长寿
氧化应激
蛋氨酸
衰老自由基理论
线粒体
线粒体DNA
热量理论
不饱和度
生物
生物化学
活性氧
氧化磷酸化
化学
遗传学
氨基酸
内分泌学
基因
有机化学
出处
期刊:Progress in Molecular Biology and Translational Science
日期:2014-01-01
卷期号:: 1-27
被引量:143
标识
DOI:10.1016/b978-0-12-394625-6.00001-5
摘要
The mitochondrial free radical theory of aging is reviewed. Only two parameters currently correlate with species longevity in the right sense: the mitochondrial rate of reactive oxygen species (mitROS) production and the degree of fatty acid unsaturation of tissue membranes. Both are low in long-lived animals. In addition, the best-known manipulation that extends longevity, dietary restriction, also decreases the rate of mitROS production and oxidative damage to mtDNA. The same occurs during protein restriction as well as during methionine restriction. These two manipulations also increase maximum longevity in rodents. The decrease in mitROS generation and oxidative stress that takes place in caloric restriction seems to be due to restriction of a single dietary substance: methionine. The information available supports a mitochondrial free radical theory of aging focused on low generation of endogenous damage and low sensitivity of membranes to oxidation in long-lived animals.
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