Original Contributions |
From the Department of Physiology, University of Berne, Berne, Switzerland.
Correspondence to Vladimir G. Fast, PhD, Cardiac Rhythm Management Laboratory, University of Alabama at Birmingham, B149 Volker Hall, 1670 University Blvd, Birmingham, AL 35294. E-mail fast{at}crml.uab.edu
AbstractThis study investigated the
activation of cardiac tissue by "secondary sources," which are
localized changes of the transmembrane potential (Vm)
during the application of strong extracellular electrical shocks far
from the shock electrodes, in cultures of neonatal rat myocytes. Cell
monolayers with small intercellular clefts (length, 45 to 270
µm; width, 20 to 70 µm [mean±SD, 54±13 µm]; n=46)
were produced using a technique of directed cell growth. Changes in
Vm relative to the action potential amplitude
(
Vm/APA) were measured using a fluorescent
voltage-sensitive dye and a 10x10 photodiode array. Shocks with
voltage gradients of 4 to 18 V/cm were applied across the clefts during
either the action potential (AP) plateau or diastole.
During the AP plateau, shocks induced secondary sources in the form of
localized hyperpolarizations and depolarizations in
the regions immediately adjacent to opposite sides of the clefts. The
strength of the secondary sources, defined as the difference of
Vm/APA across a cleft, increased with increasing cleft
length or increasing electrical field gradient. For shocks with a
gradient of 8.5 V/cm, the estimated critical cleft length necessary to
reach a Vm level corresponding to the diastolic
threshold of excitation was 171±7 µm. Accordingly, shocks with
average strength of 8.2 V/cm applied during diastole
produced secondary sources that directly excited cells adjacent to the
clefts when the cleft length was 196±53 µm (n=14) and that
failed when the cleft length was 84±23 µm (n=9,
P<001). The area of earliest excitation in such cases
coincided with the area of maximal depolarization induced during the
plateau phase. These data suggest that small inexcitable obstacles may
contribute to the Vm changes during the application of
strong extracellular electrical shocks in vivo.
Key Words: stimulation defibrillation optical mapping voltage-sensitive dye cell cultures
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