Boundary effects influence velocity of transverse propagation of simulated cardiac action potentials
- PDF / 3,124,296 Bytes
- 9 Pages / 610 x 792 pts Page_size
- 26 Downloads / 170 Views
BioMed Central
Open Access
Research
Boundary effects influence velocity of transverse propagation of simulated cardiac action potentials Nicholas Sperelakis*1, Bijoy Kalloor2 and Lakshminarayanan Ramasamy2 Address: 1Dept. of Molecular & Cellular Physiology, University of Cincinnati College of Medicine, Cincinnati, OH 45267-0576, USA and 2Dept. of Electrical Computer Engineering and Computer Science, University of Cincinnati, College of Engineering, Cincinnati, OH 45221, USA Email: Nicholas Sperelakis* - [email protected]; Bijoy Kalloor - [email protected]; Lakshminarayanan Ramasamy - [email protected] * Corresponding author
Published: 06 September 2005 Theoretical Biology and Medical Modelling 2005, 2:36
doi:10.1186/1742-4682-2-36
Received: 18 July 2005 Accepted: 06 September 2005
This article is available from: http://www.tbiomed.com/content/2/1/36 © 2005 Sperelakis et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Propagation of cardiac action potentialtransverse propagation velocityPSpice simulationsedge/boundary effectselectric field transmission of excitation.
Abstract Background: We previously demonstrated that transverse propagation of excitation (cardiac action potentials simulated with PSpice) could occur in the absence of low-resistance connections (gap – junction channels) between parallel chains of myocardial cells. The transverse transmission of excitation between the chains was strongly dependent on the longitudinal resistance of the interstitial fluid space between the chains: the higher this resistance, the closer the packing of the parallel chains within the bundle. The earlier experiments were carried out with 2-dimensional sheets of cells: 2 × 3, 3 × 4, and 5 × 5 models (where the first number is the number of parallel chains and the second is the number of cells in each chain). The purpose of the present study was to enlarge the model size to 7 × 7, thus enabling the transverse velocities to be compared in models of different sizes (where all circuit parameters are identical in all models). This procedure should enable the significance of the role of edge (boundary) effects in transverse propagation to be determined. Results: It was found that transverse velocity increased with increase in model size. This held true whether stimulation was applied to the entire first chain of cells or only to the first cell of the first chain. It also held true for retrograde propagation (stimulation of the last chain). The transverse resistance at the two ends of the bundle had almost no effect on transverse velocity until it was increased to very high values (e.g., 100 or 1,000 megohms). Conclusion: Because the larger the model size, the smaller the relative edge area, we conclude that the edge effects slow the transverse velocity.
Intr
Data Loading...
