生物
疾病
寿命
长寿
营养感应
营养不良
模式生物
遗传学
进化生物学
医学
基因
信号转导
内科学
作者
Luigi Fontana,Linda Partridge,Valter D. Longo
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2010-04-15
卷期号:328 (5976): 321-326
被引量:2809
标识
DOI:10.1126/science.1172539
摘要
When the food intake of organisms such as yeast and rodents is reduced (dietary restriction), they live longer than organisms fed a normal diet. A similar effect is seen when the activity of nutrient-sensing pathways is reduced by mutations or chemical inhibitors. In rodents, both dietary restriction and decreased nutrient-sensing pathway activity can lower the incidence of age-related loss of function and disease, including tumors and neurodegeneration. Dietary restriction also increases life span and protects against diabetes, cancer, and cardiovascular disease in rhesus monkeys, and in humans it causes changes that protect against these age-related pathologies. Tumors and diabetes are also uncommon in humans with mutations in the growth hormone receptor, and natural genetic variants in nutrient-sensing pathways are associated with increased human life span. Dietary restriction and reduced activity of nutrient-sensing pathways may thus slow aging by similar mechanisms, which have been conserved during evolution. We discuss these findings and their potential application to prevention of age-related disease and promotion of healthy aging in humans, and the challenge of possible negative side effects.
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