Involvements of mu- and kappa-opioid receptors in morphine-induced antinociception in the nucleus accumbens of rats

被引:15
作者
Xiong, Wei
Yu, Long-Chuan [1 ]
机构
[1] Peking Univ, Coll Life Sci, Neurobiol Lab, Beijing 100871, Peoples R China
[2] Peking Univ, Coll Life Sci, Natl Lab Biomembrane & Membrane Biotechnol, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
antinociception; nucleus accumbens; morphine; opioid receptor; hindpaw withdrawal latency;
D O I
10.1016/j.neulet.2006.01.052
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It is well known that there are three types of opioid receptors, mu- (MOR), delta- (DOR), and kappa-opioid receptor (KOR) in the central nervous system. The present study investigated the involvement of opioid receptors in morphine-induced antinociception in the nucleus accumbens (NAc) of rats. The hindpaw withdrawal latencies to thermal and mechanical stimulation increased markedly after intra-NAc administration of morphine. The antinociceptive effects induced by morphine were dose-dependently inhibited by intra-NAc administration of the non-selective opioid receptor antagonist naloxone. Furthermore, the morphine-induced antinociception was significantly attenuated by subsequent intra-NAc injection of the MOR antagonist beta-funaltrexamine or the KOR antagonist nor-binaltorphimine, but not the DOR antagonist naltrindole. The results indicate that MOR and KOR, but not DOR are involved in the morphine-induced antinociception in the NAc of rats. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:167 / 170
页数:4
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