mtDNA depletion and energy failure in Sirt2
−/− mice. (A) SIRT2 protein level in spinal cord from WT and Sirt2
−/− mice at 13 months of age (n = 6/genotype), (B) mtDNA levels in spinal cord and cortex (n = 8/genotype), (C) relative mRNA levels of Sirt2, Sirt1, Pgc‐1α, Tfam, and Nrf1 in spinal cord and cortex (n = 8/genotype), (D) SIRT1 protein level in spinal cord (n = 6/genotype), (E) ATP levels in spinal cord and cortex (n = 8/genotype), (F) ex vivo mitochondrial respiration analysis performed on permeabilized sections of spinal cord (n = 5/genotype), and (G) NAD
+, NADH, and NAD
+/NADH ratio in spinal cord and cortex (n = 8/genotype) from WT and Sirt2
−/− mice at 13 months of age. Data represent mean ± SD. Statistical analysis was carried out with Student's t‐test (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001).