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Role of nociceptin/orphanin FQ and nociceptin opioid peptide receptor in depression and antidepressant effects of nociceptin opioid peptide receptor antagonists

机译:Nociceptin / orphanin FQ和nociceptin阿片肽受体在nociceptin阿片肽受体拮抗剂的抑郁和抗抑郁作用中的作用

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Nociceptin/orphanin FQ (N/OFQ) and its receptor, nociceptin opioid peptide (NOP) receptor, are localized in brain areas implicated in depression including the amygdala, bed nucleus of the stria terminalis, habenula, and monoaminergic nuclei in the brain stem. N/OFQ inhibits neuronal excitability of monoaminergic neurons and monoamine release from their terminals by activation of G protein-coupled inwardly rectifying Ksup+/sup channels and inhibition of voltage sensitive calcium channels, respectively. Therefore, NOP receptor antagonists have been proposed as a potential antidepressant. Indeed, mounting evidence shows that NOP receptor antagonists have antidepressant-like effects in various preclinical animal models of depression, and recent clinical studies again confirmed the idea that blockade of NOP receptor signaling could provide a novel strategy for the treatment of depression. In this review, we describe the pharmacological effects of N/OFQ in relation to depression and explore the possible mechanism of NOP receptor antagonists as potential antidepressants.
机译:Nociceptin / orphanin FQ(N / OFQ)及其受体,nociceptin阿片类肽(NOP)受体位于与抑郁症有关的大脑区域,包括杏仁核,终末纹的床核,哈贝努拉和脑干中的单胺能核。 N / OFQ分别通过激活G蛋白偶联的内向整流K + 通道和抑制电压敏感性钙通道来抑制单胺能神经元的神经元兴奋性和单胺从其末端释放。因此,已经提出了NOP受体拮抗剂作为潜在的抗抑郁药。实际上,越来越多的证据表明,NOP受体拮抗剂在各种临床前抑郁症动物模型中均具有抗抑郁样作用,最近的临床研究再次证实了NOP受体信号传导的阻断可以为抑郁症的治疗提供新策略的想法。在这篇综述中,我们描述了N / OFQ与抑郁症相关的药理作用,并探讨了NOP受体拮抗剂作为潜在抗抑郁药的可能机制。

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