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D1和D2拮抗剂对阿扑吗啡诱导的腹侧苍白球神经元反应的影响。

Effects of D1 and D2 antagonists on apomorphine-induced responses of ventral pallidal neurons.

作者信息

Maslowski R J, Napier T C

机构信息

Department of Pharmacology and Experimental Therapeutics, Loyola University Chicago, Stritch School of Medicine, Maywood, IL 60153.

出版信息

Neuroreport. 1991 Aug;2(8):451-4. doi: 10.1097/00001756-199108000-00010.

Abstract

The ventral pallidum with the adjacent substantia innominata (VP) has been described as a dopaminoceptive brain region. Repeated systemic injections of the dopamine agonist, apomorphine, induce dose-dependent alterations in VP neuronal activity. The present studies evaluated the contribution of D1 and D2 receptor subtypes to apomorphine-induced alterations in extracellularly recorded VP neuronal activity. Both sulpiride (D2 antagonist) and SCH23390 (D1 antagonist) attenuated many of these responses; however, pretreatment with either antagonist did not alter the number of responding neurons, or the maximal effect induced by apomorphine. Thus, activation of either receptor subtype by apomorphine is sufficient to initiate the observed responses, and both may be involved in dopaminergic modulation of VP neurons.

摘要

腹侧苍白球及其相邻的无名质(VP)被描述为一个多巴胺感受性脑区。重复全身性注射多巴胺激动剂阿扑吗啡会诱导VP神经元活动出现剂量依赖性改变。本研究评估了D1和D2受体亚型对阿扑吗啡诱导的细胞外记录的VP神经元活动改变的作用。舒必利(D2拮抗剂)和SCH23390(D1拮抗剂)均减弱了许多此类反应;然而,用任何一种拮抗剂预处理均未改变反应神经元的数量,或阿扑吗啡诱导的最大效应。因此,阿扑吗啡对任一受体亚型的激活足以引发观察到的反应,且两者可能都参与了VP神经元的多巴胺能调节。

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