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皮质酮对成年雄性大鼠睾丸酮、5α-二氢睾丸酮和雌二醇负反馈作用的影响

Effects of corticosterone on the negative feedback action of testosterone, 5 alpha-dihydrotestosterone and estradiol in the adult male rat.

作者信息

Vreeburg J T, Samaun K, Verkade H J, Verhoef P, Ooms M P, Weber R F

机构信息

Department of Endocrinology, Growth and Reproduction, Erasmus University, Rotterdam, The Netherlands.

出版信息

J Steroid Biochem. 1988 Jan;29(1):93-8. doi: 10.1016/0022-4731(88)90381-0.

Abstract

Corticosterone acetate (10 mg/day) was administered to gonadectomized and adrenalectomized male rats bearing 5, 10 or 15 mm long testosterone filled silicone elastomer capsules. It was found that the serum testosterone levels induced by these capsules were not influenced by corticosterone treatment and that the weights of the prostates in the corticosterone treated rats were not different from their controls. In contrast, corticosterone acetate increased markedly the LH and FSH inhibitory effects of testosterone. Since several brain structures are able to convert testosterone into 17-beta-hydroxy-5-alpha-androstan-3-one (5-alpha-dihydrotestosterone) and/or estradiol, and these metabolites are probably involved in mechanisms controlling gonadotropin secretion, we studied also the effects of corticosterone on the feedback action of dihydrotestosterone and estradiol. 5 alpha-Dihydrotestosterone was administered by 5, 10 or 20 mm long elastomere capsules whereas estradiol was given by daily s.c. injections of 0.125, 0.25 or 0.50 micrograms estradiol benzoate. In the presence of corticosterone acetate the gonadotropin inhibitory action of testosterone, 5 alpha-dihydrotestosterone and estradiol increased more than 2 times.

摘要

给摘除性腺和肾上腺的雄性大鼠植入5、10或15毫米长的填充睾酮的硅橡胶弹性体胶囊,并给予醋酸皮质酮(10毫克/天)。结果发现,这些胶囊诱导的血清睾酮水平不受皮质酮治疗的影响,且接受皮质酮治疗的大鼠前列腺重量与其对照组无差异。相比之下,醋酸皮质酮显著增强了睾酮对促黄体生成素(LH)和促卵泡生成素(FSH)的抑制作用。由于几个脑区能够将睾酮转化为17-β-羟基-5-α-雄甾烷-3-酮(5-α-双氢睾酮)和/或雌二醇,且这些代谢产物可能参与控制促性腺激素分泌的机制,我们还研究了皮质酮对双氢睾酮和雌二醇反馈作用的影响。通过5、10或20毫米长的弹性体胶囊给予5-α-双氢睾酮,而通过每日皮下注射0.125、0.25或0.50微克苯甲酸雌二醇给予雌二醇。在醋酸皮质酮存在的情况下,睾酮、5-α-双氢睾酮和雌二醇对促性腺激素的抑制作用增加了两倍多。

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