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      K ATP Channels in the Cardiovascular System

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      Physiological Reviews
      American Physiological Society

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          Abstract

          K ATP channels are integral to the functions of many cells and tissues. The use of electrophysiological methods has allowed for a detailed characterization of K ATP channels in terms of their biophysical properties, nucleotide sensitivities, and modification by pharmacological compounds. However, even though they were first described almost 25 years ago (Noma 1983, Trube and Hescheler 1984), the physiological and pathophysiological roles of these channels, and their regulation by complex biological systems, are only now emerging for many tissues. Even in tissues where their roles have been best defined, there are still many unanswered questions. This review aims to summarize the properties, molecular composition, and pharmacology of K ATP channels in various cardiovascular components (atria, specialized conduction system, ventricles, smooth muscle, endothelium, and mitochondria). We will summarize the lessons learned from available genetic mouse models and address the known roles of K ATP channels in cardiovascular pathologies and how genetic variation in K ATP channel genes contribute to human disease.

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          Author and article information

          Journal
          Physiol Rev
          Physiol. Rev
          physrev
          physrev
          PHYSREV
          Physiological Reviews
          American Physiological Society (Bethesda, MD )
          0031-9333
          1522-1210
          9 December 2015
          January 2016
          1 January 2017
          : 96
          : 1
          : 177-252
          Affiliations
          Departments of Pediatrics, Physiology & Neuroscience, and Biochemistry and Molecular Pharmacology, NYU School of Medicine, New York, New York
          Article
          PMC4698399 PMC4698399 4698399 PRV-00003-2015
          10.1152/physrev.00003.2015
          4698399
          26660852
          16d10a48-4575-4934-acb1-d73e0eb69b87
          Copyright © 2016 the American Physiological Society
          History
          Funding
          Funded by: 100000050 HHS | NIH | National Heart, Lung, and Blood Institute (NHBLI)
          Award ID: HL085820
          Award ID: HL119209
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