• DocumentCode
    319951
  • Title

    Simulation study of epicardial action potential under normal and ischemic conditions

  • Author

    Torres, V. ; Ferrero, Jose M. ; Monserrat, M. ; Saiz, J. ; Ferrero, Jose M. ; Thakor, Nitish V.

  • Author_Institution
    D.I.E., Univ. Politecnica de Valencia, Spain
  • fYear
    1997
  • fDate
    7-10 Sep 1997
  • Firstpage
    501
  • Lastpage
    504
  • Abstract
    A computer model has been used to simulate the effects of activation of the ATP sensitive K+ channels on the action potential morphology and duration of canine-type epicardial myocytes. Simulations were based on a modified version of the Luo-Rudy mammalian action potential model. The authors´ formulation of IKATP and the transient outward current (Ito) were included in this model. Their results show that the same fraction of open K-ATP channels has a more pronounced effect in epicardium than in endocardium. They conclude that the presence of a prominent outward current in epicardial but not in endocardial myocytes increases the APD reduction produced by the activation of the K-ATP channels and thus contributes to the dispersion of APD observed under ischemic conditions
  • Keywords
    bioelectric potentials; biomembrane transport; cardiology; digital simulation; physiological models; ATP sensitive K+ channels activation; Luo-Rudy mammalian action potential model; action potential morphology; canine-type epicardial myocytes; cardiac electrophysiology; computer model; endocardium; epicardial action potential; ischemic conditions; normal conditions; open K-ATP channels; transient outward current; Biomedical computing; Biomedical engineering; Calcium; Computational modeling; Computer simulation; Equations; Humans; Ischemic pain; Morphology; Rabbits;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Computers in Cardiology 1997
  • Conference_Location
    Lund
  • ISSN
    0276-6547
  • Print_ISBN
    0-7803-4445-6
  • Type

    conf

  • DOI
    10.1109/CIC.1997.647944
  • Filename
    647944