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Am J Physiol Heart Circ Physiol 280: H1905-H1915, 2001;
0363-6135/01 $5.00
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Vol. 280, Issue 4, H1905-H1915, April 2001

SPECIAL COMMUNICATION
Localized injury in cardiomyocyte network: a new experimental model of ischemia-reperfusion arrhythmias

Ara Arutunyan1, Daniel R. Webster2, Luther M. Swift1, and Narine Sarvazyan1

1 Department of Physiology and 2 Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, Texas 79430

We developed a new experimental approach to study the effects of local injury in a multicellular preparation and tested the ability of the method to induce reperfusion arrhythmias in cardiomyocyte monolayers. A small region of injury was created using geometrically defined flows of control and ischemia-like solutions. Calcium transients were acquired simultaneously from injured, control, and border zone cells using fluo 4. Superfusion with the injury solution rapidly diminished the amplitude of calcium transients within the injury zone, followed by cessation of cell beating. Reperfusion caused an immediate tachyarrhythmic response in ~17% of experiments, with a wave front propagating from a single cell or small cell cluster within the former injury zone. Inclusion of a gap junction uncoupler (1 mM heptanol) in the injury solution narrowed the functional border and sharply increased the number of ectopic foci and the incidence of reperfusion arrhythmias. The model holds a potential to reveal both micro- and macroscopic features of propagation, conduction, and cell coupling in the normal and diseased myocardium and to serve as a new tool to test antiarrhythmic protocols in vitro.

cultured myocytes; calcium transients; ischemic border zone


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