| Literature DB >> 17932032 |
Adam R Wende1, Paul J Schaeffer, Glendon J Parker, Christoph Zechner, Dong-Ho Han, May M Chen, Chad R Hancock, John J Lehman, Janice M Huss, Donald A McClain, John O Holloszy, Daniel P Kelly.
Abstract
The transcriptional coactivator peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC-1alpha) has been identified as an inducible regulator of mitochondrial function. Skeletal muscle PGC-1alpha expression is induced post-exercise. Therefore, we sought to determine its role in the regulation of muscle fuel metabolism. Studies were performed using conditional, muscle-specific, PGC-1alpha gain-of-function and constitutive, generalized, loss-of-function mice. Forced expression of PGC-1alpha increased muscle glucose uptake concomitant with augmentation of glycogen stores, a metabolic response similar to post-exercise recovery. Induction of muscle PGC-1alpha expression prevented muscle glycogen depletion during exercise. Conversely, PGC-1alpha-deficient animals exhibited reduced rates of muscle glycogen repletion post-exercise. PGC-1alpha was shown to increase muscle glycogen stores via several mechanisms including stimulation of glucose import, suppression of glycolytic flux, and by down-regulation of the expression of glycogen phosphorylase and its activating kinase, phosphorylase kinase alpha. These findings identify PGC-1alpha as a critical regulator of skeletal muscle fuel stores.Entities:
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Year: 2007 PMID: 17932032 DOI: 10.1074/jbc.M707006200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157