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γ-氨基丁酸能药物对阿扑吗啡诱导的大鼠阴茎勃起的影响。

Effects of GABA-ergic drugs on penile erection induced by apomorphine in rats.

作者信息

Zarrindast M R, Farahvash H

机构信息

Department of Pharmacology, School of Medicine, University of Tehran, Iran.

出版信息

Psychopharmacology (Berl). 1994 Jun;115(1-2):249-53. doi: 10.1007/BF02244779.

Abstract

The effects of GABA agonists and antagonists on penile erection (PE) induced by apomorphine were investigated in rats. Subcutaneous (SC) administration of apomorphine (0.01-0.1 mg/kg) induces a dose-dependent PE in rats. The maximum effect was obtained with 0.1 mg/kg of the drug. The response was decreased with increasing doses of apomorphine from 0.1 to 0.5 mg/kg. The response induced by apomorphine (0.1-0.5 mg/kg) was decreased in animals pretreated with either the GABA-A agonist muscimol or the GABA-B agonist baclofen. Combination of muscimol with baclofen caused a stronger inhibitory effect on apomorphine-induced PE. Bicuculline or picrotoxin but not phaclofen reduced the inhibitory effect of muscimol on PE induced by apomorphine, whereas phaclofen but not GABA-A antagonists decreased the inhibitory action of baclofen on apomorphine-induced PE. Pretreatment of animals with higher doses of the GABA-A antagonists bicuculline and picrotoxin or the GABA-B antagonist phaclofen elicited inhibition of apomorphine-induced PE. However, the inhibitory effects of GABA-A and GABA-B antagonists are lost on combination. Administration of GABA-A and GABA-B receptor stimulation inhibit PE induced by dopaminergic mechanism(s).

摘要

在大鼠中研究了γ-氨基丁酸(GABA)激动剂和拮抗剂对阿扑吗啡诱导的阴茎勃起(PE)的影响。皮下注射阿扑吗啡(0.01 - 0.1毫克/千克)可在大鼠中诱导剂量依赖性的阴茎勃起。给予0.1毫克/千克的该药物可获得最大效应。随着阿扑吗啡剂量从0.1毫克/千克增加到0.5毫克/千克,反应减弱。在用GABA - A激动剂蝇蕈醇或GABA - B激动剂巴氯芬预处理的动物中,阿扑吗啡(0.1 - 0.5毫克/千克)诱导的反应减弱。蝇蕈醇与巴氯芬联合使用对阿扑吗啡诱导的阴茎勃起产生更强的抑制作用。荷包牡丹碱或印防己毒素而非氯苯氨丁酸可降低蝇蕈醇对阿扑吗啡诱导的阴茎勃起的抑制作用,而氯苯氨丁酸而非GABA - A拮抗剂可降低巴氯芬对阿扑吗啡诱导的阴茎勃起的抑制作用。用较高剂量的GABA - A拮抗剂荷包牡丹碱和印防己毒素或GABA - B拮抗剂氯苯氨丁酸预处理动物可抑制阿扑吗啡诱导的阴茎勃起,但GABA - A和GABA - B拮抗剂联合使用时抑制作用消失。给予GABA - A和GABA - B受体刺激可抑制多巴胺能机制诱导的阴茎勃起。

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