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Chaos 12, 852 (2002); http://dx.doi.org/10.1063/1.1504242 (41 pages)

Multiple mechanisms of spiral wave breakup in a model of cardiac electrical activity

Flavio H. Fenton1, Elizabeth M. Cherry1, Harold M. Hastings2, and Steven J. Evans1

1Center for Arrhythmia Research at Hofstra University and The Heart Institute, Beth Israel Medical Center, New York, New York 10003
2Center for Arrhythmia Research and Department of Physics, Hofstra University, Hempstead, New York 11549

(Received 14 April 2002; accepted 3 July 2002; published online 23 August 2002)

It has become widely accepted that the most dangerous cardiac arrhythmias are due to reentrant waves, i.e., electrical wave(s) that recirculate repeatedly throughout the tissue at a higher frequency than the waves produced by the heart’s natural pacemaker (sinoatrial node). However, the complicated structure of cardiac tissue, as well as the complex ionic currents in the cell, have made it extremely difficult to pinpoint the detailed dynamics of these life-threatening reentrant arrhythmias. A simplified ionic model of the cardiac action potential (AP), which can be fitted to a wide variety of experimentally and numerically obtained mesoscopic characteristics of cardiac tissue such as AP shape and restitution of AP duration and conduction velocity, is used to explain many different mechanisms of spiral wave breakup which in principle can occur in cardiac tissue. Some, but not all, of these mechanisms have been observed before using other models; therefore, the purpose of this paper is to demonstrate them using just one framework model and to explain the different parameter regimes or physiological properties necessary for each mechanism (such as high or low excitability, corresponding to normal or ischemic tissue, spiral tip trajectory types, and tissue structures such as rotational anisotropy and periodic boundary conditions). Each mechanism is compared with data from other ionic models or experiments to illustrate that they are not model-specific phenomena. Movies showing all the breakup mechanisms are available at http://arrhythmia.hofstra.edu/breakup and at ftp://ftp.aip.org/epaps/chaos/E-CHAOEH-12-039203/ INDEX.html. The fact that many different breakup mechanisms exist has important implications for antiarrhythmic drug design and for comparisons of fibrillation experiments using different species, electromechanical uncoupling drugs, and initiation protocols. © 2002 American Institute of Physics.

© 2002 American Institute of Physics

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KEYWORDS and PACS

PACS

  • 87.19.Hh

    Cardiac dynamics

  • 87.19.R-

    Mechanical and electrical properties of tissues and organs

  • 87.10.-e

    General theory and mathematical aspects

ARTICLE DATA

PUBLICATION DATA

ISSN

1054-1500 (print)  
1089-7682 (online)

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