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The molecular and behavioral pharmacology of the orphanin FQociceptin peptide and receptor family.

机译:orphanin FQ / nociceptin肽和受体家族的分子和行为药理学。

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摘要

The isolation of an opioid receptor-related clone soon led to the isolation and characterization of a new neuropeptide, termed orphanin FQ or nociceptin (OFQ/N). This heptadecapeptide binds to the NOP(1) (previously termed ORL1) receptor with exceedingly high affinity, but does not interact directly with classical opioid receptors. Functionally, the actions of OFQ/N are diverse and intriguing. Most work has focused upon pain mechanisms, where OFQ/N has potent anti-analgesic actions supraspinally and analgesic actions spinally. Other OFQ/N activities are less clear. The diversity of responses might reflect NOP(1) receptor heterogeneity, but this remains to be established. The actions of this neurochemical system may also be uniquely dependent on contextual factors, both genetic and environmental. This review will address the molecular biology and behavioral pharmacology of OFQ/N and its receptor.
机译:阿片受体相关克隆的分离很快导致了一种新的神经肽的分离和鉴定,这种神经肽称为孤儿蛋白FQ或伤害感受蛋白(OFQ / N)。该七肽以极高的亲和力与NOP(1)(以前称为ORL1)受体结合,但不直接与经典阿片受体相互作用。在功能上,OFQ / N的动作是多样且有趣的。大多数工作都集中在疼痛机制上,其中OFQ / N在脊髓上方具有有效的止痛作用,在脊髓上具有有效的止痛作用。其他OFQ / N活动不太清楚。反应的多样性可能反映了NOP(1)受体的异质性,但这仍有待确定。这个神经化学系统的作用也可能唯一地取决于遗传和环境的背景因素。这篇综述将探讨OFQ / N及其受体的分子生物学和行为药理学。

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