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2
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Nociceptin/Orphanin FQ Receptor Structure, Signaling, Ligands, Functions, and Interactions with Opioid Systems.孤啡肽/痛敏肽受体的结构、信号传导、配体、功能以及与阿片系统的相互作用
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Pharmacological characterization of nociceptin/orphanin FQ receptors, a novel opioid receptor family, in the midbrain periaqueductal gray.中脑导水管周围灰质中新型阿片受体家族——孤啡肽受体的药理学特性
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本文引用的文献

1
Blockade of nociceptin/orphanin FQ signaling facilitates an active copying strategy due to acute and repeated stressful stimuli in mice.由于急性和反复的应激刺激,在小鼠中阻断痛敏肽/孤啡肽FQ信号传导有助于一种主动应对策略。
Neurobiol Stress. 2020 Oct 5;13:100255. doi: 10.1016/j.ynstr.2020.100255. eCollection 2020 Nov.
2
Differential Modulation of Ventral Tegmental Area Circuits by the Nociceptin/Orphanin FQ System.孤啡肽/强啡肽系统对腹侧被盖区回路的差异调节。
eNeuro. 2020 Oct 19;7(5). doi: 10.1523/ENEURO.0376-19.2020. Print 2020 Jul/Aug.
3
Fear expression is reduced after acute and repeated nociceptin/orphanin FQ (NOP) receptor antagonism in rats: therapeutic implications for traumatic stress exposure.急性和反复的孤啡肽/N 端前脑啡肽原(NOP)受体拮抗剂可减少大鼠的恐惧表达:创伤性应激暴露的治疗意义。
Psychopharmacology (Berl). 2020 Oct;237(10):2943-2958. doi: 10.1007/s00213-020-05582-0. Epub 2020 Jun 25.
4
The Rewarding and Anxiolytic Properties of Ethanol within the Central Nucleus of the Amygdala: Mediated by Genetic Background and Nociceptin.杏仁中央核内乙醇的奖赏和抗焦虑特性:由遗传背景和孤啡肽介导。
J Pharmacol Exp Ther. 2020 Sep;374(3):366-375. doi: 10.1124/jpet.119.262097. Epub 2020 Jun 11.
5
Effects of Cebranopadol on Cocaine-induced Hyperactivity and Cocaine Pharmacokinetics in Rats.塞布若啡对可卡因诱导的大鼠多动和可卡因药代动力学的影响。
Sci Rep. 2020 Jun 9;10(1):9254. doi: 10.1038/s41598-020-66250-z.
6
NOP receptor agonist attenuates nitroglycerin-induced migraine-like symptoms in mice.NOP 受体激动剂可减轻小鼠硝化甘油诱导的偏头痛样症状。
Neuropharmacology. 2020 Jun 15;170:108029. doi: 10.1016/j.neuropharm.2020.108029. Epub 2020 Mar 6.
7
Blockade of NOP receptor modulates anxiety-related behaviors in mice exposed to inescapable stress.阻断 NOP 受体可调节暴露于不可逃避应激的小鼠的焦虑相关行为。
Psychopharmacology (Berl). 2020 Jun;237(6):1633-1642. doi: 10.1007/s00213-020-05487-y. Epub 2020 Feb 24.
8
Potent and selective NOP receptor activation reduces cocaine self-administration in rats by lowering hedonic set point.强效且选择性的 NOP 受体激活通过降低愉悦设定点来减少大鼠的可卡因自我给药。
Addict Biol. 2020 Nov;25(6):e12844. doi: 10.1111/adb.12844. Epub 2019 Nov 10.
9
NOP Receptor Antagonists Decrease Alcohol Drinking in the Dark in C57BL/6J Mice.NOP 受体拮抗剂可减少 C57BL/6J 小鼠在黑暗中的饮酒行为。
Alcohol Clin Exp Res. 2019 Oct;43(10):2167-2178. doi: 10.1111/acer.14165. Epub 2019 Aug 21.
10
A Paranigral VTA Nociceptin Circuit that Constrains Motivation for Reward.一个位于中脑腹侧被盖区的旁巨细胞核伤害感受神经元回路,它限制了对奖赏的动机。
Cell. 2019 Jul 25;178(3):653-671.e19. doi: 10.1016/j.cell.2019.06.034.

神经精神疾病中的 NOP 受体系统:在开发靶向治疗方法中的差异、特点和临床进展。

The NOP Receptor System in Neurological and Psychiatric Disorders: Discrepancies, Peculiarities and Clinical Progress in Developing Targeted Therapies.

机构信息

Department of Biomedical Sciences, Charles E. Schmidt College of Medicine, Florida Atlantic University, 777 Glades Rd, Boca Raton, FL, 33431, USA.

出版信息

CNS Drugs. 2021 Jun;35(6):591-607. doi: 10.1007/s40263-021-00821-0. Epub 2021 May 31.

DOI:10.1007/s40263-021-00821-0
PMID:34057709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8279133/
Abstract

The nociceptin opioid peptide (NOP) receptor and its endogenous ligand nociceptin/orphanin FQ (N/OFQ) are the fourth members of the opioid receptor and opioid peptide families. Although they have considerable sequence homology to the other family members, they are not considered opioid per se because they do not have pharmacological profiles similar to the other family members. The number of NOP receptors in the brain is higher than the other family members, and NOP receptors can be found throughout the brain. Because of the widespread distribution of NOP receptors, N/OFQ and other peptide and small molecule agonists and antagonists have extensive CNS activities. Originally thought to be anti-opioid, NOP receptor agonists block some opioid activities, potentiate others, and modulate other activities not affected by traditional opiates. Because the effect of receptor activation can be dependent upon site of administration, state of the animal, and other variables, the study of NOP receptors has been fraught with contradictions and inconsistencies. In this article, the actions and controversies pertaining to NOP receptor activation and inhibition are discussed with respect to CNS disorders including pain (acute, chronic, and migraine), drug abuse, anxiety and depression. In addition, progress towards clinical use of NOP receptor-directed compounds is discussed.

摘要

阿片肽孤儿受体(NOP)及其内源性配体孤啡肽(N/OFQ)是阿片受体和阿片肽家族的第四种成员。尽管它们与其他家族成员具有相当高的序列同源性,但它们本身并不被认为是阿片类物质,因为它们没有与其他家族成员相似的药理学特征。大脑中的 NOP 受体数量高于其他家族成员,NOP 受体可以在整个大脑中找到。由于 NOP 受体的广泛分布,N/OFQ 和其他肽类和小分子激动剂和拮抗剂具有广泛的中枢神经系统活性。最初被认为是抗阿片类物质,NOP 受体激动剂阻断一些阿片类物质的活性,增强其他活性,调节其他不受传统阿片类物质影响的活性。由于受体激活的效果可能取决于给药部位、动物状态和其他变量,因此 NOP 受体的研究充满了矛盾和不一致。本文讨论了与 NOP 受体激活和抑制有关的作用和争议,涉及包括疼痛(急性、慢性和偏头痛)、药物滥用、焦虑和抑郁在内的中枢神经系统疾病。此外,还讨论了 NOP 受体定向化合物的临床应用进展。