cGK-Tg mice exhibit giant mitochondria in the skeletal muscle, associated with higher oxygen consumption and fat oxidation. Mice were subjected to respiratory gas analysis after fed on high-fat diet. Total DNA and RNA were extracted from the brown adipose tissue and the quadriceps, and quantitative PCR analysis was performed. A: Oxygen consumption on standard diet (n = 6). ▩, wild type; ■, cGK-Tg. B: Mean oxygen consumption for 24 h on standard or high-fat diet. C: Rectal temperature on standard or high-fat diet (n = 12). D: Mean respiratory quotient for 24 h on standard or high-fat diet (n = 6). E: Mean fat oxidation estimated from the respiratory gas analysis for 24 h on standard or high-fat diet (n = 6). F: Mitochondrial DNA copy number estimated from quantification of mitochondrial and nuclear genome (n = 8). G: Expressions of genes encoding PGC-1α and UCP1 in the brown adipose tissue. The values were standardized to those for the control (wild-type [Wt] mice fed on standard diet) in either group (n = 12). H: Expressions of the genes involved in mitochondrial regulation or fatty acid catabolism in the skeletal muscle (n = 12). Standard diet: □, wild type (control); ▨, cGK-Tg. High-fat diet: ▩, wild type; ■, cGK-Tg. I: Electron microscopic analysis of muscle mitochondria of high-fat–fed cGK-Tg mice. *P < 0.05; **P < 0.01 vs. wild-type mice on the same feeding condition.