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Sarcolemmal ATP-sensitive K(+) channels control energy expenditure determining body weight.

Alexey E Alekseev | 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
Cell metabolism | 2010

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.

Pubmed ID: 20074528

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Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: K08 HL093368
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR052777
  • Agency: NIGMS NIH HHS, United States
    Id: T32GM008685
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL064822-05
  • Agency: NHLBI NIH HHS, United States
    Id: R01HL64822
  • Agency: NHLBI NIH HHS, United States
    Id: K08 HL093368-01
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL064822
  • Agency: NIAMS NIH HHS, United States
    Id: AR052777
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM008685

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MetaMorph Microscopy Automation and Image Analysis Software (tool)

RRID:SCR_002368

Software tool for automated microscope acquisition, device control, and image analysis. Used for integrating dissimilar fluorescent microscope hardware and peripherals into a single custom workstation, while providing all the tools needed to perform analysis of acquired images. Offers user friendly application modules for analysis such as cell signaling, cell counting, and protein expression.

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