Nociceptin inhibits tonic nitric oxide release in the mouse isolated proximal colon

被引:15
|
作者
Menzies, JRW [1 ]
Corbett, AD [1 ]
机构
[1] Glasgow Caledonian Univ, Sch Biol & Biomed Sci, Glasgow G4 0BA, Lanark, Scotland
关键词
nociceptin; ORL1; receptor; colon; mouse; isolated; nitric oxide (NO);
D O I
10.1016/S0014-2999(99)00858-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nociceptin/orphanin FQ, the endogenous ligand of the opioid receptor-like (ORL1) receptor, caused contractions in the isolated colon of the mouse. Tetrodotoxin and the nitric oxide (NO) synthase inhibitor N omega-nitro-L-arginine also produced contractions which were quantitatively similar to those seen in response to nociceptin. In the presence of either tetrodotoxin or N omega-nitro-L-arginine, nociceptin was unable to cause a further contraction, whereas the muscarinic receptor agonist carbachol elicited a contractile response. Nociceptin had no contractile activity in colonic preparations contracted by No-nitro-L-arginine then relaxed by addition of the NO donor sodium nitroprusside. These data suggest that nociceptin causes contractions of the mouse proximal colon by inhibiting the tonic, neuronal release of NO. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:183 / 186
页数:4
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