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5α-双氢睾酮和抗雄激素对去势大鼠垂体中5α-还原酶和3α-羟基类固醇脱氢酶活性的作用。

The action of 5 alpha-dihydrotestosterone and antiandrogens on the activities of 5 alpha-reductase and 3 alpha-hydroxysteroid dehydrogenase in the pituitary gland of gonadectomized rats.

作者信息

Ghraf R, Schneider K, Kirchhoff J, Hiemke C

出版信息

J Steroid Biochem. 1982 Apr;16(4):545-52. doi: 10.1016/0022-4731(82)90077-2.

Abstract

In gonadectomized rats of either sex s.c. administration of 5 alpha-dihydrotestosterone (DHT) reversed, in a dose dependent manner, effects brought about by gonadectomy: it decreased pituitary wet weight and serum levels of LH and FSH and suppressed microsomal enzyme activities involved in testosterone and progesterone metabolism in the pituitary gland, NADPH-linked 5 alpha-reductase and NADH-linked 3 alpha-hydroxysteroid dehydrogenase (3 alpha-HSDH). Concomitantly administered nonsteroidal antiandrogen, flutamide (5 mg/day), antagonized some of the suppressive effects induced by a 14-day treatment of gonadectomized rats with high dose (1 mg/day) of DHT. It completely blocked DHT action on pituitary 5 alpha-reductase activity in the female rat and, in the male, inhibition was found to be 30-35%. In male, but not female rats, it completely blocked DHT suppression of serum FSH level whereas it slightly, but significantly inhibited DHT suppression of serum LH in rats of either sex. However, flutamide did not prevent DHT suppression of pituitary wet weight or NADH-linked 3 alpha-HSDH activity. Concomitantly administered progestational antiandrogen, cyproterone acetate (5 mg/day), inhibited DHT-induced weight increase of seminal vesicles by 50-55% and completely blocked the weight decrease of pituitary gland but did not antagonize DHT suppression of serum gonadotropins or pituitary enzyme activities. The results obtained with flutamide suggest that DHT-induced suppression of pituitary NADPH-linked 5 alpha-reductase, but not NADH-linked 3 alpha-HSDH activity, might involve an androgen receptor mechanism.

摘要

在去性腺的雄性或雌性大鼠中,皮下注射5α - 双氢睾酮(DHT)可呈剂量依赖性地逆转去性腺所带来的影响:它降低了垂体湿重以及血清中促黄体生成素(LH)和促卵泡生成素(FSH)的水平,并抑制了垂体中参与睾酮和孕酮代谢的微粒体酶活性,即烟酰胺腺嘌呤二核苷酸磷酸(NADPH)连接的5α - 还原酶和烟酰胺腺嘌呤二核苷酸(NADH)连接的3α - 羟基类固醇脱氢酶(3α - HSDH)。同时给予非甾体类抗雄激素药物氟他胺(5毫克/天),可拮抗高剂量(1毫克/天)DHT对去性腺大鼠进行14天治疗所诱导的一些抑制作用。它完全阻断了DHT对雌性大鼠垂体5α - 还原酶活性的作用,而在雄性大鼠中,发现抑制率为30 - 35%。在雄性大鼠而非雌性大鼠中,它完全阻断了DHT对血清FSH水平的抑制作用,而在两种性别的大鼠中,它略微但显著地抑制了DHT对血清LH的抑制作用。然而,氟他胺并未阻止DHT对垂体湿重或NADH连接的3α - HSDH活性的抑制作用。同时给予孕激素类抗雄激素药物醋酸环丙孕酮(5毫克/天),可抑制DHT诱导的精囊重量增加50 - 55%,并完全阻断垂体重量的减轻,但并未拮抗DHT对血清促性腺激素或垂体酶活性的抑制作用。用氟他胺获得的结果表明,DHT诱导的对垂体NADPH连接的5α - 还原酶的抑制作用,而非NADH连接的3α - HSDH活性,可能涉及雄激素受体机制。

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