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孤儿阿片受体反义探针可阻断孤啡肽诱导的摄食过量。

Orphan opioid receptor antisense probes block orphanin FQ-induced hyperphagia.

作者信息

Leventhal L, Mathis J P, Rossi G C, Pasternak G W, Bodnar R J

机构信息

Department of Psychology, Queens College, City University of New York, Flushing 11367, USA.

出版信息

Eur J Pharmacol. 1998 May 15;349(1):R1-3. doi: 10.1016/s0014-2999(98)00272-6.

Abstract

Orphanin FQ/nociceptin binds with high affinity to the orphan opioid receptor-like/K-3 (ORL1/KOR-3) clone, and stimulates feeding. The present study demonstrated that antisense oligodeoxynucleotides directed against either exons 1, 2 or 3 of the ORL1/KOR-3 clone reduced orphanin FQ/nociceptin-induced hyperphagia. A missense probe was ineffective. Naltrexone dose-dependently reduced orphanin FQ/nociceptin-induced hyperphagia. These data suggest that the receptor responsible for orphanin FQ/nociceptin-induced hyperphagia is encoded by the ORL1/KOR-3 clone.

摘要

孤啡肽/痛敏肽与孤儿阿片样受体样/K-3(ORL1/KOR-3)克隆体具有高亲和力结合,并刺激进食。本研究表明,针对ORL1/KOR-3克隆体的外显子1、2或3的反义寡脱氧核苷酸可减少孤啡肽/痛敏肽诱导的摄食过量。错义探针无效。纳曲酮剂量依赖性地减少孤啡肽/痛敏肽诱导的摄食过量。这些数据表明,负责孤啡肽/痛敏肽诱导摄食过量的受体由ORL1/KOR-3克隆体编码。

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