Peripheral Opioid Receptors in the Modulation of Inflammatory Pain: a Narrative Review.

Nader-Mugurel Jafal, Smaranda Stoleru, Carmen Orban, Ion-Gigel Fulga
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Abstract

Opioid receptors are key modulators of pain, with both central and peripheral subtypes contributing to analgesia. While central opioid receptors have been extensively studied, peripheral opioid receptors, located on sensory nerve terminals and immune cells, have gained attention for their ability to provide localized analgesia and anti-inflammatory effects without central side effects such as respiratory depression and sedation. This narrative review explores the classification, localization, and activation of peripheral opioid receptors, emphasizing their role in inflammatory pain modulation. These receptors are upregulated in inflamed tissues, enhancing analgesic efficacy. Their activation modulates nociceptive signaling through inhibition of excitatory neurotransmitter release, potassium channel activation, and immune regulation. Peripherally acting opioid receptor agonists offer targeted pain relief, while selective antagonists mitigate opioid-induced constipation without affecting central analgesia. Preclinical studies, including carrageenaninduced inflammation models, have reinforced the potential of peripheral opioid receptor targeting in pain therapy. Future research should focus on optimizing these agents for clinical use, improving drug delivery systems, and integrating them into multimodal pain management strategies.

外周阿片受体在炎性疼痛调节中的作用:综述。
阿片受体是疼痛的关键调节剂,中枢和外周亚型都有助于镇痛。虽然中枢阿片受体已被广泛研究,但位于感觉神经末梢和免疫细胞上的外周阿片受体因其能够提供局部镇痛和抗炎作用而不产生中枢副作用(如呼吸抑制和镇静)而受到关注。这篇综述探讨了外周阿片受体的分类、定位和激活,强调了它们在炎症性疼痛调节中的作用。这些受体在炎症组织中表达上调,增强了镇痛效果。它们的激活通过抑制兴奋性神经递质释放、钾通道激活和免疫调节来调节伤害性信号。外周作用的阿片受体激动剂提供靶向疼痛缓解,而选择性拮抗剂减轻阿片诱导的便秘而不影响中枢镇痛。临床前研究,包括卡拉胶诱导的炎症模型,已经加强了外周阿片受体靶向治疗疼痛的潜力。未来的研究应侧重于优化这些药物的临床应用,改进给药系统,并将其整合到多模式疼痛管理策略中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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