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苯丙胺对大鼠自我刺激的作用及相互作用。

Actions and interactions of amphetamine on self-stimulation in rats.

作者信息

Aulakh C S, Pradhan S N

出版信息

Pharmacol Biochem Behav. 1979 Sep;11(3):351-4. doi: 10.1016/0091-3057(79)90148-5.

Abstract

The dose-response relationship for d-amphetamine (0.125-2 mg/kg, IP) and its l-isomer (0.125-3 mg/kg, IP) was studied in self-stimulation behavior of rats each with an electrode at posterior hypothalamus (PH, mainly monoaminergic) or area ventralis tegmentum (A10, dopaminergic). The drug effects increased with the dose reaching a peak (at 0.5 mg/kg with d-amphetamine and at 1.0 mg/kg with 1-amphetamine) and then decreased. The d-isomer was approximately twice as potent as the l-isomer in enhancing intracranial self-stimulation (ICSS) rate with electrodes at either site. Azaperone (mainly an alpha-adrenergic blocker) and haloperidol (an antidopaminergic neuroleptic) used in small doses (0.05 and 0.008 mg/kg respectively) which did not affect the baseline responding, blocked amphetamine-induced enhancement of ICSS in both groups of rats. Thus, amphetamine-induced facilitation of ICSS at both PH and A10 areas and its blockade by an alpha-adrenergic blocker as well as an antidopaminergic neuroleptic show the involvement of both noradrenergic and dopaminergic mechanisms in self-stimulation behavior.

摘要

研究了右旋苯丙胺(0.125 - 2毫克/千克,腹腔注射)及其左旋异构体(0.125 - 3毫克/千克,腹腔注射)对大鼠自我刺激行为的剂量 - 反应关系,每只大鼠在下丘脑后部(PH,主要为单胺能)或腹侧被盖区(A10,多巴胺能)植入电极。药物效应随剂量增加达到峰值(右旋苯丙胺为0.5毫克/千克,左旋苯丙胺为1.0毫克/千克),然后下降。在两个部位植入电极时,右旋异构体增强颅内自我刺激(ICSS)率的效力约为左旋异构体的两倍。小剂量使用的阿扎哌隆(主要为α - 肾上腺素能阻滞剂)和氟哌啶醇(抗多巴胺能神经阻滞剂)(分别为0.05和0.008毫克/千克)不影响基线反应,但能阻断两组大鼠中苯丙胺诱导的ICSS增强。因此,苯丙胺在PH和A10区域诱导的ICSS促进作用及其被α - 肾上腺素能阻滞剂和抗多巴胺能神经阻滞剂阻断,表明去甲肾上腺素能和多巴胺能机制均参与自我刺激行为。

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