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性腺类固醇对去性腺大鼠纳洛酮诱导的促黄体生成素分泌的影响比较。

A comparison of the effects of gonadal steroids on naloxone-induced LH secretion in gonadectomized rats.

作者信息

Spencer G M, Whitehead S A

出版信息

J Endocrinol. 1986 Aug;110(2):327-34. doi: 10.1677/joe.0.1100327.

Abstract

The effects of the opiate antagonist naloxone on serum LH concentrations was investigated in gonadectomized rats given different regimes of steroid pretreatment. Two injections of testosterone given 48 and 24 h before naloxone treatment failed to reinstate LH responses to this drug in castrated rats while subcutaneous testosterone-filled silicone elastomer capsules implanted for a week were effective in this respect. Injections of oestrogen, oestrogen plus progesterone or progesterone alone all restored LH responses to naloxone in ovariectomized rats when given 48 and/or 24 h before drug treatment, although the magnitude of these responses varied according to the precise steroid treatments. The hypothalamic-pituitary axis was also responsive to naloxone just before the progesterone-induced LH surge in oestrogen-primed ovariectomized rats. Results show that gonadal steroids are permissive to the effects of opiate drugs, but they suggest that endogenous opioid systems do not necessarily mediate the negative feedback effects of steroids. Some other factor(s), as yet unidentified in the rat, may control the opioid modulation of gonadotrophin secretion or exert an independent inhibitory effect on gonadotrophin release.

摘要

在接受不同类固醇预处理方案的去性腺大鼠中,研究了阿片类拮抗剂纳洛酮对血清促黄体生成素(LH)浓度的影响。在纳洛酮治疗前48小时和24小时注射两次睾酮,未能恢复去势大鼠对该药物的LH反应,而皮下植入含睾酮的硅胶弹性体胶囊一周在这方面是有效的。在药物治疗前48小时和/或24小时注射雌激素、雌激素加孕酮或单独注射孕酮,均可恢复去卵巢大鼠对纳洛酮的LH反应,尽管这些反应的程度因具体的类固醇治疗而异。在雌激素预处理的去卵巢大鼠中,就在孕酮诱导的LH峰之前,下丘脑-垂体轴也对纳洛酮有反应。结果表明,性腺类固醇允许阿片类药物发挥作用,但提示内源性阿片系统不一定介导类固醇的负反馈作用。大鼠中尚未确定的某些其他因素可能控制促性腺激素分泌的阿片类调节,或对促性腺激素释放发挥独立的抑制作用。

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