Orphanin FQ/nociceptin: a role in pain and analgesia, but so much more

被引:254
作者
Darland, T [1 ]
Heinricher, MM
Grandy, DK
机构
[1] Oregon Hlth & Sci Univ, Dept Dev & Cell Biol, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Neurosurg, Portland, OR 97201 USA
[3] Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97201 USA
关键词
D O I
10.1016/S0166-2236(97)01204-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The publication of the delta opioid receptor sequence led to the cloning of three homologous receptors: the mu and kappa opioid receptors, and a novel opioid-like orphan receptor. The orphan receptor's endogenous ligand, a 17-amino-acid peptide that resembles dynorphin, was named 'orphanin FQ' and 'nociceptin' (OFQ/N1-17). The OFQ/N1-17 receptor is expressed widely in the nervous system, and it is becoming clear that the peptide is likely to participate in a broad range of physiological and behavioral functions. At the cellular level, OFQ/N1-17 has much in common with the classical opioids; however, functional studies are now revealing distinct actions of this peptide Identified only two years ago, QFQ/N1-17 has already attracted a great deal of attention. The number and diversity of papers focused on OFQ/N1-17 at the recent meeting of the Society for Neuroscience augur an exciting future for this new peptide.
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页码:215 / 221
页数:7
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