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外周阿片受体拮抗作用可减轻芬太尼引起的心肺抑制,且无厌恶行为。

Peripheral opioid receptor antagonism alleviates fentanyl-induced cardiorespiratory depression and is devoid of aversive behavior.

作者信息

Ruyle Brian C, Masud Sarah, Kesaraju Rohith, Tahirkheli Mubariz, Modh Juhi, Roth Caroline G, Angulo-Lopera Sofia, Lintz Tania, Higginbotham Jessica A, Massaly Nicolas, Morón Jose A

机构信息

Department of Anesthesiology, Washington University in St. Louis, St. Louis, United States.

Pain Center, Washington University in St. Louis, St. Louis, United States.

出版信息

Elife. 2025 Apr 1;13:RP104469. doi: 10.7554/eLife.104469.

Abstract

Millions of Americans suffering from Opioid Use Disorders face a high risk of fatal overdose due to opioid-induced respiratory depression (OIRD). Fentanyl, a powerful synthetic opioid, is a major contributor to the rising rates of overdose deaths. Reversing fentanyl overdoses has proved challenging due to its high potency and the rapid onset of OIRD. We assessed the contributions of central and peripheral mu opioid receptors (MORs) in mediating fentanyl-induced physiological responses. The peripherally restricted MOR antagonist naloxone methiodide (NLXM) both prevented and reversed OIRD to a degree comparable to that of naloxone (NLX), indicating substantial involvement of peripheral MORs to OIRD. Interestingly, NLXM-mediated OIRD reversal did not produce aversive behaviors observed after NLX. We show that neurons in the nucleus of the solitary tract (nTS), the first central synapse of peripheral afferents, exhibit a biphasic activity profile following fentanyl exposure. NLXM pretreatment attenuates this activity, suggesting that these responses are mediated by peripheral MORs. Together, these findings establish a critical role for peripheral MORs, including ascending inputs to the nTS, as sites of dysfunction during OIRD. Furthermore, selective peripheral MOR antagonism could be a promising therapeutic strategy for managing OIRD by sparing CNS-driven acute opioid-associated withdrawal and aversion observed after NLX.

摘要

数以百万计患有阿片类药物使用障碍的美国人因阿片类药物引起的呼吸抑制(OIRD)而面临致命过量的高风险。芬太尼是一种强效合成阿片类药物,是过量死亡人数上升的主要原因。由于其高效力和OIRD的快速发作,逆转芬太尼过量已被证明具有挑战性。我们评估了中枢和外周μ阿片受体(MORs)在介导芬太尼诱导的生理反应中的作用。外周限制性MOR拮抗剂甲硫碘化纳洛酮(NLXM)在预防和逆转OIRD方面的程度与纳洛酮(NLX)相当,这表明外周MORs在很大程度上参与了OIRD。有趣的是,NLXM介导的OIRD逆转并未产生NLX后观察到的厌恶行为。我们发现,孤束核(nTS)中的神经元是外周传入神经的第一个中枢突触,在接触芬太尼后表现出双相活动模式。NLXM预处理减弱了这种活动,表明这些反应是由外周MORs介导的。总之,这些发现确立了外周MORs的关键作用,包括向nTS的上行输入,作为OIRD期间功能障碍的部位。此外,选择性外周MOR拮抗作用可能是一种有前途的治疗策略,通过避免中枢神经系统驱动的急性阿片类药物相关戒断和NLX后观察到的厌恶来管理OIRD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/409f/11961120/6078b9f14ea5/elife-104469-fig1.jpg

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