Proceedings of the National Academy of Sciences · 2020 · 171 citations · 43 references
Life SciencesBiochemistryPhysiologyAgingMetabolismMitochondrial BiologyMitochondrial BiochemistryMitochondrial BioenergeticsMitochondrial MembranesMitochondrial MetabolismMitochondrial PhysiologyOxidative PhosphorylationAtp Synthase RegulationHexokinase RegulationMitochondrial Atp ProductionMitochondrial Atp SynthaseMitochondrial Membrane Potential CollapseMitochondrial Membrane Potential MaintenanceMitochondrial Reactive Oxygen Species ProductionReactive Oxygen Species Modulation
-ATP synthase with ADP until glucose or creatine is available. Under these conditions, the membrane potential, ∆ψ, is maintained at a lower than maximal level (i.e., mild depolarization of mitochondria). This ∆ψ decrease is sufficient to completely inhibit mROS generation. In 2.5-y-old mice, mild depolarization disappears in the skeletal muscles, diaphragm, heart, spleen, and brain and partially in the lung and kidney. This age-dependent decrease in the levels of bound kinases is not observed in NMRs and bats for many years. As a result, ROS-mediated protein damage, which is substantial during the aging of short-lived mice, is stabilized at low levels during the aging of long-lived NMRs and bats. It is suggested that this mitochondrial mild depolarization is a crucial component of the mitochondrial anti-aging system.
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