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J Appl Physiol (July 19, 2007). doi:10.1152/japplphysiol.00747.2007
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Submitted on July 12, 2007
Accepted on July 12, 2007

ATP-sensitive Potassium Channels: Metabolic Sensing and Cardioprotection

Leonid Vladimir Zingman1*, Aleksey E Alekseev2, Denice M Zingman-Hodgson3, and Andre Terzic4

1 Internal Medicine, University of Iowa, Carver College of Medicine, Iowa City, Iowa, United States; Pharmacology, Mayo Clinic, Mayo College of Medicine, Rochester, Minnesota, United States
2 Pharmacology, Mayo Clinic, Mayo College of Medicine, Rochester, Minnesota, United States
3 Internal Medicine, University of Iowa, Iowa City, Iowa, United States; Internal Medicine, University of Iowa, Carver College of Medicine, Iowa City, Iowa, United States
4 Pharmacology, Medicine, Mayo Clinic, Mayo College of Medicine, Rochester, Minnesota, United States

* To whom correspondence should be addressed. E-mail: Leonid-Zingman{at}uiowa.edu.

The cardiovascular system operates under a wide scale of demands, ranging from con-ditions of rest to extreme stress. How the heart muscle matches rates of ATP production with utilization is an area of active investigation. ATP-sensitive potassium (KATP) chan-nels serve a critical role in the orchestration of myocardial energetic well-being. KATP channel heteromultimers consist of inwardly-rectifying K+ channels (Kir6.2) and ATP-binding cassette sulfonylurea receptors (SUR2A) that translates local ATP/ADP levels, set by ATPases and phosphotransfer reactions, to the channel pore function. In cells where the mobility of metabolites between intracellular microdomains is limited, coupling of phosphotransfer pathways with KATP channels permits a high-fidelity transduction of nucleotide fluxes into changes in membrane excitability matching energy demands with metabolic resources. This KATP channel-dependent optimization of cardiac action poten-tial duration preserves cellular energy balance at varying workloads. Mutations of KATP channels results in disruption of the nucleotide signaling network and generates a stress-vulnerable phenotype with excessive susceptibility to injury, development of car-diomyopathy, and arrhythmia. Solving the mechanisms underlying the integration of KATP channels into the cellular energy network will advance the understanding of endogenous cardioprotection, and the development of strategies for the management of cardiovascu-lar injury and disease progression.




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