Suppr超能文献

组胺能药物对大鼠肠系膜微循环中肾上腺素能神经传递的原位效应。

In situ effects of histaminergic agents on adrenergic neurotransmission in rat mesenteric microcirculation.

作者信息

Todorov S, Janiec W, Sliwinski L, Folwarczna J

机构信息

Institute of Physiology, Bulgarian Academy of Sciences, Sofia, Bulgaria.

出版信息

Acta Physiol Pharmacol Bulg. 1989;15(2):13-7.

PMID:2552746
Abstract

Experiments were performed to study in situ the effects of histamine and some H1- or H2-agonists and antagonists on the contractions of the rat mesenteric methaarterioles (RMMA) induced by 0.6 nM noradrenaline (NA) applied locally or by electrical stimulation (ES). All drugs tested (cimetidine--300 nM, the others --30 nM) were also applied locally 30 s before the contractile stimulus. NA and ES strongly contracted the blood vessels. Of all drugs studied only diphenhydramine (DPH) evoked a slight contraction of RMMA. Histamine markedly inhibited the contractile responses to NA and ES. Similar effects were exerted by 2-(2-aminoethyl)thiazole (2-AET) its inhibitory action on the ES-induced contractions being weaker than that of histamine. Dimaprit (DMP) only tended to inhibit the RMMA contractions. DPH abolished the NA-induced contractions while cimetidine (CIM) did not change the effects of NA and ES. The results suggest that H1-receptors are mainly involved in the modifying action of histaminergic drugs on the adrenergic neurotransmission in RMMA.

摘要

进行实验以原位研究组胺及一些H1或H2激动剂和拮抗剂对局部应用0.6 nM去甲肾上腺素(NA)或电刺激(ES)诱导的大鼠肠系膜微动脉(RMMA)收缩的影响。所有测试药物(西咪替丁——300 nM,其他药物——30 nM)也在收缩刺激前30秒局部应用。NA和ES强烈收缩血管。在所有研究的药物中,只有苯海拉明(DPH)引起RMMA轻微收缩。组胺显著抑制对NA和ES的收缩反应。2-(2-氨基乙基)噻唑(2-AET)也有类似作用,其对ES诱导收缩的抑制作用比组胺弱。二甲双胍(DMP)仅倾向于抑制RMMA收缩。DPH消除了NA诱导的收缩,而西咪替丁(CIM)未改变NA和ES的作用。结果表明,H1受体主要参与组胺能药物对RMMA中肾上腺素能神经传递的调节作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验