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大鼠心脏副交感神经支配中多巴胺受体的药理学特性

Pharmacological characterization of dopamine receptors in parasympathetic innervation of rat heart.

作者信息

Roquebert J, Moran A, Demichel P, Sauvage M F

机构信息

Laboratoire de Pharmacodynamie, U.F.R. de Pharmacie, Université de Bordeaux, France.

出版信息

Eur J Pharmacol. 1991 Jul 23;200(1):59-63. doi: 10.1016/0014-2999(91)90665-d.

Abstract

The action of dopamine agonists (apomorphine, bromocriptine, pergolide and quinpirole) on the bradycardia induced in vivo by electrical stimulation of the vagus nerves was studied in pithed rats pretreated with atenolol. The dopamine agonists decreased significantly the vagal-induced but not the acetylcholine-induced bradycardia. The first effect was blocked by (S)-sulpiride or domperidone but not by yohimbine, prazosin or SCH 23390. Both effects were antagonized by methylatropine. The data suggest the presence of presynaptic and/or ganglionic dopamine DA2 receptors in the parasympathetic innervation of the rat heart, stimulation of which inhibits the release of acetylcholine.

摘要

在预先用阿替洛尔处理的去大脑大鼠中,研究了多巴胺激动剂(阿扑吗啡、溴隐亭、培高利特和喹吡罗)对迷走神经电刺激在体内诱发的心动过缓的作用。多巴胺激动剂显著降低了迷走神经诱发的心动过缓,但对乙酰胆碱诱发的心动过缓没有影响。第一种作用被(S)-舒必利或多潘立酮阻断,但未被育亨宾、哌唑嗪或SCH 23390阻断。两种作用均被甲基阿托品拮抗。数据表明,在大鼠心脏的副交感神经支配中存在突触前和/或神经节多巴胺DA2受体,刺激这些受体可抑制乙酰胆碱的释放。

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