| Literature DB >> 20074528 |
Alexey E Alekseev1, Santiago Reyes, Satsuki Yamada, Denice M Hodgson-Zingman, Srinivasan Sattiraju, Zhiyong Zhu, Ana Sierra, Marina Gerbin, William A Coetzee, David J Goldhamer, Andre Terzic, Leonid V Zingman.
Abstract
Metabolic processes that regulate muscle energy use are major determinants of bodily energy balance. Here, we find that sarcolemmal ATP-sensitive K(+) (K(ATP)) channels, which couple membrane excitability with cellular metabolic pathways, set muscle energy expenditure under physiological stimuli. Disruption of K(ATP) channel function provoked, under conditions of unaltered locomotor activity and blood substrate availability, an extra energy cost of cardiac and skeletal muscle performance. Inefficient fuel metabolism in K(ATP) channel-deficient striated muscles reduced glycogen and fat body depots, promoting a lean phenotype. The propensity to lesser body weight imposed by K(ATP) channel deficit persisted under a high-fat diet, yet obesity restriction was achieved at the cost of compromised physical endurance. Thus, sarcolemmal K(ATP) channels govern muscle energy economy, and their downregulation in a tissue-specific manner could present an antiobesity strategy by rendering muscle increasingly thermogenic at rest and less fuel efficient during exercise. 2010 Elsevier Inc.Entities:
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Year: 2010 PMID: 20074528 PMCID: PMC2849280 DOI: 10.1016/j.cmet.2009.11.009
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287