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创伤性脑损伤与阿片类药物:二十一世纪的双重祸害。

Traumatic Brain Injury and Opioids: Twin Plagues of the Twenty-First Century.

机构信息

Integrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada.

Anesthesiology Department, Lebanese American University Medical Center-Rizk Hospital, Beirut, Lebanon.

出版信息

Biol Psychiatry. 2024 Jan 1;95(1):6-14. doi: 10.1016/j.biopsych.2023.05.013. Epub 2023 May 20.

Abstract

Traumatic brain injury (TBI) and opioid use disorder (OUD) comprise twin plagues causing considerable morbidity and mortality worldwide. As interactions between TBI and OUD are to our knowledge uncharted, we review the possible mechanisms by which TBI may stimulate the development of OUD and discuss the interaction or crosstalk between these two processes. Central nervous system damage due to TBI appears to drive adverse effects of subsequent OUD and opioid use/misuse affecting several molecular pathways. Pain, a neurological consequence of TBI, is a risk factor that increases the likelihood of opioid use/misuse after TBI. Other comorbidities including depression, anxiety, posttraumatic stress disorder, and sleep disturbances are also associated with deleterious outcomes. We examine the hypothesis that a TBI "first hit" induces a neuroinflammatory process involving microglial priming, which, on a second hit related to opioid exposure, exacerbates neuroinflammation, modifies synaptic plasticity, and spreads tau aggregates to promote neurodegeneration. As TBI also impairs myelin repair by oligodendrocytes, it may reduce or degrade white matter integrity in the reward circuit resulting in behavioral changes. Along with approaches focused on specific patient symptoms, understanding the CNS effects following TBI offers a promise of improved management for individuals with OUD.

摘要

创伤性脑损伤(TBI)和阿片类药物使用障碍(OUD)是全球范围内导致高发病率和死亡率的双重祸害。由于 TBI 和 OUD 之间的相互作用我们目前还不了解,我们回顾了 TBI 可能刺激 OUD 发展的可能机制,并讨论了这两个过程之间的相互作用或串扰。TBI 引起的中枢神经系统损伤似乎导致随后的 OUD 和阿片类药物使用/滥用产生不良影响,影响了几个分子途径。疼痛是 TBI 的一种神经学后果,是 TBI 后阿片类药物使用/滥用可能性增加的一个风险因素。其他合并症,包括抑郁、焦虑、创伤后应激障碍和睡眠障碍,也与不良后果有关。我们检验了这样一个假设,即 TBI“首次打击”引发涉及小胶质细胞预激活的神经炎症过程,而与阿片类药物暴露相关的“二次打击”会加剧神经炎症、改变突触可塑性,并传播 tau 聚集物以促进神经退行性变。由于 TBI 还通过少突胶质细胞损害髓鞘修复,它可能会降低或降解奖励回路中的白质完整性,导致行为改变。除了针对特定患者症状的治疗方法外,了解 TBI 后的中枢神经系统影响有望改善 OUD 患者的治疗效果。

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