神经退行性变
线粒体
神经科学
生物能学
生物
神经病理学
平衡
氧化应激
能量稳态
能量代谢
中枢神经系统
疾病
细胞生物学
医学
病理
内分泌学
肥胖
作者
Diogo Trigo,Catarina Avelar,Miguel X. Fernandes,Juliana M. Sá,Odete A. B. da Cruz e Silva
出处
期刊:FEBS Letters
[Wiley]
日期:2022-02-03
卷期号:596 (9): 1095-1110
被引量:51
标识
DOI:10.1002/1873-3468.14298
摘要
Mitochondria are associated with various cellular activities critical to homeostasis, particularly in the nervous system. The plastic architecture of the mitochondrial network and its dynamic structure play crucial roles in ensuring that varying energetic demands are rapidly met to maintain neuronal and axonal energy homeostasis. Recent evidence associates aging and neurodegeneration with anomalous neuronal metabolism as age‐dependent alterations of neuronal metabolism are now believed to occur prior to neurodegeneration. The brain has a high energy demand, which makes it particularly sensitive to mitochondrial dysfunction. Distinct cellular events causing oxidative stress or disruption of metabolism and mitochondrial homeostasis can trigger a neuropathology. This review explores the bioenergetic hypothesis for the neurodegenerative pathomechanisms, discussing factors leading to age‐related brain hypometabolism and its contribution to cognitive decline. Recent research on the mitochondrial network in healthy nervous system cells, its response to stress, and how it is affected by pathology, as well as current contributions to novel therapeutic approaches will be highlighted.
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