首页> 外文期刊>Biomechanics and Modeling in Mechanobiology >Modeling function–perfusion behavior in liver lobules including tissue, blood, glucose, lactate and glycogen by use of a coupled two-scale PDE–ODE approach
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Modeling function–perfusion behavior in liver lobules including tissue, blood, glucose, lactate and glycogen by use of a coupled two-scale PDE–ODE approach

机译:使用耦合的两尺度PDE-ODE方法对肝小叶包括组织,血液,葡萄糖,乳酸和糖原的功能-灌注行为进行建模

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This study focuses on a two-scale, continuum multicomponent model for the description of blood perfusion and cell metabolism in the liver. The model accounts for a spatial and time depending hydro-diffusion–advection–reaction description. We consider a solid-phase (tissue) containing glycogen and a fluid-phase (blood) containing glucose as well as lactate. The five-component model is enhanced by a two-scale approach including a macroscale (sinusoidal level) and a microscale (cell level). The perfusion on the macroscale within the lobules is described by a homogenized multiphasic approach based on the theory of porous media (mixture theory combined with the concept of volume fraction). On macro level, we recall the basic mixture model, the governing equations as well as the constitutive framework including the solid (tissue) stress, blood pressure and solutes chemical potential. In view of the transport phenomena, we discuss the blood flow including transverse isotropic permeability, as well as the transport of solute concentrations including diffusion and advection. The continuum multicomponent model on the macroscale finally leads to a coupled system of partial differential equations (PDE). In contrast, the hepatic metabolism on the microscale (cell level) was modeled via a coupled system of ordinary differential equations (ODE). Again, we recall the constitutive relations for cell metabolism level. A finite element implementation of this framework is used to provide an illustrative example, describing the spatial and time-depending perfusion–metabolism processes in liver lobules that integrates perfusion and metabolism of the liver.
机译:这项研究的重点是用于描述肝脏血液灌注和细胞代谢的两尺度连续多成分模型。该模型说明了取决于空间和时间的水扩散-平流-反应描述。我们考虑含有糖原的固相(组织)和含有葡萄糖以及乳酸盐的液相(血液)。五分量模型通过包括宏观尺度(正弦水平)和微观尺度(细胞水平)的两尺度方法得到了增强。通过基于多孔介质理论(混合物理论与体积分数的概念)的均质化多相方法描述了小叶内的宏观灌注。从宏观上讲,我们回想起基本的混合模型,控制方程以及包括固体(组织)应力,血压和溶质化学势的本构框架。鉴于运输现象,我们讨论了包括横向各向同性渗透率在内的血流以及包括扩散和对流在内的溶质浓度的运输。宏观上的连续多分量模型最终导致了偏微分方程(PDE)的耦合系统。相反,在微尺度(细胞水平)上的肝代谢是通过常微分方程(ODE)的耦合系统建模的。再次,我们回顾了细胞代谢水平的本构关系。该框架的有限元实现被用来提供一个说明性的例子,描述了整合了肝脏灌注和代谢的肝小叶中空间和时间依赖性的灌注-代谢过程。

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