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. 2013 Jul 11;22(23):4768–4783. doi: 10.1093/hmg/ddt330

Figure 7.

Figure 7.

Effects of oral UQ10 supplementation on mitochondrial UQ levels and state 3 respiration rate in the liver. (A) UQ10 administration increases the levels of UQ10 in liver mitochondria. Similar to that shown in Figure 6A, liver mitochondria isolated from Mclk1liver-KO mice have ∼15% UQ9 relative to controls (Mclk1loxP/+) and accumulate DMQ9. Mitochondrial UQ10 uptake is similar in Mclk1 knockout livers and controls. UQ10 supplementation has no effect on the endogenous content of DMQ9 and UQ9. The columns represent the mean ± SEM of quinone peak area on HPLC chromatographs normalized to protein amounts. Mitochondrial UQ concentrations are expressed nmol/mg mitochondrial protein. n = 6 mice per group. (B) Liver mitochondria of UQ10-fed Mclk1liver-KO mice show a higher state 3 respiration rate (21%–23% more) for both Complex I and II substrates than those of untreated Mclk1liver-KO mice. Such effect is not seen in control group (Mclk1loxP/+). Columns represent mean value ± SEM of six mice per group. Statistical evaluation was performed using paired t-test. *P < 0.05.