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(Circulation Research. 2007;101:e103.)
© 2007 American Heart Association, Inc.

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Laminar Arrangement of Ventricular Myocytes Influences Electrical Behavior of the Heart

Darren A. Hooks, Mark L. Trew, Bryan J. Caldwell, Gregory B. Sands, Ian J. LeGrice, Bruce H. Smaill

From the Bioengineering Institute (D.A.H., M.L.T., B.J.C., G.B.S., I.J.L., B.H.S.), and the Department of Physiology, School of Medicine (I.J.L., B.H.S.), University of Auckland, New Zealand.

Correspondence to Dr Darren A. Hooks, Senior Research Fellow, Bioengineering Institute, University of Auckland, Private Bag 92019, Auckland, New Zealand. E-mail d.hooks{at}auckland.ac.nz

The response of the heart to electrical shock, electrical propagation in sinus rhythm, and the spatiotemporal dynamics of ventricular fibrillation all depend critically on the electrical anisotropy of cardiac tissue. A long-held view of cardiac electrical anisotropy is that electrical conductivity is greatest along the myocyte axis allowing most rapid propagation of electrical activation in this direction, and that conductivity is isotropic transverse to the myocyte axis supporting a slower uniform spread of activation in this plane. In this context, knowledge of conductivity in two directions, parallel and transverse to the myofiber axis, is sufficient to characterize the electrical action of the heart. Here we present new experimental data that challenge this view. We have used a novel combination of intramural electrical mapping, and experiment-specific computer modeling, to demonstrate that left ventricular myocardium has unique bulk conductivities associated with three microstructurally-defined axes. We show that voltage fields induced by intramural current injection are influenced by not only myofiber direction, but also the transmural arrangement of muscle layers or myolaminae. Computer models of these experiments, in which measured 3D tissue structure was reconstructed in-silico, best matched recorded voltages with conductivities in the myofiber direction, and parallel and normal to myolaminae, set in the ratio 4:2:1, respectively. These findings redefine cardiac tissue as an electrically orthotropic substrate and enhance our understanding of how external shocks may act to successfully reset the fibrillating heart into a uniform electrical state. More generally, the mechanisms governing the destabilization of coordinated electrical propagation into ventricular arrhythmia need to be evaluated in the light of this discovery.

Key Words: conductivity • electrical mapping • ventricular microstructure • computer modeling

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