were not receiving any hormonal medication, were treated with the gonadotropin-releasing-hormone agonist buserelin to suppress endogenous gonadotropin release. One volunteer dropped out during treatment. When the serum estradiol concentration had fallen to below 500 pmol/L, an injection of 150 IU hMG (HumegonR) was given subcutaneously. Immediately before injection and 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 15, 20, 24, 48 and 96 hours after, blood samples were drawn for determination of FSH and LH concentrations.

Results: The baseline FSH level was 2.8 IU/L, and peak concentration (6.8 IU/L) was reached 12 hours after hMG injection (median values). Exogenous LH could not be measured because of the presence of endogenous LH.

Discussion: The pattern of serum FSH concentrations after a single injection of hMG was found to resemble that seen after intramuscular hMG administration, although the peak FSH value was reached somewhat later.

垂体抑制期间皮下注射促性腺激素后血清促卵泡激素和黄体生成素水平。
目的:研究单次皮下剂量人绝经期促性腺激素(hMG)对血清促卵泡激素(FSH)和黄体生成素(LH)浓度的药代动力学。受试者与方法:6名健康女性志愿者,年龄20-40岁,月经周期规律,内分泌正常,未接受任何激素药物治疗,应用促性腺激素释放激素激动剂布瑟林抑制内源性促性腺激素释放。一名志愿者在治疗期间退出。当血清雌二醇浓度降至500 pmol/L以下时,皮下注射150 IU hMG (HumegonR)。于注射前及注射后0.5、1、2、3、4、6、8、10、12、15、20、24、48、96小时抽取血液,测定卵泡刺激素和黄体生成素浓度。结果:FSH基线水平为2.8 IU/L,注射hMG后12 h达到峰值(6.8 IU/L)(中位数)。由于存在内源性LH,因此无法测量外源性LH。讨论:发现单次注射hMG后血清FSH浓度模式与肌肉注射hMG后相似,尽管FSH峰值达到的时间稍晚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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