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卵巢类固醇与雌性大鼠吗啡诱导的镇痛和僵住症的调节

Ovarian steroids and modulation of morphine-induced analgesia and catalepsy in female rats.

作者信息

Banerjee P, Chatterjee T K, Ghosh J J

出版信息

Eur J Pharmacol. 1983 Dec 23;96(3-4):291-4. doi: 10.1016/0014-2999(83)90319-9.

Abstract

The influence of ovarian steroids on modulation of antinociceptive and cataleptic responses to morphine in female rats was evaluated. The sensitivity of the animals to morphine varied at different stages of the estrous cycle. The responses of postpartum and ovariectomized rats to morphine was attenuated. The test doses of estradiol-17 beta or progesterone, either alone or in combination, did not alter this attenuated morphine sensitivity. Testosterone, however, sensitized post-partum as well as ovariectomized rats to morphine. Unlike progesterone, 17-alpha-hydroxy progesterone antagonized testosterone. Collectively these data implicate ovarian testosterone as a physiological modulator of actions of morphine in female rats.

摘要

评估了卵巢甾体激素对雌性大鼠吗啡抗伤害感受和木僵反应调节的影响。动物对吗啡的敏感性在发情周期的不同阶段有所变化。产后和去卵巢大鼠对吗啡的反应减弱。单独或联合使用的雌二醇-17β或孕酮的测试剂量并未改变这种减弱的吗啡敏感性。然而,睾酮使产后和去卵巢大鼠对吗啡敏感。与孕酮不同,17-α-羟孕酮拮抗睾酮。总体而言,这些数据表明卵巢睾酮是雌性大鼠吗啡作用的生理调节剂。

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