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

机译:周围感觉和肠粘膜阿片受体的作用:周围镇痛和耐受性。

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摘要

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.
机译:越来越多的证据表明外周微阿片受体(MOR)在镇痛和镇痛耐受性中的作用。阿片类镇痛药是中度至重度疼痛管理的主要手段,其减轻疼痛的功效已广为人知。不幸的是,阿片类镇痛药的慢性治疗会引起中枢镇痛耐受性,从而限制了其临床实用性。据推测,包括受体脱敏,G蛋白解偶联,β-arrestin募集以及外周MOR和微生物群表达改变在内的许多分子机制都有助于阿片类镇痛药耐受性的发展。但是,这些研究主要集中在中枢阿片类镇痛和耐受性上。大量文献支持外周MOR介导镇痛作用,但据报道关于外周阿片受体介导的镇痛耐受性发展的争议性结果。在这篇综述中,我们提供了有关镇痛药中外周MOR激活和镇痛耐受性的结果的证据,以及增强镇痛效果并降低对外周部位阿片类药物耐受性的方法。我们还针对中枢和外周镇痛耐受性的发展,探讨了在感觉神经元和肠道上激活外周MOR的利弊(导致营养不良)。

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