Department of Psychology and Neuroscience Program, Temple University, Philadelphia, PA, 19122, United States.
Department of Psychology and Neuroscience Program, Temple University, Philadelphia, PA, 19122, United States.
Behav Brain Res. 2021 May 7;405:113207. doi: 10.1016/j.bbr.2021.113207. Epub 2021 Feb 25.
Given the increasing prevalence of age-related cognitive decline, it is relevant to consider the factors and mechanisms that might facilitate an individual's resiliency to such deficits. Growing evidence suggests a preeminent role of microglia, the prime mediator of innate immunity within the central nervous system. Human and animal investigations suggest aberrant microglial functioning and neuroinflammation are not only characteristic of the aged brain, but also might contribute to age-related dementia and Alzheimer's Disease. Conversely, accumulating data suggest that modifiable lifestyle factors (MLFs), such as healthy diet, exercise and cognitive engagement, can reliably afford cognitive benefits by potentially suppressing inflammation in the aging brain. The present review highlights recent advances in our understanding of the role for microglia in maintaining brain homeostasis and cognitive functioning in aging. Moreover, we propose an integrated, mechanistic model that postulates an individual's resiliency to cognitive decline afforded by MLFs might be mediated by the mitigation of aberrant microglia activation in aging, and subsequent suppression of neuroinflammation.
鉴于与年龄相关的认知能力下降的患病率不断增加,考虑可能促进个体对这些缺陷的适应能力的因素和机制是很重要的。越来越多的证据表明,小胶质细胞起着突出的作用,小胶质细胞是中枢神经系统中固有免疫的主要介质。人类和动物研究表明,异常的小胶质细胞功能和神经炎症不仅是衰老大脑的特征,而且可能导致与年龄相关的痴呆症和阿尔茨海默病。相反,越来越多的证据表明,可改变的生活方式因素(MLFs),如健康饮食、锻炼和认知参与,通过潜在抑制衰老大脑中的炎症,可可靠地提供认知益处。本综述强调了我们对小胶质细胞在维持大脑内稳态和衰老认知功能中的作用的理解的最新进展。此外,我们提出了一个综合的、机制模型,假设个体对 MLFs 提供的认知能力下降的适应能力可能是通过减轻衰老中小胶质细胞异常激活,并随后抑制神经炎症来介导的。