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外周感觉和肠道 μ 阿片受体的作用:外周镇痛和耐受。

On the Role of Peripheral Sensory and Gut Mu Opioid Receptors: Peripheral Analgesia and Tolerance.

机构信息

Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, Semmelweis University, Nagyvárad tér 4, P.O. Box 370, H-1445 Budapest, Hungary.

Institute of Biochemistry, Biological Research Center, Temesvári krt. 62., H- 6726 Szeged, Hungary.

出版信息

Molecules. 2020 May 26;25(11):2473. doi: 10.3390/molecules25112473.

DOI:10.3390/molecules25112473
PMID:32466522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7321260/
Abstract

There is growing evidence on the role of peripheral µ-opioid receptors (MORs) in analgesia and analgesic tolerance. Opioid analgesics are the mainstay in the management of moderate to severe pain, and their efficacy in the alleviation of pain is well recognized. Unfortunately, chronic treatment with opioid analgesics induces central analgesic tolerance, thus limiting their clinical usefulness. Numerous molecular mechanisms, including receptor desensitization, G-protein decoupling, β-arrestin recruitment, and alterations in the expression of peripheral MORs and microbiota have been postulated to contribute to the development of opioid analgesic tolerance. However, these studies are largely focused on central opioid analgesia and tolerance. Accumulated literature supports that peripheral MORs mediate analgesia, but controversial results on the development of peripheral opioid receptors-mediated analgesic tolerance are reported. In this review, we offer evidence on the consequence of the activation of peripheral MORs in analgesia and analgesic tolerance, as well as approaches that enhance analgesic efficacy and decrease the development of tolerance to opioids at the peripheral sites. We have also addressed the advantages and drawbacks of the activation of peripheral MORs on the sensory neurons and gut (leading to dysbiosis) on the development of central and peripheral analgesic tolerance.

摘要

越来越多的证据表明外周μ-阿片受体(MOR)在镇痛和阿片类药物耐受中发挥作用。阿片类镇痛药是治疗中重度疼痛的主要药物,其缓解疼痛的疗效已得到广泛认可。不幸的是,阿片类药物的慢性治疗会诱导中枢性镇痛耐受,从而限制了其临床应用。许多分子机制,包括受体脱敏、G 蛋白偶联解离、β-arrestin 募集以及外周 MOR 和微生物群表达的改变,都被认为有助于阿片类药物耐受的发展。然而,这些研究主要集中在中枢阿片类药物镇痛和耐受上。越来越多的文献支持外周 MOR 介导镇痛,但关于外周阿片受体介导的镇痛耐受发展的争议结果也有报道。在这篇综述中,我们提供了外周 MOR 激活在镇痛和镇痛耐受中的后果的证据,以及增强外周部位镇痛效果和减少阿片类药物耐受发展的方法。我们还讨论了外周 MOR 对感觉神经元和肠道(导致菌群失调)的激活在中枢和外周镇痛耐受发展中的优缺点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c244/7321260/88fc6b77fec0/molecules-25-02473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c244/7321260/3547d998cdad/molecules-25-02473-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c244/7321260/36bb8416195b/molecules-25-02473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c244/7321260/88fc6b77fec0/molecules-25-02473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c244/7321260/3547d998cdad/molecules-25-02473-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c244/7321260/36bb8416195b/molecules-25-02473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c244/7321260/88fc6b77fec0/molecules-25-02473-g003.jpg

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