Cardiac microstructure - Implications for electrical, propagation and defibrillation in the heart

被引:186
作者
Hooks, DA [1 ]
Tomlinson, KA [1 ]
Marsden, SG [1 ]
LeGrice, IJ [1 ]
Smaill, BH [1 ]
Pullan, AJ [1 ]
Hunter, PJ [1 ]
机构
[1] Univ Auckland, Sch Med, Dept Physiol, Bioengn Res Grp, Auckland 1, New Zealand
关键词
bidomain model; defibrillation; finite elements; anisotropy; discontinuous conduction;
D O I
10.1161/01.RES.0000031957.70034.89
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Our understanding of the electrophysiological properties of the heart is incomplete. We have investigated two issues that are fundamental to advancing that understanding. First, there has been widespread debate over the mechanisms by which an externally applied shock can influence a sufficient volume of heart tissue to terminate cardiac fibrillation. Second, it has been uncertain whether cardiac tissue should be viewed as an electrically orthotropic structure, or whether its electrical properties are, in fact, isotropic in the plane orthogonal to myofiber direction. In the present study, a computer model that incorporates a detailed three-dimensional representation of cardiac muscular architecture is used to investigate these issues. We describe a bidomain model of electrical propagation solved in a discontinuous domain that accurately represents the microstructure of a transmural block of rat left ventricle. From analysis of the model results, we conclude that (1) the laminar organization of myocytes determines unique electrical properties in three microstructurally defined directions at any point in the ventricular wall of the heart, and (2) interlaminar clefts between layers of cardiornyocytes provide a substrate for bulk activation of the ventricles during defibrillation.
引用
收藏
页码:331 / 338
页数:8
相关论文
共 37 条
[1]   RECONSTRUCTION OF ACTION POTENTIAL OF VENTRICULAR MYOCARDIAL FIBERS [J].
BEELER, GW ;
REUTER, H .
JOURNAL OF PHYSIOLOGY-LONDON, 1977, 268 (01) :177-210
[2]  
CAULFIELD JB, 1979, LAB INVEST, V40, P364
[3]   Three-dimensional residual strain in midanterior canine left ventricle [J].
Costa, KD ;
MayNewman, K ;
Farr, D ;
ODell, WG ;
McCulloch, AD ;
Omens, JH .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (04) :H1968-H1976
[4]   A SIMULATION STUDY OF THE VENTRICULAR MYOCARDIAL ACTION-POTENTIAL [J].
DROUHARD, JP ;
ROBERGE, FA .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1982, 29 (07) :494-502
[5]   SPREAD OF ACTIVATION IN THE LEFT VENTRICULAR WALL OF THE DOG .3. TRANSMURAL AND INTRAMURAL ANALYSIS [J].
DURRER, D ;
VANDERTWEEL, LH ;
BLICKMAN, JR .
AMERICAN HEART JOURNAL, 1954, 48 (01) :13-35
[6]   FRACTIONATED ELECTROGRAMS FROM A COMPUTER-MODEL OF HETEROGENEOUSLY UNCOUPLED ANISOTROPIC VENTRICULAR MYOCARDIUM [J].
ELLIS, WS ;
AUSLANDER, DM ;
LESH, MD .
CIRCULATION, 1995, 92 (06) :1619-1626
[7]   Activation of cardiac tissue by extracellular electrical shocks -: Formation of 'secondary sources' at intercellular clefts in monolayers of cultured myocytes [J].
Fast, VG ;
Rohr, S ;
Gillis, AM ;
Kléber, AG .
CIRCULATION RESEARCH, 1998, 82 (03) :375-385
[8]  
Feneis H., 1943, MORPHOLOGISCHES JB, V89, P371
[9]   TRANSMURAL ACTIVATIONS AND STIMULUS POTENTIALS IN 3-DIMENSIONAL ANISOTROPIC CANINE MYOCARDIUM [J].
FRAZIER, DW ;
KRASSOWSKA, W ;
CHEN, PS ;
WOLF, PD ;
DANIELEY, ND ;
SMITH, WM ;
IDEKER, RE .
CIRCULATION RESEARCH, 1988, 63 (01) :135-146
[10]  
GARDNER P, 1985, CIRCULATION, V69, P369