Rai Karan G, Nwakudu Chinwendu U, Szujewski Caroline C, Browe Brigitte M, Fisher Gia E, Sharp Willard W, Tryba Andrew K, Garcia Alfredo J
Department of Medicine, The Section of Emergency Medicine, The University of Chicago, Chicago, Illinois, United States.
The Institute for Integrative Physiology, Section of Pediatric Neurology, The University of Chicago, Chicago, Illinois, United States.
Am J Physiol Lung Cell Mol Physiol. 2025 Jul 1;329(1):L161-L171. doi: 10.1152/ajplung.00302.2024. Epub 2025 Jun 2.
Opioid-induced respiratory depression (OIRD) is the hallmark of opioid overdose and a major risk factor for death due to fentanyl use. Although repeat opioid use (ROU) elevates the risk of death, understanding its influence over breathing and its control has been poorly resolved. We developed a mouse model of recurrent fentanyl use over 5 days to examine how ROU impacts breathing and activity from the pre-Bötzinger complex (preBötC), the brainstem network driving inspiratory rhythmogenesis. Initial fentanyl use caused a profound metabolic crisis during OIRD involving a mismatch between ventilation and oxygen consumption. By of ROU, 77% of mice exhibited an adaptive ventilatory response following ROU, which was accompanied by an improved relationship between ventilation and oxygen consumption during OIRD. However, in the remaining minority, the adaptive response during OIRD failed to emerge following ROU. This divergence emphasizes the heterogeneity in ventilatory and metabolic outcomes following ROU. Moreover, following ROU, rhythmogenesis in the preBötzinger complex was less sensitive to mu-opioid receptor agonism, indicating that adaptation to ROU involves centrally mediated changes in this brainstem network. These findings reveal a series of physiological changes following ROU, typically resulting in improved ventilation and oxygenation during OIRD. Such changes, or lack of thereof, may contribute to the unpredictable nature of overdose susceptibility among opioid users. Recurring fentanyl use is a significant factor contributing to opioid-related deaths, yet the physiological impact of repeat opioid use on breathing remains poorly understood. This study demonstrates that divergent ventilatory responses to opioids emerge following repeated fentanyl administration. These responses coincide with changes in oxygen consumption and inspiratory rhythmogenesis from the preBötzinger complex. These observations advance an understanding of the physiological basis for susceptibility and tolerance among individuals likely to succumb to opioid overdose.
阿片类药物引起的呼吸抑制(OIRD)是阿片类药物过量的标志,也是使用芬太尼导致死亡的主要危险因素。尽管重复使用阿片类药物(ROU)会增加死亡风险,但对其对呼吸及其控制的影响的了解仍很有限。我们建立了一个在5天内反复使用芬太尼的小鼠模型,以研究ROU如何影响来自前包钦格复合体(preBötC)的呼吸和活动,前包钦格复合体是驱动吸气节律发生的脑干网络。初次使用芬太尼会在OIRD期间引发严重的代谢危机,涉及通气与氧消耗之间的不匹配。到ROU时,77%的小鼠在ROU后表现出适应性通气反应,这伴随着OIRD期间通气与氧消耗之间关系的改善。然而,在其余少数小鼠中,ROU后OIRD期间的适应性反应未能出现。这种差异强调了ROU后通气和代谢结果的异质性。此外,ROU后,前包钦格复合体中的节律发生对μ-阿片受体激动作用的敏感性降低,表明对ROU的适应涉及该脑干网络的中枢介导变化。这些发现揭示了ROU后的一系列生理变化,通常会导致OIRD期间通气和氧合改善。这些变化或缺乏这些变化可能导致阿片类药物使用者过量易感性的不可预测性。反复使用芬太尼是导致阿片类药物相关死亡的一个重要因素,但重复使用阿片类药物对呼吸的生理影响仍知之甚少。这项研究表明,反复给予芬太尼后会出现对阿片类药物不同的通气反应。这些反应与前包钦格复合体的氧消耗和吸气节律发生变化一致。这些观察结果推进了对可能死于阿片类药物过量的个体易感性和耐受性生理基础的理解。
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