外伤性脑损伤加剧了酒精消耗和神经炎症,认知和胆碱能活性下降。

IF 6.2 1区 医学 Q1 PSYCHIATRY
Himanshu Gangal, Jaclyn Iannucci, Yufei Huang, Ruifeng Chen, William Purvines, W Taylor Davis, Arian Rivera, Giles Johnson, Xueyi Xie, Sanjib Mukherjee, Valerie Vierkant, Kaley Mims, Katherine O'Neill, Xuehua Wang, Lee A Shapiro, Jun Wang
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引用次数: 0

摘要

创伤性脑损伤(TBI)是一项全球性的健康挑战,在很大程度上导致残疾,并导致30%的损伤相关死亡。每年,全世界发生超过5000万例TBI,许多急诊科的成年TBI患者表现为体内有酒精。脑外伤也是酗酒的一个已知危险因素,但其与饮酒的相互作用仍然知之甚少。在这项研究中,我们证明了雄性C57BL/6小鼠的TBI液体冲击损伤(FPI)模型显著增加酒精消耗并损害认知功能。FPI显著降低纹状体胆碱能中间神经元(CINs)的数量和活性,增加纹状体小胶质细胞。值得注意的是,通过电生理学和乙酰胆碱生物传感测量,通过系统给药PLX 5622消耗小胶质细胞可增强胆碱能活性。这些发现表明,创伤性脑损伤通过激活小胶质细胞和降低胆碱能功能来促进酒精消耗和损害认知能力。这项研究为TBI与酒精使用增加和认知缺陷之间的联系机制提供了重要的见解,可能指导未来的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Traumatic brain injury exacerbates alcohol consumption and neuroinflammation with decline in cognition and cholinergic activity.

Traumatic brain injury (TBI) is a global health challenge that substantially contributes to disability and is responsible for 30% of injury-related deaths. Annually, over 50 million TBIs occur worldwide, with many adult TBI patients in emergency departments presenting with alcohol in their system. TBI is also a known risk factor for alcohol abuse, yet its interaction with alcohol consumption remains poorly understood. In this study, we demonstrate that the fluid percussion injury (FPI) model of TBI in male C57BL/6 mice significantly increases alcohol consumption and impairs cognitive function. FPI markedly reduced the number and activity of striatal cholinergic interneurons (CINs) while increasing striatal microglial cells. Notably, depleting microglial cells by systemic PLX 5622 administration enhanced cholinergic activity, as measured by electrophysiology and acetylcholine biosensing. These findings suggest that TBI promotes alcohol consumption and impairs cognitive abilities through microglia activation and reduced cholinergic function. This research provides critical insight into the mechanisms linking TBI with increased alcohol use and cognitive deficits, potentially guiding future therapeutic strategies.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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