Emerging roles of oxidative stress in brain aging and Alzheimer's disease

被引:358
作者
Ionescu-Tucker, Andra [1 ]
Cotman, Carl W. [1 ]
机构
[1] Univ Calif Irvine, Dept Neurobiol & Behav, Inst Memory Impairments & Neurol Disorders, Irvine, CA 92697 USA
关键词
Oxidative stress; Alzheimer's disease; Brain aging; Exercise; Cognition; DNA-DAMAGE; LIPID-PEROXIDATION; LIFE-SPAN; VITAMIN-E; A-BETA; NEUROTROPHIC FACTOR; ALDEHYDIC PRODUCT; GENE-REGULATION; EXERCISE; MITOCHONDRIA;
D O I
10.1016/j.neurobiolaging.2021.07.014
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Reactive oxygen species (ROS) are metabolic byproducts that are necessary for physiological function but can be toxic at high levels. Levels of these oxidative stressors increase gradually throughout the lifespan, impairing mitochondrial function and damaging all parts of the body, particularly the central nervous system. Emerging evidence suggests that accumulated oxidative stress may be one of the key mechanisms causing cognitive aging and neurodegenerative diseases such as Alzheimer's disease (AD). Here, we synthesize the current literature on the effect of neuronal oxidative stress on mitochondrial dysfunction, DNA damage and epigenetic changes related to cognitive aging and AD. We further describe how oxidative stress therapeutics such as antioxidants, caloric restriction and physical activity can reduce oxidation and prevent cognitive decline in brain aging and AD. Of the currently available therapeutics, we propose that long term physical activity is the most promising avenue for improving cognitive health by reducing ROS while promoting the low levels required for optimal function. Published by Elsevier Inc. This is an open access article under the CC BY license ( http://creativecommons.org/licenses/by/4.0/ )
引用
收藏
页码:86 / 95
页数:10
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