This work presents the dynamical modelling of cardiac electrical activity using bidomain approach. It focuses on the effects of variation of the ionic model parameters on cardiac wave propagation. Cardiac electrical a...This work presents the dynamical modelling of cardiac electrical activity using bidomain approach. It focuses on the effects of variation of the ionic model parameters on cardiac wave propagation. Cardiac electrical activity is governed by partial differential equations coupled to a system of ordinary differential equations. Numerical simulation of these equations is computationally expensive due to their non-linearity and stiffness. Nevertheless, we adopted the bidomain model due to its ability to reflect the actual cardiac wave propagation. The derived bidomain equations coupled with FitzHugh-Nagumo’s ionic equations were time-discretized using explicit forward Euler method and space-discretized using 2-D network modelling to obtain linearized equations for transmembrane potential Vm, extracellular potential φe and gating variable w. We implemented the discretized model and performed simulation experiments to study the effects of variation of ionic model parameters on the propagation of electrical wave across the cardiac tissue. Time characteristic of transmembrane potential, Vm, in the normal cardiac tissue was obtained by setting the values of ionic model parameters to 0.2, 0.2, 0.7 and 0.8 for excitation rate constant ε1, recovery rate constant ε2, recovery decay constant γ and excitation decay constant β respectively. Changing the values of ε1, ε2 to 0.04 and 0.28 respectively, the obtained Vm showed a time dilation at 0.04 indicating cardiac arrhythmia but no significant change to Vm was observed at 0.28. Also, changing β to 0.3 and 1.1 and γ to 0.4 and 1.2 sequentially, there was no significant change to the time characteristic of Vm. The obtained results revealed that only decrease in ε1, ε2 impacted significantly on the cardiac wave propagation.展开更多
One of the major aims of the International Union of Physiological Sciences (IUPS) Physiome Project is to develop multiscale mathematical and computer models that can be used to help understand human health. We present...One of the major aims of the International Union of Physiological Sciences (IUPS) Physiome Project is to develop multiscale mathematical and computer models that can be used to help understand human health. We present here a small facet of this broad plan that applies to the gastrointestinal system. Specifically, we present an anatomically and physiologically based modelling framework that is capable of simulating normal and pathological electrical activity within the stomach and small intestine. The continuum models used within this framework have been created using anatomical information derived from common medical imaging modalities and data from the Visible Human Project. These models explicitly incorporate the various smooth muscle layers and networks of interstitial cells of Cajal (ICC) that are known to exist within the walls of the stomach and small bowel. Electrical activity within individual ICCs and smooth muscle cells is simulated using a previously published simplified representation of the cell level electrical activity. This simulated cell level activity is incorporated into a bidomain representation of the tissue, allowing electrical activity of the entire stomach or intestine to be simulated in the anatomically derived models. This electrical modelling framework successfully replicates many of the qualitative features of the slow wave activity within the stomach and intestine and has also been used to investigate activity associated with functional uncoupling of the stomach.展开更多
文摘This work presents the dynamical modelling of cardiac electrical activity using bidomain approach. It focuses on the effects of variation of the ionic model parameters on cardiac wave propagation. Cardiac electrical activity is governed by partial differential equations coupled to a system of ordinary differential equations. Numerical simulation of these equations is computationally expensive due to their non-linearity and stiffness. Nevertheless, we adopted the bidomain model due to its ability to reflect the actual cardiac wave propagation. The derived bidomain equations coupled with FitzHugh-Nagumo’s ionic equations were time-discretized using explicit forward Euler method and space-discretized using 2-D network modelling to obtain linearized equations for transmembrane potential Vm, extracellular potential φe and gating variable w. We implemented the discretized model and performed simulation experiments to study the effects of variation of ionic model parameters on the propagation of electrical wave across the cardiac tissue. Time characteristic of transmembrane potential, Vm, in the normal cardiac tissue was obtained by setting the values of ionic model parameters to 0.2, 0.2, 0.7 and 0.8 for excitation rate constant ε1, recovery rate constant ε2, recovery decay constant γ and excitation decay constant β respectively. Changing the values of ε1, ε2 to 0.04 and 0.28 respectively, the obtained Vm showed a time dilation at 0.04 indicating cardiac arrhythmia but no significant change to Vm was observed at 0.28. Also, changing β to 0.3 and 1.1 and γ to 0.4 and 1.2 sequentially, there was no significant change to the time characteristic of Vm. The obtained results revealed that only decrease in ε1, ε2 impacted significantly on the cardiac wave propagation.
文摘One of the major aims of the International Union of Physiological Sciences (IUPS) Physiome Project is to develop multiscale mathematical and computer models that can be used to help understand human health. We present here a small facet of this broad plan that applies to the gastrointestinal system. Specifically, we present an anatomically and physiologically based modelling framework that is capable of simulating normal and pathological electrical activity within the stomach and small intestine. The continuum models used within this framework have been created using anatomical information derived from common medical imaging modalities and data from the Visible Human Project. These models explicitly incorporate the various smooth muscle layers and networks of interstitial cells of Cajal (ICC) that are known to exist within the walls of the stomach and small bowel. Electrical activity within individual ICCs and smooth muscle cells is simulated using a previously published simplified representation of the cell level electrical activity. This simulated cell level activity is incorporated into a bidomain representation of the tissue, allowing electrical activity of the entire stomach or intestine to be simulated in the anatomically derived models. This electrical modelling framework successfully replicates many of the qualitative features of the slow wave activity within the stomach and intestine and has also been used to investigate activity associated with functional uncoupling of the stomach.
