Suppr超能文献

组胺H3受体与胃肠功能的最新进展

An update on histamine H3 receptors and gastrointestinal functions.

作者信息

Bertaccini G, Coruzzi G

机构信息

Institute of Pharmacology, University of Parma, Italy.

出版信息

Dig Dis Sci. 1995 Sep;40(9):2052-63. doi: 10.1007/BF02208678.

Abstract

The distribution and functions of histamine H3 receptors in the gastrointestinal tract is reviewed with particular reference to the effects on gastric acid secretion, mucosal protection, and intestinal motility. Histamine H3 receptor activation has negative effects on acid secretion induced by indirect secretagogues in cats, dogs, and rabbits; less clear effects were found in rats. An inhibitory effect on histamine release induced by different stimuli was observed in rats, rabbits, and dogs after H3 receptor agonists, thus supporting the idea that H3 receptors occur in ECL cells. (R)-alpha-methylhistamine has a marked protective effect against gastric lesions induced by ethanol in rats, being slightly less effective against aspirin and stress. H3 receptor activation decreases the intestinal motility induced by electrical stimulation in a variety of gut preparations, reducing both cholinergic and NANC neurotransmitter release. In this tissue the inhibitory effects mediated by histamine H3 receptors seem to be coupled, via a G protein, to a restriction of Ca2+ access into the nerve terminal; other mechanisms, however, have been suggested in the gastric mucosa. Histamine H3 receptors have already been subdivided into two receptor subtypes, H3A and H3B, the former being the subtype predominant in the gastrointestinal tissue. The increasing availability of selective agonists and antagonists of H3 receptors will unravel possible novel actions and physiological roles of histamine.

摘要

本文综述了组胺H3受体在胃肠道中的分布和功能,特别提及了其对胃酸分泌、黏膜保护和肠道运动的影响。组胺H3受体激活对猫、狗和兔子中间接促分泌剂诱导的胃酸分泌有负面影响;在大鼠中发现的影响不太明确。在给予H3受体激动剂后,在大鼠、兔子和狗中观察到对不同刺激诱导的组胺释放有抑制作用,从而支持了H3受体存在于肠嗜铬样(ECL)细胞中的观点。(R)-α-甲基组胺对大鼠乙醇诱导的胃损伤有显著保护作用,对阿司匹林和应激诱导的胃损伤的保护作用稍弱。H3受体激活降低了多种肠道制剂中电刺激诱导的肠道运动,减少了胆碱能和非肾上腺素能非胆碱能(NANC)神经递质的释放。在该组织中,组胺H3受体介导的抑制作用似乎通过G蛋白与限制Ca2+进入神经末梢相关联;然而,在胃黏膜中也提出了其他机制。组胺H3受体已被细分为两种受体亚型,H3A和H3B,前者是胃肠道组织中的主要亚型。H3受体选择性激动剂和拮抗剂的日益增多将揭示组胺可能的新作用和生理功能。

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