Stress-induced analgesia in μ-apioid receptor knockout mice reveals normal function of the δ-opioid receptor system

被引:31
作者
LaBuda, CJ
Sora, I
Uhl, GR
Fuchs, PN
机构
[1] Univ Texas, Dept Psychol, Arlington, TX 76019 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol & Neurosci, Baltimore, MD 21224 USA
[3] NIDA, Intramural Res Program, Mol Neurobiol Branch, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
antinociception; morphine; opioid receptor; naltrindole; transgenic mouse; stress-induced analgesia;
D O I
10.1016/S0006-8993(00)02196-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stress-induced analgesia (SIA) was examined in wildtype and mu-opioid receptor knockout mice. We used thermal paw withdrawal (TPW) latency following a continuous 3-min swim in 20 degrees C water, and found a significant increase in TPW latency in both wild-type and knockout mice. Pre-treatment prior to the swim with naltrindole, a selective delta-opioid receptor antagonist, blocked the increase in TPW latency in knockout mice. These results demonstrate an intact delta-receptor-mediated function of a physiologically-released endogenous agonist in the mu-opioid receptor knockout mouse. The present findings are in contrast with previous reports that analgesia induced by exogenous delta agonists is reduced in the knockout mice. (C) 2000 Elsevier Science BN. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
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