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Urocortin, a novel neuropeptide with anxiogenic-like properties.
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Orphanin FQ, agonist of orphan opioid receptor ORL1, stimulates feeding in rats.孤啡肽FQ,孤儿阿片受体ORL1的激动剂,可刺激大鼠进食。
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Neurocircuitry of stress: central control of the hypothalamo-pituitary-adrenocortical axis.应激的神经回路:下丘脑-垂体-肾上腺皮质轴的中枢控制
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Nociceptin stimulates locomotion and exploratory behaviour in mice.孤啡肽刺激小鼠的运动和探索行为。
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Orphanin FQ is a functional anti-opioid peptide.
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Nociceptin or antinociceptin: potent spinal antinociceptive effect of orphanin FQ/nociceptin in the rat.痛敏肽或抗痛敏肽:孤啡肽/痛敏肽在大鼠脊髓中的强效抗伤害感受作用
Neuroreport. 1996 Sep 2;7(13):2092-4.
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Intracerebroventricular orphanin FQ/nociceptin suppresses dopamine release in the nucleus accumbens of anaesthetized rats.脑室内孤啡肽/痛敏肽抑制麻醉大鼠伏隔核中的多巴胺释放。
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Eur J Pharmacol. 1996 Sep 12;311(2-3):R7-8. doi: 10.1016/0014-2999(96)00578-x.
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Functional antagonism of mu-, delta- and kappa-opioid antinociception by orphanin FQ.孤啡肽对μ、δ和κ阿片类镇痛作用的功能性拮抗
Neurosci Lett. 1996 Aug 23;214(2-3):131-4. doi: 10.1016/0304-3940(96)12917-7.

孤啡肽作为一种抗焦虑剂,可减轻对应激的行为反应。

Orphanin FQ acts as an anxiolytic to attenuate behavioral responses to stress.

作者信息

Jenck F, Moreau J L, Martin J R, Kilpatrick G J, Reinscheid R K, Monsma F J, Nothacker H P, Civelli O

机构信息

Roche CNS Research, Pharma Division, CH-4070, Basel, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14854-8. doi: 10.1073/pnas.94.26.14854.

DOI:10.1073/pnas.94.26.14854
PMID:9405703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC25127/
Abstract

Orphanin FQ (OFQ, Nociceptin) is a recently discovered 17-amino acid neuropeptide that is structurally related to the opioid peptides but does not bind opioid receptors. OFQ has been proposed to act as an anti-opioid peptide, but its widespread sites of action in the brain suggest that it may have more general functions. Here we show that OFQ plays an important role in higher brain functions because it can act as an anxiolytic to attenuate the behavioral inhibition of animals acutely exposed to stressful/anxiogenic environmental conditions. OFQ anxiolytic-like effects were consistent across several behavioral paradigms generating different types of anxiety states in animals (light-dark preference, elevated plus-maze, exploratory behavior of an unfamiliar environment, pharmacological anxiogenesis, operant conflict) and were observed at low nonsedating doses (0.1-3 nmol, intracerebroventricular). Like conventional anxiolytics, OFQ interfered with regular sensorimotor function at high doses (>3 nmol). Our results show that an important role of OFQ is to act as an endogenous regulator of acute anxiety responses. OFQ, probably in concert with other major neuropeptides, exerts a modulatory role on the central integration of stressful stimuli and, thereby, may modulate anxiety states generated by acute stress.

摘要

孤啡肽(OFQ,痛敏肽)是一种最近发现的由17个氨基酸组成的神经肽,其结构与阿片肽相关,但不与阿片受体结合。有人提出OFQ作为一种抗阿片肽发挥作用,但其在脑中广泛的作用位点表明它可能具有更广泛的功能。在此我们表明,OFQ在高级脑功能中发挥重要作用,因为它可作为一种抗焦虑剂,减轻急性暴露于应激/致焦虑环境条件下动物的行为抑制。OFQ的抗焦虑样作用在几种在动物中产生不同类型焦虑状态的行为范式中是一致的(明暗偏好、高架十字迷宫、陌生环境中的探索行为、药物性致焦虑、操作性冲突),并且在低非镇静剂量(0.1 - 3纳摩尔,脑室内注射)时即可观察到。与传统抗焦虑剂一样,OFQ在高剂量(>3纳摩尔)时会干扰正常的感觉运动功能。我们的结果表明,OFQ的一个重要作用是作为急性焦虑反应的内源性调节剂。OFQ可能与其他主要神经肽协同作用,对应激刺激的中枢整合发挥调节作用,从而可能调节由急性应激产生的焦虑状态。