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肾上腺素能拮抗剂对短期去卵巢并用类固醇预处理大鼠促黄体生成素激增的影响。

Effects of adrenergic antagonists on LH surge in short-term ovariectomized-steroids-primed rats.

作者信息

Pi W P

机构信息

Department of Physiology, College of Medicine, National Taiwan University, Taipei, R.O.C.

出版信息

Proc Natl Sci Counc Repub China B. 1999 Jul;23(3):120-5.

Abstract

Characterization of adrenergic stimuli on luteinizing hormone (LH) release induced by ovarian steroids in short-term ovariectomized (OVX) rats was studied. Female Sprague-Dawley rats were OVX about 1000 h on the diestrous day 1. After ovariectomy, rats were immediately inserted estradiol-containing Silastic capsules s.c. and implanted atrial Silastic tubing for frequent blood samplings. All the rats received 2 mg of progesterone s.c. at 0930 h the next morning. At 1200 h, the rats received additional treatments: a saline vehicle, prazosin HC1 (an alpha 1-adrenergic antagonist), yohimbine HC1 (an alpha 2-adrenergic antagonist), or propranolol HC1 (a beta-adrenergic antagonist) s.c., respectively. Two different doses of individual adrenergic antagonists were used on an equimolar basis in order to show their effectiveness on steroids-induced LH secretion. Blood samples were collected before and 1, 3, and 5 hours after the treatments through indwelt tubings. LH surge induced by ovarian steroids was suppressed/delayed by prazosin and yohimbine, but potentiated by propranolol in a dose-dependent manner. Results suggested that the hypothalamic alpha 1-, alpha 2-, and beta-adrenoreceptors were involved in the control of LH surge in the short-term OVX-steroids-primed rats. Principally, the alpha 1- and alpha 2-adrenoreceptors played a facilitatory role, and the beta-adrenoreceptors played an inhibitory role in the regulation of LH surge induced by ovarian steroids.

摘要

研究了去卵巢(OVX)短期大鼠中,肾上腺素能刺激对卵巢类固醇诱导的促黄体生成素(LH)释放的影响。雌性斯普拉格-道利大鼠在动情周期第1天约1000小时进行去卵巢手术。去卵巢后,大鼠立即皮下植入含雌二醇的硅橡胶胶囊,并植入心房硅橡胶管以便频繁采血。所有大鼠于次日上午0930皮下注射2mg孕酮。1200时,大鼠分别接受额外处理:生理盐水、盐酸哌唑嗪(一种α1肾上腺素能拮抗剂)、盐酸育亨宾(一种α2肾上腺素能拮抗剂)或盐酸普萘洛尔(一种β肾上腺素能拮抗剂),均为皮下注射。以等摩尔浓度使用两种不同剂量的各肾上腺素能拮抗剂,以显示它们对类固醇诱导的LH分泌的作用效果。通过留置管在处理前以及处理后1、3和5小时采集血样。卵巢类固醇诱导的LH峰被哌唑嗪和育亨宾抑制/延迟,但被普萘洛尔以剂量依赖性方式增强。结果表明,下丘脑α1、α2和β肾上腺素能受体参与了短期去卵巢-类固醇预处理大鼠LH峰的调控。主要地,α1和α2肾上腺素能受体在卵巢类固醇诱导的LH峰调节中起促进作用,而β肾上腺素能受体起抑制作用。

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