The neuroimmune system - Where aging and excess alcohol intersect

被引:14
作者
Carlson, Erika R. [1 ]
Guerin, Steven P. [1 ]
Nixon, Kimberly [1 ]
Fonken, Laura K. [1 ,2 ]
机构
[1] Univ Texas Austin, Coll Pharm, Div Pharmacol & Toxicol, Austin, TX 78712 USA
[2] Univ Texas Austin, Coll Pharm, Pharmacol & Toxicol, 107 W Dean Keaton,BME 3 510C, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
alcohol use disorder; astrocytes; ethanol; geriatric; microglia; priming; FIBRILLARY ACIDIC PROTEIN; AGE-RELATED-CHANGES; BINGE ETHANOL EXPOSURE; INFLAMMATORY MEDIATORS; GENE-EXPRESSION; VOLUME LOSS; LIFE-SPAN; GFAP-IMMUNOREACTIVITY; MICROGLIAL ACTIVATION; CIRCULATING CYTOKINES;
D O I
10.1016/j.alcohol.2022.08.009
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
As the percentage of the global population over age 65 grows, and with it a subpopulation of individuals with alcohol use disorder (AUD), understanding the effect of alcohol on the aged brain is of utmost importance. Neuroinflammation is implicated in both natural aging as well as alcohol use, and its role in alterations to brain morphology and function may be exacerbated in aging individuals who drink alcohol to excess. The neuroimmune response to alcohol in aging is complex. The few studies investigating this issue have reported heightened basal activity and either hypo- or hyper-reactivity to an alcohol challenge. This review of preclinical research will first introduce key players of the immune system, then explore changes in neuroimmune function with aging or alcohol alone, with discussion of vulnerable brain regions, changes in cytokines, and varied reactions of microglia and astrocytes. We will then consider different levels of alcohol exposure, relevant animal models of AUD, and neuroimmune activation by alcohol across the lifespan. By identifying key findings, challenges, and targets for future research, we hope to bring more attention and resources to this underexplored area of inquiry. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:153 / 167
页数:15
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