Bidirectional modulatory effect of orphanin FQ on morphine-induced analgesia: Antagonism in brain and potentiation in spinal cord of the rat

被引:218
|
作者
Tian, JH
Xu, W
Fang, Y
Mogil, JS
Grisel, JE
Grandy, DK
Han, JS
机构
[1] BEIJING MED UNIV, CTR RES NEUROSCI, BEIJING 100083, PEOPLES R CHINA
[2] OREGON HLTH SCI UNIV, DEPT BEHAV NEUROSCI, PORTLAND, OR 97201 USA
[3] OREGON HLTH SCI UNIV, VOLLUM INST ADV BIOMED RES, PORTLAND, OR 97201 USA
关键词
analgesia; anti-opioid; ORL(1)/LC132; orphanin FQ nociceptin; morphine withdrawal;
D O I
10.1038/sj.bjp.0700942
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The present study was designed to investigate further the effects of the newly discovered orphanin FQ (OFQ) - the endogenous ligand for the orphan opioid receptor (called, e.g., ORL(1) and LC132) - on pain modulation in the rat. We used the tail-flick assay as a nociceptive index. 2 When injected into a cerebral ventricle, OFQ (4 fmol-10 nmol) has no effect on basal tail-flick latency by itself at any dose, but dose-dependently antagonizes systemic morphine analgesia (400 fmol-50 nmol). 3 Injected intrathecally, OFQ (3 and 10 nmol) displayed an analgesic effect without producing motor dysfunction, and potentiated morphine analgesia (1 and 10 nmol). 4 The anti-opioid effect of OFQ in rat brain and the high level of expression of LC132/ORL(1) receptor in the locus coeruleus indicated a possible role of OFQ in the precipitation of opiate withdrawal symptoms. However, no such precipitation was observed by OFQ in morphine-dependent rats.
引用
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页码:676 / 680
页数:5
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