Rapamycin reverses age-related increases in mitochondrial ROS production at complex I, oxidative stress, accumulation of mtDNA fragments inside nuclear DNA, and lipofuscin level, and increases autophagy, in the liver of middle-aged mice
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Rapamycin abolishes age-related increases in mitochondrial ROS production and leak at complex I.

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Rapamycin abolishes age-related increases of mtDNA fragments inside nuclear DNA.

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Rapamycin abolishes increases in mitochondrial protein lipoxidation with age.

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Rapamycin increases autophagy and partially abolishes lipofuscin accumulation with age.

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