Gavioli Elaine C, Holanda Victor A D, Ruzza Chiara
Behavioral Pharmacology Laboratory, Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, Brazil.
Department of Medical Sciences, Section of Pharmacology, and National Institute of Neuroscience, University of Ferrara, Ferrara, Italy.
Handb Exp Pharmacol. 2019;254:233-257. doi: 10.1007/164_2018_188.
Many studies point toward the nociceptin/orphanin FQ (N/OFQ) and the N/OFQ peptide receptor (NOP) as targets for the development of innovative drugs for treating anxiety- and mood-related disorders. Evidence supports the view that the activation of NOP receptors with agonists elicits anxiolytic-like effects, while its blockade with NOP antagonists promotes antidepressant-like actions in rodents. Genetic studies showed that NOP receptor knockout mice display an antidepressant-like phenotype, and NOP antagonists are inactive in these animals. In contrast, the genetic blockade of NOP receptor signaling generally displays an increase of anxiety states in the elevated plus-maze test. In this chapter we summarized the most relevant findings of NOP receptor ligands in the modulation of anxiety and mood disorders, and the putative mechanisms of action are discussed.
许多研究表明,孤啡肽/孤啡肽FQ(N/OFQ)和N/OFQ肽受体(NOP)可作为开发治疗焦虑和情绪相关障碍创新药物的靶点。有证据支持这样的观点,即激动剂激活NOP受体会引发抗焦虑样效应,而用NOP拮抗剂阻断该受体则会在啮齿动物中促进抗抑郁样作用。基因研究表明,NOP受体基因敲除小鼠表现出抗抑郁样表型,且NOP拮抗剂在这些动物中无活性。相反,在高架十字迷宫试验中,NOP受体信号的基因阻断通常会导致焦虑状态增加。在本章中,我们总结了NOP受体配体在调节焦虑和情绪障碍方面最相关的研究结果,并讨论了其可能的作用机制。