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Circulation. 1998;97:1810-1817

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(Circulation. 1998;97:1810-1817.)
© 1998 American Heart Association, Inc.


Basic Science Reports

Evolution and Resolution of Long-term Cardiac Memory

Alexei Shvilkin, MD, PhD; Peter Danilo, Jr, PhD; Jie Wang, PhD; Daniel Burkhoff, MD, PhD; Evgeny P. Anyukhovsky, PhD; Eugene A. Sosunov, PhD; Motoki Hara, MD; ; Michael R. Rosen, MD

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

Background—Cardiac 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 Results—Dogs were paced from the ventricles at rates of 110 to 120 bpm for {approx}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.

Conclusions—CM 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.


Key Words: action potentials • electrocardiography • electrophysiology • T-waves • pacing




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