Brain metabolism in health, aging, and neurodegeneration

被引:480
作者
Camandola, Simonetta [1 ]
Mattson, Mark P. [1 ,2 ]
机构
[1] NIA, Neurosci Lab, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
关键词
aging; brain energetics; ketone bodies; metabolism; AGE-RELATED-CHANGES; CEREBRAL GLUCOSE-METABOLISM; KETONE-BODY UTILIZATION; D-BETA-HYDROXYBUTYRATE; BLOOD-BRAIN; ALZHEIMERS-DISEASE; ENERGY-METABOLISM; MONOCARBOXYLATE TRANSPORTER; CEREBROSPINAL-FLUID; MOUSE MODEL;
D O I
10.15252/embj.201695810
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brain cells normally respond adaptively to bioenergetic challenges resulting from ongoing activity in neuronal circuits, and from environmental energetic stressors such as food deprivation and physical exertion. At the cellular level, such adaptive responses include the "strengthening" of existing synapses, the formation of new synapses, and the production of new neurons from stem cells. At the molecular level, bioenergetic challenges result in the activation of transcription factors that induce the expression of proteins that bolster the resistance of neurons to the kinds of metabolic, oxidative, excitotoxic, and proteotoxic stresses involved in the pathogenesis of brain disorders including stroke, and Alzheimer's and Parkinson's diseases. Emerging findings suggest that lifestyles that include intermittent bioenergetic challenges, most notably exercise and dietary energy restriction, can increase the likelihood that the brain will function optimally and in the absence of disease throughout life. Here, we provide an overview of cellular and molecular mechanisms that regulate brain energy metabolism, how such mechanisms are altered during aging and in neurodegenerative disorders, and the potential applications to brain health and disease of interventions that engage pathways involved in neuronal adaptations to metabolic stress.
引用
收藏
页码:1474 / 1492
页数:19
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