Determinants of heterogeneity, excitation and conduction in the sinoatrial node: a model study

• Published in: PLoS computational biology 2010-12, Vol.6 (12), p.e1001041-e1001041
• Main Authors: Oren, Ronit V, Clancy, Colleen E
• Format: Article
• Language: English
• Subjects: Animals; Biophysics; Cardiovascular Disorders/Arrhythmias, Electrophysiology, and Pacing; Cell Count; Computational Biology; Computer Simulation; Electrophysiology; Experiments; Fibroblasts; Fibroblasts - physiology; Heart Atria - cytology; Hypotheses; Models, Cardiovascular; Physiological aspects; Propagation; Rabbits; Sinoatrial node; Sinoatrial Node - physiology; Sodium Channels; Studies; Time Factors; Vagus Nerve Stimulation
• ISSN: 1553-7358; 1553-734X; 1553-7358
• DOI: 10.1371/journal.pcbi.1001041

The sinoatrial node (SAN) is a complex structure that exhibits anatomical and functional heterogeneity which may depend on: 1) The existence of distinct cell populations, 2) electrotonic influences of the surrounding atrium, 3) the presence of a high density of fibroblasts, and 4) atrial cells intermingled within the SAN. Our goal was to utilize a computer model to predict critical determinants and modulators of excitation and conduction in the SAN. We built a theoretical "non-uniform" model composed of distinct central and peripheral SAN cells and a "uniform" model containing only central cells connected to the atrium. We tested the effects of coupling strength between SAN cells in the models, as well as the effects of fibroblasts and interspersed atrial cells. Although we could simulate single cell experimental data supporting the "multiple cell type" hypothesis, 2D "non-uniform" models did not simulate expected tissue behavior, such as central pacemaking. When we considered the atrial effects alone in a simple homogeneous "uniform" model, central pacemaking initiation and impulse propagation in simulations were consistent with experiments. Introduction of fibroblasts in our simulated tissue resulted in various effects depending on the density, distribution, and fibroblast-myocyte coupling strength. Incorporation of atrial cells in our simulated SAN tissue had little effect on SAN electrophysiology. Our tissue model simulations suggest atrial electrotonic effects as plausible to account for SAN heterogeneity, sequence, and rate of propagation. Fibroblasts can act as obstacles, current sinks or shunts to conduction in the SAN depending on their orientation, density, and coupling.