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Publication : Muscle uncoupling protein 3 overexpression mimics endurance training and reduces circulating biomarkers of incomplete β-oxidation.

First Author  Aguer C Year  2013
Journal  FASEB J Volume  27
Issue  10 Pages  4213-25
PubMed ID  23825224 Mgi Jnum  J:201172
Mgi Id  MGI:5511110 Doi  10.1096/fj.13-234302
Citation  Aguer C, et al. (2013) Muscle uncoupling protein 3 overexpression mimics endurance training and reduces circulating biomarkers of incomplete beta-oxidation. FASEB J 27(10):4213-4225
abstractText  Exercise substantially improves metabolic health, making the elicited mechanisms important targets for novel therapeutic strategies. Uncoupling protein 3 (UCP3) is a mitochondrial inner membrane protein highly selectively expressed in skeletal muscle. Here we report that moderate UCP3 overexpression (roughly 3-fold) in muscles of UCP3 transgenic (UCP3 Tg) mice acts as an exercise mimetic in many ways. UCP3 overexpression increased spontaneous activity ( approximately 40%) and energy expenditure ( approximately 5-10%) and decreased oxidative stress ( approximately 15-20%), similar to exercise training in wild-type (WT) mice. The increase in complete fatty acid oxidation (FAO; approximately 30% for WT and approximately 70% for UCP3 Tg) and energy expenditure ( approximately 8% for WT and 15% for UCP3 Tg) in response to endurance training was higher in UCP3 Tg than in WT mice, showing an additive effect of UCP3 and endurance training on these two parameters. Moreover, increases in circulating short-chain acylcarnitines in response to acute exercise in untrained WT mice were absent with training or in UCP3 Tg mice. UCP3 overexpression had the same effect as training in decreasing long-chain acylcarnitines. Outcomes coincided with a reduction in muscle carnitine acetyltransferase activity that catalyzes the formation of acylcarnitines. Overall, results are consistent with the conclusions that circulating acylcarnitines could be used as a marker of incomplete muscle FAO and that UCP3 is a potential target for the treatment of prevalent metabolic diseases in which muscle FAO is affected.-Aguer, C., Fiehn, O., Seifert, E. L., Bezaire, V., Meissen, J. K., Daniels, A., Scott, K., Renaud, J.-M., Padilla, M., Bickel, D. R., Dysart, M., Adams, S. H., Harper, M.-E. Muscle uncoupling protein 3 overexpression mimics endurance training and reduces circulating biomarkers of incomplete beta-oxidation.
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