Functional blockade of opioid analgesia by orphanin FQ/nociceptin

被引:46
作者
King, M [1 ]
Chang, A [1 ]
Pasternak, GW [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Neurol, Cotzias Lab Neurooncol, New York, NY 10021 USA
关键词
morphine; opioid receptor; KOR-3; analgesia; anti-opioid;
D O I
10.1016/S0006-2952(98)00023-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Orphanin FQ/nociceptin (OFQ/N) is a recently identified neuropeptide with high affinity for the orphan opioid receptor. OFQ/N blocked morphine analgesia in mice in a dose-dependent manner, as well as the analgesic actions of [D-Pen(2), D-Pen(5)]enkephalin (DPDPE), morphine-6 beta-glucuronide, trans-3,4-dichloro-N-[2(1-pyrrolindinyl)-cyclohexyl]-benzeneacetamide methane sulfonate hydrate (U50,488H) and naloxone benzoylhydrazone. These actions are anti-analgesic, because OFQ/N also blocked clonidine analgesia and OFQ/N was inactive against the inhibition of gastrointestinal transit by morphine. Although OFQ/N was quite potent in these paradigms, two truncated forms, OFQ/N(1-11) and OFQ/N(1-7), were inactive. An antisense oligodeoxynucleotide targeting the first coding exon of KOR-3, the mouse homolog of the orphan opioid receptor, effectively prevented the anti-opioid actions of OFQ/N, confirming the importance of the orphan opioid receptor in this action. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:1537 / 1540
页数:4
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