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μ-阿片受体基因敲除小鼠:μ-阿片受体在胃肠转运中的作用

mu-Opioid receptor-knockout mice: the role of mu-opioid receptor in gastrointestinal transit.

作者信息

Roy S, Liu H C, Loh H H

机构信息

Department of Pharmacology, University of Minnesota Medical School, Minneapolis, MN 55455, USA.

出版信息

Brain Res Mol Brain Res. 1998 May;56(1-2):281-3. doi: 10.1016/s0169-328x(98)00051-5.

Abstract

The role of mu-opioid receptor in gastrointestinal transit was investigated using mu-opioid receptor knockout mice (MOR-KO). Our result establishes unequivocally that inhibition of GI transit by morphine is a mu-opioid receptor mediated function. In addition, we show that neither delta nor kappa receptor agonist given supraspinally or peripherally are able to inhibit GI transit in MOR-KO animals. It was interesting to observe that basal GI motility was lower in MOR-KO (-/-) compared to heterozygous (+/-) and wild type (+/+) animals.

摘要

利用μ-阿片受体基因敲除小鼠(MOR-KO)研究了μ-阿片受体在胃肠转运中的作用。我们的结果明确证实,吗啡对胃肠转运的抑制是一种由μ-阿片受体介导的功能。此外,我们还表明,无论是脊髓上还是外周给予δ或κ受体激动剂,均无法抑制MOR-KO动物的胃肠转运。有趣的是,观察到与杂合子(+/-)和野生型(+/+)动物相比,MOR-KO(-/-)动物的基础胃肠动力较低。

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