Circulation, Vol 76, 226-236, Copyright © 1987 by American Heart Association
T Osaka, I Kodama, N Tsuboi, J Toyama and K Yamada
The influence of activation sequences on action potential configuration,
especially in the repolarization phase, was examined in isolated canine
ventricular muscles. Action potentials were recorded from the epicardial
surface in the center of a preparation having nearly uniform fiber
orientation (25 X 25 mm). Stimuli applied just adjacent to the recording
site produced nearly centrifugal propagation. An activation sequence either
parallel (longitudinal) or perpendicular (transverse) to the long axis of
the muscle fibers was produced by peripheral stimulation. Action potential
duration at -60 mV (APD-60 mV) during centrifugal propagation was
significantly longer than that during longitudinal propagation. Further
shortening of APD-60 mV was observed during transverse propagation. When a
collision of longitudinal or transverse wavefronts (longitudinal or
transverse collision) was produced at the action potential recording site,
the shortest APD was recorded. During centrifugal propagation, action
potential mapping around the stimulating electrodes revealed that APD- 60
mV shortened gradually as the recording site was moved further from the
stimulation site. The spatial gradient of APD was steeper in the transverse
than in the longitudinal direction, causing a distortion in the
repolarization sequence and the recovery of excitability near the center of
the tissue. Premature stimuli applied to an area near the central
stimulation site induced one-way block and circus movement of the
wavefront, indicating reentry of excitation. We concluded that the
activation sequence and anisotropic cellular geometry substantially affect
APD, and that such a change contributes to the spatial inhomogeneity of
refractoriness leading to reentrant arrhythmias.
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Effects of activation sequence and anisotropic cellular geometry on the repolarization phase of action potential of dog ventricular muscles
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