Hallmarks of Brain Aging: Adaptive and Pathological Modification by Metabolic States

被引:891
作者
Mattson, Mark P. [1 ,2 ]
Arumugam, Thiruma V. [3 ,4 ]
机构
[1] NIA, Lab Neurosci, Intramural Res Program, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore, Singapore
[4] Sungkyunkwan Univ, Sch Pharm, Suwon 16419, South Korea
关键词
GRAY-MATTER VOLUME; DIET-INDUCED OBESITY; NF-KAPPA-B; INSULIN-RECEPTOR SUBSTRATE; NEURAL PROGENITOR CELLS; OXIDATIVE DNA-DAMAGE; DEFAULT-MODE NETWORK; TOLL-LIKE RECEPTORS; AGE-RELATED DECLINE; PARKINSONS-DISEASE;
D O I
10.1016/j.cmet.2018.05.011
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
During aging, the cellular milieu of the brain exhibits tell-tale signs of compromised bioenergetics, impaired adaptive neuroplasticity and resilience, aberrant neuronal network activity, dysregulation of neuronal Ca2+ homeostasis, the accrual of oxidatively modified molecules and organelles, and inflammation. These alterations render the aging brain vulnerable to Alzheimer's and Parkinson's diseases and stroke. Emerging findings are revealing mechanisms by which sedentary overindulgent lifestyles accelerate brain aging, whereas lifestyles that include intermittent bioenergetic challenges (exercise, fasting, and intellectual challenges) foster healthy brain aging. Here we provide an overview of the cellular and molecular biology of brain aging, how those processes interface with disease-specific neurodegenerative pathways, and how metabolic states influence brain health.
引用
收藏
页码:1176 / 1199
页数:24
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