The free radical theory of aging emphasizes cumulative oxidative damage in the genome and intracellular proteins due to reactive oxygen species (ROS), which is a major cause for aging. Caloric restriction (CR) has been known as a representative treatment that prevents aging; however, its mechanism of action remains elusive. Here, we show that CR extends the chronological lifespan (CLS) of budding yeast by maintaining cellular energy levels. CR reduced the generation of total ROS and mitochondrial superoxide; however, CR did not reduce the oxidative damage in proteins and DNA. Subsequently, calorie-restricted yeast had higher mitochondrial membrane potential (MMP), and it sustained consistent ATP levels during the process of chronological aging. Our results suggest that CR extends the survival of the chronologically aged cells by improving the efficiency of energy metabolism for the maintenance of the ATP level rather than reducing the global oxidative damage of proteins and DNA.
Keywords: 2′,7′-dichlorodihydrofluorescein diacetate; 3,3′-dihexyloxacarbocyanine iodide; 8-OHdG; 8-hydroxydeoxyguanosine; ATP; Aging; Budding yeast; CLS; CR; Caloric restriction; Chronological lifespan; DNPH; DiOC(6); ETC; H2DCFDA; RLS; ROS; caloric restriction; chronological lifespan; dinitrophenylhydrazine; electron transport chain; reactive oxygen species; replicative lifespan.
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