cytochrome-c-t and Weight-Loss

Androgen reduces fat mass, although the underlying mechanisms are unknown. Here, we examined the effect of testosterone on heat production and mitochondrial biogenesis. Testosterone-treated mice exhibited elevated heat production. Treatment with testosterone increased the expression level of peroxisome proliferator-activated receptor-γ coactivator-1α (PGC1α), ATP5B and Cox4 in skeletal muscle, but not that in brown adipose tissue and liver. mRNA levels of genes involved in mitochondrial biogenesis were elevated in skeletal muscle isolated from testosterone-treated male mice, but were down-regulated in androgen receptor deficient mice. These results demonstrated that the testosterone-induced increase in energy expenditure is derived from elevated mitochondrial biogenesis in skeletal muscle.

Topics: Androgens; Animals; Blood Glucose; Blotting, Western; Body Weight; Cell Line; Cytochromes c; DNA, Mitochondrial; Eating; Energy Metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mitochondria, Muscle; Muscle Fibers, Skeletal; Muscle, Skeletal; Myoglobin; Nuclear Respiratory Factor 1; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha; Receptors, Androgen; Reverse Transcriptase Polymerase Chain Reaction; Testosterone; Transcription Factors; Troponin; Weight Loss