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Altered electrical behavior alongside healed myocardial infarcts (MIs) is associated with increased risk of sudden cardiac death. However, the multidimensional mechanisms are poorly understood and described. This study characterizes, for the first time, the intramural spread of electrical activation in the peri-infarct region of chronic reperfusion MIs. Four sheep were studied 13 wk after antero-apical reperfusion infarction. Extracellular potentials (ECPs) were recorded in a ~20 × 20-mm 2 region adjacent to the infarct boundary (25 plunge needles <0.5-mm diameter with 15 electrodes at 1-mm centers) during multisite stimulation. Infarct geometry and electrode locations were reconstructed from magnetic resonance images. Three-dimensional activation spread was characterized by local activation times and interpolated ECP fields ( n = 191 records). Control data were acquired in 4 non-infarcted sheep ( n = 96 records). Electrodes were distributed uniformly around 15 ± 5% of the intramural infarct boundary. There were marked changes in pacing success and ECP morphology across a functional border zone (BZ) ±2 mm from the boundary. Stimulation adjacent to the infarct boundary was associated with low-amplitude electrical activity within the BZ and delayed activation of surrounding myocardium. Bulk tissue depolarization occurred 3.5-14.6 mm from the pacing site for 39% of stimuli with delays of 4-37 ms, both significantly greater than control ( P < 0.0001). Conduction velocity (CV) adjacent to the infarct was not reduced compared with control, consistent with structure-only computer model results. Insignificant CV slowing, irregular stimulus-site specific activation delays, and obvious indirect activation pathways strongly suggest that the substrate for conduction abnormalities in chronic MI is predominantly structural in nature. NEW & NOTEWORTHY Intramural in vivo measurements of peri-infarct electrical activity were not available before this study. We use pace-mapping in a three-dimensional electrode array to show that a subset of stimuli in the peri-infarct region initiates coordinated myocardial activation some distance from the stimulus site with substantial associated time delays. This is site dependent and heterogeneous and occurs for <50% of ectopic stimuli in the border zone. Furthermore, once coordinated activation is initiated, conduction velocity adjacent to the infarct boundary is not significantly different from control. These results give new insights to peri-infarct electrical activity and do not support the widespread view of uniform electrical remodeling in the border zone of chronic myocardial infarcts, with depressed conduction velocity throughout.

The arrangement of cardiac cells into strand and sheet-like structures within the heart wall, confers important electrical properties onto heart tissue. Unraveling cardiomyocyte architecture in both healthy and diseased hearts is fundamental to understanding the mechanisms generating normal rhythm and arrhythmia. We analyzed five extended volume serial image stacks of normal pig left ventricular tissue. Analysis included: (1) reconstruction of original tissue volume and shape with non-linear correction maps; (2) segmentation and higher-order descriptions, areas and orientations of laminar structures through the heart wall; (3)computation of fiber directions; (4) computation of tissue connectivity using a shell filter. These measures contributed to a deeper and more objective understanding of cardiac tissue structures and their spatial variation than previously possible.

DT-MRI has been widely used to quantify myocardial fiber and laminar orientations. These structural orientations influence both the spread of excitation and the reorganization of the myocardium during contraction and are altered in disease states. Studies have sought to validate DT-MRI but questions remain about the accuracy of the method and its sensitivity to the time post-fixation and imaging parameters, including b-value, number of diffusion directions and image voxel size. The advent of high-spatial resolution ex vivo MRI and structure tensor (ST) analysis provides a means of direct validation of DT-MRI and assessment of sensitivity to the b-value, the number of diffusion directions and the image voxel size. We find that, with the fixation method we used, structure does not change with time (up to 72 hours). We show that DT-MRI and ST/HR-MRI are markedly similar measures of fiber orientation but DT-MRI and ST are much less similar measures of laminar orientation. DT-MRI performance is not sensitive to the number of directions, with similar structural orientations measured with 6 or 12 directions. Likewise, DT-MRI performance is generally insensitive to b-value, but laminar measurement is moderately more accurate at b = 500 than for higher b-values.

A theoretical model of the cross-linking topology of ventricular muscle tissue is developed. Using parameter estimation the terms of the theoretical model are estimated for normal and pathological conditions. The model represents the anisotropic structure of the tissue, reproduces published experimental data and characterizes the role of different tissue components in the observed macroscopic behavior. Changes in the material parameters are consistent with expected structural changes and the model is extended to reproduce force-Calcium relationships. Model results are invoked to argue that semisoft behavior and the material axis anisotropy arise from the constraints on the extracellular matrix cross-linking topology.

The ventricular myocardium has a structure of branching laminae through which course regularly orientated myofibers, an architecture important in excitation and contraction. Quantifying this architecture is vital for understanding normal and disease states in the heart and for assessing their impact on electrical function. These data are also highly important in the construction of scientifically and clinically useful computer models of cardiac electrical behavior. Detailed structural information has previously been obtained from serial imaging. In this work we assess the potential for high-resolution (HR) MRI as a means to furnish useful myoarchitecture and compare and contrast this approach with the growing use of DT. Using rat hearts, we conclude that both approaches have strengths and weaknesses, however, HR-MRI may provide a consistently more robust picture of the myoarchitecture in small hearts.

Background: The anisotropy of cardiac tissue is a key determinant of 3D electric propagation and the stability of activation wave fronts in the heart. The electric properties of ventricular myocardium are widely assumed to be axially anisotropic, with activation propagating most rapidly in the myofiber direction and at uniform velocity transverse to this. We present new experimental evidence that contradicts this view., Methods and Results: For the first time, high-density intramural electric mapping (325 electrodes at approximately 4x4x1-mm spacing) from pig left ventricular tissue was used to reconstruct 3D paced activation surfaces projected directly onto 3D tissue structure imaged throughout the same left ventricular volume. These data from 5 hearts demonstrate that ventricular tissue is electrically orthotropic with 3 distinct propagation directions that coincide with local microstructural axes defined by the laminar arrangement of ventricular myocytes. The maximum conduction velocity of 0.67+/-0.019 ms(-1) was aligned with the myofiber axis. However, transverse to this, the maximum conduction velocity was 0.30+/-0.010 ms(-1), parallel to the myocyte layers and 0.17+/-0.004 ms(-1) normal to them. These orthotropic conduction velocities give rise to preferential activation pathways across the left ventricular free wall that are not captured by structurally detailed computer models, which incorporate axially anisotropic electric properties., Conclusions: Our findings suggest that current views on uniform side-to-side electric coupling in the heart need to be revised. In particular, nonuniform laminar myocardial architecture and associated electric orthotropy should be included in future models of initiation and maintenance of ventricular arrhythmia.