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麦角酸二乙酰胺与阿扑吗啡对雌性大鼠交配反应作用的比较。

Comparison of the action of lysergic acid diethylamide and apomorphine on the copulatory response in the female rat.

作者信息

Eliasson M, Meyerson B J

出版信息

Psychopharmacology (Berl). 1976 Sep 29;49(3):301-6. doi: 10.1007/BF00426833.

Abstract

The effects of lysergic acid diethylamide (LSD) and apomorphine were compared using female copulatory behavior (lordosis response), in ovariectomized estrogen + progesterone-treated rats. Both serotonin and dopamine are implicated in the inhibition of this behavior. Each compound inhibited lordosis behavior dose dependently and with a similar time-course. Pimozide (0.1; 0.5 mg/kg) blocked the apomorphine (0.2 mg/kg)-induced decrease of lordosis response, while only a certain abbreviation of the LSD (0.10 mg/kg) inhibition was achieved by pimozide (0.5 mg/kg). Chlorpromazine (0.5 mg/kg) in a dose without effects on lordosis of its own had an action similar to pimozide on the LSD effect. It is concluded that the predominant action of LSD on the female copulatory response is not mediated by increased dopamine receptor activity but that the LSD effect might be modulated by decreased dopaminergic activity.

摘要

在切除卵巢并用雌激素 + 孕酮处理的大鼠中,利用雌性交配行为(脊柱前凸反应)比较了麦角酸二乙酰胺(LSD)和阿扑吗啡的作用。5-羟色胺和多巴胺都与这种行为的抑制有关。每种化合物均剂量依赖性地抑制脊柱前凸行为,且时间进程相似。匹莫齐特(0.1;0.5毫克/千克)可阻断阿扑吗啡(0.2毫克/千克)诱导的脊柱前凸反应降低,而匹莫齐特(0.5毫克/千克)仅使LSD(0.10毫克/千克)的抑制作用有一定程度的缩短。氯丙嗪(0.5毫克/千克)在对脊柱前凸本身无影响的剂量下,对LSD效应的作用与匹莫齐特相似。得出的结论是,LSD对雌性交配反应的主要作用不是通过增加多巴胺受体活性介导的,而是LSD效应可能通过降低多巴胺能活性来调节。

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