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内源性和外源性阿片类药物在疼痛中的作用。

Endogenous and Exogenous Opioids in Pain.

机构信息

Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, California 94304, USA; email:

Department of Molecular and Cellular Physiology, Stanford University, Palo Alto, California 94304, USA.

出版信息

Annu Rev Neurosci. 2018 Jul 8;41:453-473. doi: 10.1146/annurev-neuro-080317-061522. Epub 2018 May 31.

Abstract

Opioids are the most commonly used and effective analgesic treatments for severe pain, but they have recently come under scrutiny owing to epidemic levels of abuse and overdose. These compounds act on the endogenous opioid system, which comprises four G protein-coupled receptors (mu, delta, kappa, and nociceptin) and four major peptide families (β-endorphin, enkephalins, dynorphins, and nociceptin/orphanin FQ). In this review, we first describe the functional organization and pharmacology of the endogenous opioid system. We then summarize current knowledge on the signaling mechanisms by which opioids regulate neuronal function and neurotransmission. Finally, we discuss the loci of opioid analgesic action along peripheral and central pain pathways, emphasizing the pain-relieving properties of opioids against the affective dimension of the pain experience.

摘要

阿片类药物是治疗重度疼痛最常用和最有效的镇痛治疗方法,但由于滥用和过量用药的流行,它们最近受到了审查。这些化合物作用于内源性阿片系统,该系统由四个 G 蛋白偶联受体(μ、δ、κ 和孤啡肽)和四个主要的肽家族(β-内啡肽、脑啡肽、强啡肽和孤啡肽/孤啡肽 FQ)组成。在这篇综述中,我们首先描述了内源性阿片系统的功能组织和药理学。然后,我们总结了目前关于阿片类药物调节神经元功能和神经递质传递的信号机制的知识。最后,我们讨论了阿片类药物在周围和中枢疼痛通路上的镇痛作用部位,强调了阿片类药物对疼痛体验的情感维度的缓解作用。

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Endogenous and Exogenous Opioids in Pain.内源性和外源性阿片类药物在疼痛中的作用。
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Mu Opioid Pharmacology: 40 Years to the Promised Land.μ阿片类药理学:通往应许之地的四十年。
Adv Pharmacol. 2018;82:261-291. doi: 10.1016/bs.apha.2017.09.006. Epub 2017 Nov 15.
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Designing Safer Analgesics via μ-Opioid Receptor Pathways.通过μ-阿片受体途径设计更安全的镇痛药
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