From the Departments of Pharmacology, Pediatrics and Medicine, College of
Physicians and Surgeons of Columbia University, New York, NY.
Correspondence to Michael R. Rosen, MD, Gustavus A. Pfeiffer Professor of Pharmacology, Professor of Pediatrics, College of Physicians and Surgeons of Columbia University, Department of Pharmacology, 630 W 168 St, PH 7West-321, New York, NY 10032. E-mail franeye{at}cudept.cis.columbia.edu
BackgroundCardiac memory (CM)
refers to T-wave changes induced by ventricular pacing or
arrhythmia that accumulate in magnitude and duration with
repeated episodes of abnormal activation. We report herein the kinetics
of long-term CM and its association with the ventricular
action potential.
Methods and ResultsDogs were paced from the ventricles at rates
of 110 to 120 bpm for
ConclusionsCM is a dynamic process for which the final T vector
is predicted by the paced QRS vector and which is associated with
significant changes in epicardial and endocardial but not midmyocardial
cell action potential duration, such that the transmural gradient of
repolarization is altered. It is unaccompanied by evidence of altered
hemodynamics or flow, requires a change in pathway of
activation, and appears to require new protein synthesis.
© 1998 American Heart Association, Inc.
Basic Science Reports
Evolution and Resolution of Long-term Cardiac Memory
3 weeks. CM characterized by gradual sinus
rhythm T vector rotation toward the paced QRS vector evolved in all
dogs regardless of pacing site (left ventricular [LV]
anterior apex or base, posterior LV, or right ventricular
free wall). Cardiac hemodynamics and myocardial flow
(microsphere studies) were unaltered by the pacing. Recovery
time for the memory T wave to return to control increased with duration
of the previous pacing. The protein synthesis inhibitor
cycloheximide markedly (P<.05) and reproducibly
attenuated evolution of CM. When pacing was performed from the atrium,
CM did not occur. Standard microelectrode techniques were used to study
action potential from the LV free wall of control and CM dogs. CM was
associated with increased action potential duration in epicardial and
endocardial but not midmyocardial cells, significantly altering the
transmyocardial gradient for repolarization.
Key Words: action potentials electrocardiography electrophysiology T-waves pacing
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