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低剂量阿扑吗啡对大鼠的辨别性刺激作用。

Discriminative stimulus effects of a low dose of apomorphine in the rat.

作者信息

Tang A H, Franklin S R

出版信息

Psychopharmacology (Berl). 1987;91(1):61-6. doi: 10.1007/BF00690928.

Abstract

The discriminative stimulus (DS) effect of apomorphine was investigated in rats trained in a two-lever, food-reinforcement procedure. Rats were given subcutaneous injections of saline or 0.1 mg/kg apomorphine HCl, 15 min before training sessions. The training dose of apomorphine was chosen to activate dopamine autoreceptors selectively. Stimulus generalization studies demonstrated that the DS effects generalized completely to other direct-acting dopaminergic agonists such as N-n-propylnorapomorphine (NPNA), pergolide, lergotrile, and bromocriptine. The indirect-acting dopamine agonists, (+)amphetamine, cocaine, and methylphenidate produced predominantly saline-appropriate lever responses. The DS effect of apomorphine at the training dose was incompletely antagonized by haloperidol or metoclopramide. The dopaminergic antagonists tested, however, also partially generalized to apomorphine. Both enantiomers of 3-(3-hydroxyphenyl)-N-n-propylpiperidine (3-PPP) produced apomorphine-appropriate lever choice with the (-) enantiomer being slightly more potent. The discriminative property of this (0.1 mg/kg) dose of apomorphine has characteristics consistent with selective dopamine autoreceptor activation.

摘要

在经过双杠杆食物强化程序训练的大鼠中研究了阿扑吗啡的辨别性刺激(DS)效应。在训练前15分钟,给大鼠皮下注射生理盐水或0.1mg/kg盐酸阿扑吗啡。选择阿扑吗啡的训练剂量以选择性激活多巴胺自身受体。刺激泛化研究表明,DS效应完全泛化到其他直接作用的多巴胺能激动剂,如N-正丙基去甲阿扑吗啡(NPNA)、培高利特、麦角腈和溴隐亭。间接作用的多巴胺激动剂,(+)苯丙胺、可卡因和哌醋甲酯主要产生与生理盐水相应的杠杆反应。训练剂量的阿扑吗啡的DS效应被氟哌啶醇或甲氧氯普胺不完全拮抗。然而,所测试的多巴胺能拮抗剂也部分泛化到阿扑吗啡。3-(3-羟基苯基)-N-正丙基哌啶(3-PPP)的两种对映体都产生了与阿扑吗啡相应的杠杆选择,其中(-)对映体的效力略强。这种(0.1mg/kg)剂量的阿扑吗啡的辨别特性具有与选择性多巴胺自身受体激活一致的特征。

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