Orphanin FQ is a functional anti-opioid peptide

被引:347
作者
Mogil, JS
Grisel, JE
Reinscheid, RK
Civelli, O
Belknap, JK
Grandy, DK
机构
[1] OREGON HLTH SCI UNIV, VOLLUM INST ADV BIOMED RES, PORTLAND, OR 97201 USA
[2] VET ADM MED CTR, RES SERV, PORTLAND, OR 97201 USA
[3] OREGON HLTH SCI UNIV, DEPT BEHAV NEUROSCI, PORTLAND, OR 97201 USA
[4] F HOFFMANN LA ROCHE & CO LTD, DIV PHARMA, CNS RES, CH-4002 BASEL, SWITZERLAND
关键词
orphanin FQ; LC132; nociception; anti-opioid; morphine; mice;
D O I
10.1016/0306-4522(96)00338-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The heptadecapeptide orphanin FQ has recently been shown to be the endogenous agonist for the orphan opioid-like receptor, LC132. The molecular evidence that LC132 and orphanin FQ are evolutionarily related to other opioid receptors and their ligands suggests that these proteins may also play a role in modulating opiate actions. We now report that orphanin FQ (0.5 - 10 nmol), injected intracerebroventricularly in mice, does not produce hyperalgesia as suggested previously but rather reverses opioid-mediated (i.e. naloxone-sensitive) stress-induced antinociception in three different algesiometric assays. In addition to its antagonism of endogenous opioid antinociception, orphanin FQ dose-dependently (2.5 - 25 nmol) reverses systemic morphine antinociception (5 mg/kg, s.c.). Based on these data, we propose that orphanin FQ is a functional anti-opioid peptide. Copyright (C) 1996 IBRO.
引用
收藏
页码:333 / 337
页数:5
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