Derivation of a new macroscopic bidomain model including three scales for the electrical activity of cardiac tissue

TL;DR

This paper introduces a novel three-scale asymptotic homogenization approach to derive a comprehensive macroscopic bidomain model for cardiac tissue, integrating microscopic and mesoscopic structures for improved electrical activity simulation.

Contribution

The paper presents a new three-scale homogenization method that captures multi-level heterogeneities in cardiac tissue to derive an advanced macroscopic bidomain model.

Findings

Derived a macroscopic bidomain model incorporating three scales.

Successfully homogenized extracellular and intracellular structures.

Enhanced understanding of cardiac tissue electrical behavior.

Abstract

In the present paper, a new three-scale asymptotic homogenization method is proposed to study the electrical behavior of the cardiac tissue structure with multiple heterogeneities at two different levels. The first level is associated with the mesoscopic structure such that the cardiac tissue is composed of extracellular and intracellular domains. The second level is associated with the microscopic structure in such a way the intracellular medium can only be viewed as a periodical layout of unit cells (mitochondria). Then, we define two kinds of local cells that are obtained by upscaling methods. The homogenization method is based on a power series expansion which allows determining the macroscopic (homogenized) bidomain model from the microscopic bidomain problem at each structural level. First, we use the two-scale asymptotic expansion to homogenize the extracellular problem. Then, we apply a three-scale asymptotic expansion in the intracellular problem to obtain its homogenized equation at two levels. The first upscaling level of the intracellular structure yields the mesoscopic equation and the second step of the homogenization leads to obtain the intracellular homogenized equation. Both the mesoscopic and microscopic information is obtained by homogenization to capture local characteristics inside the cardiac tissue structure. Finally, we obtain the macroscopic bidomain model and the heart domain coincides with the intracellular medium and extracellular one, which are two inter-penetrating and superimposed continua connected at each point by the cardiac cellular membrane. The interest of the proposed method comes from the fact that it combines microscopic and mesoscopic characteristics to obtain a macroscopic description of the electrical behavior of the heart.