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腹侧纹状体中乙酰胆碱的释放受组胺受体的影响。

Release of acetylcholine in the ventral striatum is influenced by histamine receptors.

作者信息

Prast H, Fischer H, Philippu A

机构信息

Department of Pharmacology and Toxicology, University of Innsbruck, Austria.

出版信息

Agents Actions. 1994 Jun;41 Spec No:C85-6. doi: 10.1007/BF02007778.

Abstract

To investigate whether histamine receptor ligands influence the in vivo-release of acetylcholine in the ventral striatum, this brain region was superfused with histamine receptor agonists or antagonists through a push-pull cannula and drug effects on the release of acetylcholine were investigated. Histamine, the H1 receptor agonist 2-thiazolyl-ethylamine and the H3 receptor antagonist thioperamide enhanced acetylcholine release, while the H3 receptor agonist (R)-alpha-methylhistamine was ineffective. The results indicate that H1 receptors and H3 receptors modulate acetylcholine release. The thioperamide-induced increase of acetylcholine release might be exerted via H3-receptors located on cholinergic terminals. Alternatively, thioperamide might enhance acetylcholine release by increasing endogenous histamine release via H3 autoreceptors. It is concluded that, via stimulation of striatal H1- and H3 receptors, histaminergic neurons are involved in the regulation of cholinergic neuronal activity in the ventral striatum.

摘要

为了研究组胺受体配体是否会影响腹侧纹状体中乙酰胆碱的体内释放,通过推挽式套管向该脑区灌注组胺受体激动剂或拮抗剂,并研究药物对乙酰胆碱释放的影响。组胺、H1受体激动剂2-噻唑基乙胺和H3受体拮抗剂硫代哌啶增强了乙酰胆碱的释放,而H3受体激动剂(R)-α-甲基组胺则无效。结果表明,H1受体和H3受体调节乙酰胆碱的释放。硫代哌啶诱导的乙酰胆碱释放增加可能是通过位于胆碱能终末的H3受体发挥作用。或者,硫代哌啶可能通过H3自身受体增加内源性组胺释放来增强乙酰胆碱的释放。得出的结论是,通过刺激纹状体H1和H3受体,组胺能神经元参与腹侧纹状体中胆碱能神经元活动的调节。

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