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GnRH类似物长期抑制睾丸功能期间类固醇对hCG反应性的动力学

Kinetics of steroid responsiveness to hCG during chronic inhibition of testicular function by GnRH analogue.

作者信息

Vicari E, Mongioì A, Aliffi A, Gulizia S, D'Agata R

出版信息

Acta Endocrinol (Copenh). 1984 Dec;107(4):544-9. doi: 10.1530/acta.0.1070544.

Abstract

The effect of daily injections of D-Ser-(TBU)6-LRH-EA10 (GnRH analogue (GnRH-A) 100 micrograms sc) on serum testosterone (T), 17 alpha-hydroxyprogesterone (17OHP) and oestradiol-17 beta (E2) was studied in 4 men. During GnRH-A therapy T, 17OHP and E2 were markedly decreased by the end of the second month. Continuous long-term administration of GnRh-A inhibited testicular function. To test whether the biosynthetic pathway was affected by the regimen, a bolus of 2000 U hCG was given to each subject after 10 months of therapy. Evaluation of the kinetics of steroid responsiveness showed a significant release of T in response to the trophic stimulus, with little or no elevation of serum 17OHP and E2. The response seen in these treated men appeared similar to that found in hypogonadotrophic men and prepubertal boys.

摘要

在4名男性中研究了每日注射D-丝氨酸-(叔丁基)6-亮丙瑞林-醋酸(GnRH类似物(GnRH-A)100微克皮下注射)对血清睾酮(T)、17α-羟孕酮(17OHP)和雌二醇-17β(E2)的影响。在GnRH-A治疗期间,到第二个月末,T、17OHP和E2显著降低。持续长期给予GnRh-A抑制睾丸功能。为了测试生物合成途径是否受该方案影响,在治疗10个月后给每个受试者静脉注射2000U人绒毛膜促性腺激素(hCG)。对类固醇反应动力学的评估显示,对促性腺刺激有显著的T释放,血清17OHP和E2几乎没有升高或没有升高。在这些接受治疗的男性中观察到的反应与在促性腺激素缺乏男性和青春期前男孩中发现的反应相似。

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