Preservation of mitochondrial membrane potential is necessary for lifespan extension from dietary restriction

被引:9
|
作者
Berry, Brandon J. J. [1 ]
Mjelde, Evan [1 ]
Carreno, Fatima [1 ]
Gilham, Kathryn [1 ]
Hanson, Emily J. J. [1 ]
Na, Emily [1 ]
Kaeberlein, Matt [1 ]
机构
[1] Univ Washington, Dept Lab Med & Pathol, Med Ctr, 1959 NE Pacific St, Seattle, WA 98195 USA
关键词
Calorie restriction; Fasting; Aging; Metabolism; Mitochondrial uncoupling; Bioenergetics; TERM CALORIE RESTRICTION; CAENORHABDITIS-ELEGANS; PROTON LEAK; PROTEIN; BIOGENESIS; MECHANISMS; EXPRESSION; LONGEVITY; GENETICS; INCREASE;
D O I
10.1007/s11357-023-00766-w
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Dietary restriction (DR) increases lifespan in many organisms, but its underlying mechanisms are not fully understood. Mitochondria play a central role in metabolic regulation and are known to undergo changes in structure and function in response to DR. Mitochondrial membrane potential (Delta psi(m)) is the driving force for ATP production and mitochondrial outputs that integrate many cellular signals. One such signal regulated by Delta psi(m) is nutrient-status sensing. Here, we tested the hypothesis that DR promotes longevity through preserved Delta psi(m) during adulthood. Using the nematode Caenorhabditis elegans, we find that Delta psi(m) declines with age relatively early in the lifespan, and this decline is attenuated by DR. Pharmacologic depletion of Delta psi(m) blocked the longevity and health benefits of DR. Genetic perturbation of Delta psi(m) and mitochondrial ATP availability similarly prevented lifespan extension from DR. Taken together, this study provides further evidence that appropriate regulation of Delta psi(m) is a critical factor for health and longevity in response to DR.
引用
收藏
页码:1573 / 1581
页数:9
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