| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cellular Biology |
From the Center for Biomedical Engineering (R.W., A.P.), Division of Cardiology (A.P.), University of Kentucky, Lexington, Ky.
Correspondence to Abhijit Patwardhan, PhD, Wenner-Gren Research Laboratory, Center for Biomedical Engineering, University of Kentucky, Lexington, KY 40506-0070. E-mail abhijit{at}uky.edu
Restitution of action potential duration (APD) is thought to be critical in activation instability. Although restitution is used to predict APD during sequential changes in diastolic interval (DI), currently used protocols to determine restitution do not use sequential changes in DI. We explored restitution using a new pacing protocol to change DI sequentially and independently of APD. Transmembrane potentials were recorded from right ventricular endocardial tissue isolated from six dogs. We used three patterns of DIs: oscillatory, to demonstrate differences in APDs depending on previous activation history; random, to minimize effects of previous activation history, each DI preceding an APD had an equal probability of being short or long; and linear, to compare restitution relationship obtained during sequential changes in DI with those obtained using currently used protocols; DIs mimicked those that resulted using currently used protocols, except that they changed in sequence. During oscillatory DIs, restitution showed bimodal trajectory similar to hysteresis. Decrease in APD during decreasing DIs was faster than increase in APD during increasing DIs. When effects of previous activation history were minimized, we observed that for a given DI there were multiple values of APD. Restitution relationship obtained during sequential changes in DI was shallower than those obtained using currently used protocols. Our results show that the new pacing protocol may permit direct evaluation of effects of memory on APD. Sequential and explicit control of DI suggests that use of a unimodal relationship to predict APD when DIs change in sequence may not be appropriate.
Key Words: action potential duration electrical restitution arrhythmia fibrillation
This article has been cited by other articles:
![]() |
S. C. Toal, T. A. Farid, R. Selvaraj, V. S. Chauhan, S. Masse, J. Ivanov, L. Harris, E. Downar, M. R. Franz, and K. Nanthakumar Short-Term Memory and Restitution During Ventricular Fibrillation in Human Hearts: An In Vivo Study Circ Arrhythm Electrophysiol, October 1, 2009; 2(5): 562 - 570. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. A. Eisner, K. M. Dibb, and A. W. Trafford The mechanism and significance of the slow changes of ventricular action potential duration following a change of heart rate Exp Physiol, May 1, 2009; 94(5): 520 - 528. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zaniboni, F. Cacciani, and N. Salvarani Heart/Cardiac Muscle: Temporal variability of repolarization in rat ventricular myocytes paced with time-varying frequencies Exp Physiol, September 1, 2007; 92(5): 859 - 869. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Shusterman, A. Goldberg, and B. London Upsurge in T-Wave Alternans and Nonalternating Repolarization Instability Precedes Spontaneous Initiation of Ventricular Tachyarrhythmias in Humans Circulation, June 27, 2006; 113(25): 2880 - 2887. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Huang, X. Zhou, W. M. Smith, and R. E. Ideker Restitution Properties During Ventricular Fibrillation in the In Situ Swine Heart Circulation, November 16, 2004; 110(20): 3161 - 3167. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. D. Berger Electrical Restitution Hysteresis: Good Memory or Delayed Response? Circ. Res., March 19, 2004; 94(5): 567 - 569. [Full Text] [PDF] |
||||
|
Circulation Research Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2004 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |