Nociceptin/orphanin FQ and neurotransmitter release in the central nervous system

被引:118
|
作者
Schlicker, E
Morari, M
机构
[1] Univ Bonn, Dept Pharmacol & Toxicol, D-53113 Bonn, Germany
[2] Univ Ferrara, Pharmacol Sect, Dept Expt & Cli Med, I-44100 Ferrara, Italy
关键词
acetylcholine; glutamate; 5-hydroxytryptamine (serotonin; 5-HT); naloxone benzoylhydrazone; nociceptin; noradrenaline; Nphe(1)]nociceptin-(1-13)NH2; orphanin FQ; Phe(1)psi(CH2-NH)Gly(2)]nociceptin(1-13)NH2;
D O I
10.1016/S0196-9781(00)00233-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this article, the effect of nociceptin (orphanin FQ) on transmitter release in the central nervous system in vitro and in vivo is reviewed. Nociceptin inhibits the electrically or K+-evoked noradrenaline, dopamine, serotonin, and glutamate release in brain slices from guinea-pig, rat, and mouse. This effect is usually naloxone-resistant but antagonized by OF, receptor antagonists like [Phe(1)psi(CH2-NH)Gly(2)]-nociceptin(1-13)NH2. In the rat in vivo, nociceptin diminishes acetylcholine release in the striatum: reduces dopamine release, and prevents the stimulatory effect of morphine on this transmitter in the nucleus accumbens and also elevates extracellular glutamate and gamma-aminobutyric acid levels in mesencephalic dopaminergic areas. The effect of nociceptin on the mesencephalic dopaminergic system might explain its actions on motor behavior. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1023 / 1029
页数:7
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