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右旋苯丙胺和芬氟拉明对大鼠孕酮诱导的促黄体生成素和催乳素释放的阻断作用。

Blockage of progesterone-induced release of luteinizing hormone and prolactin by d-amphetamine and fenfluramine in rats.

作者信息

Donoso A O

出版信息

Psychopharmacology (Berl). 1977 Dec 19;55(2):173-6. doi: 10.1007/BF01457854.

Abstract

Subcutaneous administration of d-amphetamine at various doses (1.25, 2.5, and 5 mg/kg) decreased plasma luteinizing-hormone levels in ovariectomized rats primed with estradiol and injected with progesterone. In these animals prolactin levels decreased after injection of 0.6 and 1.25 mg/kg of d-amphetamine. No significant hormone modifications were detected in oavariectomized and ovariectomized estradiol-primed rats after injection of 2.5 mg/kg of d-amphetamine. Fenfluramine at doses of 25 mg/kg induced decreases of plasma LH and prolactin levels in ovariectomized estradiol- and progesterone-treated rats. A low dose of fenfluramine, 2.5 mg/kg, had no effect. It is concluded that d-amphetamine and fenfluramine are able to alter the facilitatory actions of progesterone on luteinizing hormone and prolactin release in ovariectomized estradiol-primed rats.

摘要

对用雌二醇预处理并注射孕酮的去卵巢大鼠皮下注射不同剂量(1.25、2.5和5毫克/千克)的右旋苯丙胺,会降低其血浆促黄体生成素水平。在这些动物中,注射0.6和1.25毫克/千克右旋苯丙胺后,催乳素水平降低。注射2.5毫克/千克右旋苯丙胺后,在去卵巢大鼠和用雌二醇预处理的去卵巢大鼠中未检测到显著的激素变化。在去卵巢、经雌二醇和孕酮处理的大鼠中,25毫克/千克剂量的芬氟拉明可导致血浆促黄体生成素和催乳素水平降低。低剂量(2.5毫克/千克)的芬氟拉明没有效果。得出的结论是,右旋苯丙胺和芬氟拉明能够改变孕酮对去卵巢、经雌二醇预处理大鼠促黄体生成素和催乳素释放的促进作用。

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