Journal
ENDOCRINOLOGY
Volume 151, Issue 7, Pages 3125-3132Publisher
ENDOCRINE SOC
DOI: 10.1210/en.2010-0018
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Funding
- National Institute of Neurological Disorders and Stroke [R01-NS51257]
- Natural Sciences and Engineering Research Council of Canada [RGPIN 312458-06]
- NSERC
- Ontario Graduate Scholarship
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Testosterone and other androgens are thought to increase lean body mass and reduce fat body mass in men by activating the androgen receptor. However, the clinical potential of androgens for improving body composition is hampered by our limited understanding of the tissues and cells that promote such changes. Here we show that selective overexpression of androgen receptor in muscle cells (myocytes) of transgenic male rats both increases lean mass percentage and reduces fat mass. Similar changes in body composition are observed in human skeletal actin promoter driving expression of androgen receptor (HSA-AR) transgenic mice and result from acute testosterone treatment of transgenic female HSA-AR rats. These shifts in body composition in HSA-AR transgenic male rats are associated with hypertrophy of type IIb myofibers and decreased size of adipocytes. Metabolic analyses of transgenic males show higher activity of mitochondrial enzymes in skeletal muscle and increased O(2) consumption by the rats. These results indicate that androgen signaling in myocytes not only increases muscle mass but also reduces fat body mass, likely via increases in oxidative metabolism. (Endocrinology 151: 3125-3132, 2010)
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