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In this paper, we study an optimal control problem for a coupled non-linear system of reaction-diffusion equations with degenerate diffusion, consisting of two partial differential equations representing the density of cells and the concentration of the chemotactic agent. By controlling the concentration of the chemical substrates, this study can guide the optimal growth of cells. The novelty of this work lies on the direct and dual models that remain in a weak setting, which is uncommon in the recent literature for solving optimal control systems. Moreover, it is known that the adjoint problems offer a powerful approach to quantifying the uncertainty associated with model inputs. However, these systems typically lack closed-form solutions, making it challenging to obtain weak solutions. For that, the well-posedness of the direct problem is first well guaranteed. Then, the existence of an optimal control and the first-order optimality conditions are established. Finally, weak solutions for the adjoint system to the non-linear degenerate direct model, are introduced and investigated.

We study the homogenization of a novel microscopic tridomain system, allowing for a more detailed analysis of the properties of cardiac conduction than the classical bidomain and monodomain models. In (Acta Appl.Math. 179 (2022) 1--35), we detail this model in which gap junctions are considered as the connections between adjacent cells in cardiac muscle and could serve as alternative or supporting pathways for cell-to-cell electrical signal propagation. Departing from this microscopic cellular model, we apply the periodic unfolding method to derive the macroscopic tridomain model. Several difficulties prevent the application of unfolding homogenization results, including the degenerate temporal structure of the tridomain equations and a nonlinear dynamic boundary condition on the cellular membrane. To prove the convergence of the nonlinear terms, especially those defined on the microscopic interface, we use the boundary unfolding operator and a Kolmogorov--Riesz compactness's result., Comment: arXiv admin note: text overlap with arXiv:2201.03914

We present a novel microscopic tridomain model describing the electrical activity in cardiac tissue with dynamical gap junctions. The microscopic tridomain system consists of three PDEs modeling the tissue electrical conduction in the intra-and extra-cellular domains, supplemented by a nonlinear ODE system for the dynamics of the ion channels and the gap junctions. We establish the global existence and uniqueness of the weak solutions to our microscopic tridomain model. The global existence of solution, which constitutes the main result of this paper, is proved by means of an approximate non-degenerate system, the Faedo-Galerkin method, and an appropriate compactness argument.

In this paper, we are dealing with a rigorous homogenization result at two different levels for the bidomain model of cardiac electro-physiology. The first level associated with the mesoscopic structure such that the cardiac tissue consists of extracellular and intracellular domains separated by an interface (the sarcolemma). The second one related to the microscopic structure in such a way that the intracellular medium can only be viewed as a periodical layout of unit cells (mitochondria). At the interface between intra-and extracellular media, the fluxes are given by nonlinear functions of ionic and applied currents. A rigorous homogenization process based on unfolding operators is applied to derive the macroscopic (homogenized) model from our meso-microscopic bidomain model. We apply a three-scale unfolding method in the intracellular problem to obtain its homogenized equation at two levels. The first level upscaling of the intracellular structure yields the mesoscopic equation. The second step of the homogenization leads to obtain the intracellular homogenized equation. To prove the convergence of the nonlinear terms, especially those defined on the microscopic interface, we use the boundary unfolding method and a Kolmogorov-Riesz compactness's result. Next, we use the standard unfolding method to homogenize the extracellular problem. Finally, we obtain, at the limit, a reaction-diffusion system on a single domain (the superposition of the intracellular and extracellular media) which contains the homogenized equations depending on three scales. Such a model is widely used for describing the macroscopic behavior of the cardiac tissue, which is recognized to be an important messengers between the cytoplasm (intracellular) and the other extracellular inside the biological cells. Contents 2020 Mathematics Subject Classification. 65N55 and 35A01 and 35B27 and 35K57 and 65M.., Comment: arXiv admin note: substantial text overlap with arXiv:2201.03412

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.