description): The objective of this proposal is to study the relationship between cardiac tissue structure and the electrical events in the process of defibrillation. Defibrillation current traverses the myocardium along convoluted intracellular and extracellular pathways channeled by the tissue structure. It distributes across cell membranes, thus, inducing change in transmembrane potential throughout the myocardium. It is postulated that in the process of defibrillation, the dominant shock-induced transmembrane potential change in the tissue arises from its macroscopic fibrous organization. In particular, changes in the fiber orientation in space, as well as non-uniformity of the extracellular electric field along fibers, are responsible for large-scale transmembrane potential change in the tissue bulk. These spatially distributed regions of induced membrane depolarization and hyperpolarization affect pre-existing reentrant activations in the fibrillating myocardium . More specifically, graded responses and new activations arise in regions of depolarization at the make of the shock. They combine with excitations emanating from regions of hyperpolarization at the break of the shock to ultimately result in either prevention of further wavefront propagation or, for weak shocks, reinitiation of fibrillation. To test these hypotheses, computer simulations will be carried out in (1) anatomically based rabbit ventricular geometry and fiber architecture, (2) accurate description of myocardial ionic current dynamics under strong electric fields, (3) representation of membrane electroporation, and (4) adequate protocols for the generation of reentrant activation patterns.
The specific aims are to: (i) analyze rigorously the relationship between myocardial fibrous organization and shock-induced transmembrane potential changes, and (ii) characterize the interaction between shock-induced potential change and inherent refractoriness of the fibrillating myocardium. Experimental measurements are proposed to validate the defibrillation model expected to guide experimental design and interpretation of experimental findings related to electrical defibrillation of the heart.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL063195-03
Application #
6390460
Study Section
Cardiovascular and Pulmonary Research A Study Section (CVA)
Program Officer
Dunn, Rosalie
Project Start
1999-08-05
Project End
2004-07-31
Budget Start
2001-08-01
Budget End
2002-07-31
Support Year
3
Fiscal Year
2001
Total Cost
$165,539
Indirect Cost
Name
Tulane University
Department
Biomedical Engineering
Type
Schools of Arts and Sciences
DUNS #
City
New Orleans
State
LA
Country
United States
Zip Code
70118
Chen, Xiaozhong; Hu, Yuxuan; Fetics, Barry J et al. (2011) Unstable QT interval dynamics precedes ventricular tachycardia onset in patients with acute myocardial infarction: a novel approach to detect instability in QT interval dynamics from clinical ECG. Circ Arrhythm Electrophysiol 4:858-66
Jie, Xiao; Trayanova, Natalia A (2010) Mechanisms for initiation of reentry in acute regional ischemia phase 1B. Heart Rhythm 7:379-86
Vadakkumpadan, Fijoy; Arevalo, Hermenegild; Prassl, Anton J et al. (2010) Image-based models of cardiac structure in health and disease. Wiley Interdiscip Rev Syst Biol Med 2:489-506
Jie, Xiao; Gurev, Viatcheslav; Trayanova, Natalia (2010) Mechanisms of mechanically induced spontaneous arrhythmias in acute regional ischemia. Circ Res 106:185-92
Constantino, Jason; Long, Yun; Ashihara, Takashi et al. (2010) Tunnel propagation following defibrillation with ICD shocks: hidden postshock activations in the left ventricular wall underlie isoelectric window. Heart Rhythm 7:953-61
Prassl, Anton J; Kickinger, Ferdinand; Ahammer, Helmut et al. (2009) Automatically generated, anatomically accurate meshes for cardiac electrophysiology problems. IEEE Trans Biomed Eng 56:1318-30
Maleckar, Mary M; Greenstein, Joseph L; Giles, Wayne R et al. (2009) Electrotonic coupling between human atrial myocytes and fibroblasts alters myocyte excitability and repolarization. Biophys J 97:2179-90
Vadakkumpadan, Fijoy; Rantner, Lukas J; Tice, Brock et al. (2009) Image-based models of cardiac structure with applications in arrhythmia and defibrillation studies. J Electrocardiol 42:157.e1-10
Maleckar, Mary M; Greenstein, Joseph L; Giles, Wayne R et al. (2009) K+ current changes account for the rate dependence of the action potential in the human atrial myocyte. Am J Physiol Heart Circ Physiol 297:H1398-410
Akhbardeh, Alireza; Tavakolian, Kouhyar; Gurev, Viatcheslav et al. (2009) Comparative analysis of three different modalities for characterization of the seismocardiogram. Conf Proc IEEE Eng Med Biol Soc 2009:2899-903

Showing the most recent 10 out of 67 publications