Jafal Nader-Mugurel, Stoleru Smaranda, Orban Carmen, Fulga Ion-Gigel
"Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
Department of Anesthesia and Intensive Care, University Emergency Hospital, Bucharest, Romania.
Maedica (Bucur). 2025 Mar;20(1):72-80. doi: 10.26574/maedica.2025.20.1.72.
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.
阿片受体是疼痛的关键调节因子,中枢和外周亚型均有助于镇痛。虽然中枢阿片受体已得到广泛研究,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无呼吸抑制和镇静等中枢副作用,已受到关注。本叙述性综述探讨外周阿片受体的分类、定位和激活,强调它们在炎症性疼痛调节中的作用。这些受体在炎症组织中上调,增强镇痛效果。它们的激活通过抑制兴奋性神经递质释放、激活钾通道和免疫调节来调节伤害性信号传导。外周作用的阿片受体激动剂提供靶向性疼痛缓解,而选择性拮抗剂可减轻阿片类药物引起的便秘,而不影响中枢镇痛。包括角叉菜胶诱导的炎症模型在内的临床前研究,强化了靶向外周阿片受体在疼痛治疗中的潜力。未来的研究应集中于优化这些药物以供临床使用、改进药物递送系统,并将它们整合到多模式疼痛管理策略中。