Suppr超能文献

5-羟色胺4受体是否介导大鼠体内5-羟色胺引起的肠道分泌反应?

Do 5-HT4 receptors mediate the intestinal secretory response to 5-HT in rat in-vivo?

作者信息

Franks C M, Hardcastle J, Hardcastle P T, Sanger G J

机构信息

Department of Biomedical Science, University of Sheffield, UK.

出版信息

J Pharm Pharmacol. 1995 Mar;47(3):213-8. doi: 10.1111/j.2042-7158.1995.tb05781.x.

Abstract

The involvement of the recently characterized 5-HT4 receptor in the actions of 5-hydroxytryptamine (5-HT) on jejunal, ileal and colonic electrogenic ion secretion was investigated in the rat in-vivo. 5-HT and the 5-HT1-, 5-HT2- and 5-HT4-receptor agonist 5-methoxytryptamine (5-MeOT), induced a rise in transintestinal PD in all regions of the gut. However, the 5-HT4-receptor agonists renzapride and cisapride had no effect. Furthermore, the 5-HT4-receptor antagonists SDZ 205-557 (2-diethylaminoethyl-[2-methoxy-4-amino-5-chloro] benzoate), tropisetron and SB 204070 ([1-butyl-4-piperidinylmethyl]-8-amino-7-chloro-1,4- benzodioxan-5-carboxylate hydrochloride) did not affect the secretory response to either 5-HT or 5-MeOT in the jejunum, but did cause a small inhibition in the ileum and colon. It is concluded that 5-HT4 receptors do not make a contribution to the electrically monitored 5-HT intestinal secretory response in the rat jejunum in-vivo, but may play a small role in the ileum and colon.

摘要

在大鼠体内研究了最近鉴定的5-羟色胺4(5-HT4)受体在5-羟色胺(5-HT)对空肠、回肠和结肠电生性离子分泌作用中的参与情况。5-HT以及5-HT1、5-HT2和5-HT4受体激动剂5-甲氧基色胺(5-MeOT)在肠道所有区域均引起跨肠电位差升高。然而,5-HT4受体激动剂renzapride和西沙必利没有作用。此外,5-HT4受体拮抗剂SDZ 205-557(2-二乙氨基乙基-[2-甲氧基-4-氨基-5-氯]苯甲酸酯)、托烷司琼和SB 204070([1-丁基-4-哌啶基甲基]-8-氨基-7-氯-1,4-苯并二恶烷-5-羧酸盐酸盐)对空肠中5-HT或5-MeOT的分泌反应没有影响,但在回肠和结肠中确实引起了轻微抑制。得出的结论是,5-HT4受体对大鼠体内空肠中电监测的5-HT肠道分泌反应没有贡献,但可能在回肠和结肠中起较小作用。

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