Melatonin enhances antinociceptive effects of δ-, but not μ-opioid agonist in mice

被引:45
作者
Li, SR
Wang, T
Wang, R
Dai, X
Chen, Q
Li, RD
机构
[1] Lanzhou Univ, Sch Life Sci, Dept Biochem & Mol Biol, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
melatonin; opioid; deltorphin I; endomorphin-1; antinociception; mice;
D O I
10.1016/j.brainres.2005.02.067
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This present study examines the effect of melatonin on antinociceptive action induced by opioid agonists in mice using the tail-flick test. When injected either by intraperitoneal (i.p.) (1, 5, 25 mg/kg) or by intracerebroventricular (i.c.v.) (0.25, 0.5, 1 mg/kg) routes, melatonin significantly enhanced the delta-opioid agonist deltorphin I induced antinociception, but not mu-opioid agonist endomorphin-1. Further investigation showed that i.c.v. luzindole (0.5 mg/kg) (an antagonist of melatonin receptor) significantly antagonized the enhanced antinociceptive effect of i.c.v. melatonin. These results demonstrated that melatonin can specifically enhance the antinociception induced by specific opioid receptor agonist (i.e., delta opioid agonist) acting on melatonin receptor and that melatonin may have augmentation effect on analgesia with delta-, but not mu-opioid agonists in mice. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:132 / 138
页数:7
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