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肝脏中血液、组织间液流动及淋巴生成的数学模型。

Mathematical model of blood and interstitial flow and lymph production in the liver.

作者信息

Siggers Jennifer H, Leungchavaphongse Kritsada, Ho Chong Hang, Repetto Rodolfo

机构信息

Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK,

出版信息

Biomech Model Mechanobiol. 2014 Apr;13(2):363-78. doi: 10.1007/s10237-013-0516-x. Epub 2013 Aug 2.

Abstract

We present a mathematical model of blood and interstitial flow in the liver. The liver is treated as a lattice of hexagonal 'classic' lobules, which are assumed to be long enough that end effects may be neglected and a two-dimensional problem considered. Since sinusoids and lymphatic vessels are numerous and small compared to the lobule, we use a homogenized approach, describing the sinusoidal and interstitial spaces as porous media. We model plasma filtration from sinusoids to the interstitium, lymph uptake by lymphatic ducts, and lymph outflow from the liver surface. Our results show that the effect of the liver surface only penetrates a depth of a few lobules' thickness into the tissue. Thus, we separately consider a single lobule lying sufficiently far from all external boundaries that we may regard it as being in an infinite lattice, and also a model of the region near the liver surface. The model predicts that slightly more lymph is produced by interstitial fluid flowing through the liver surface than that taken up by the lymphatic vessels in the liver and that the non-peritonealized region of the surface of the liver results in the total lymph production (uptake by lymphatics plus fluid crossing surface) being about 5% more than if the entire surface were covered by the Glisson-peritoneal membrane. Estimates of lymph outflow through the surface of the liver are in good agreement with experimental data. We also study the effect of non-physiological values of the controlling parameters, particularly focusing on the conditions of portal hypertension and ascites. To our knowledge, this is the first attempt to model lymph production in the liver. The model provides clinically relevant information about lymph outflow pathways and predicts the systemic response to pathological variations.

摘要

我们提出了一种肝脏中血液和组织间液流动的数学模型。肝脏被视为由六边形“经典”小叶组成的晶格结构,假定这些小叶足够长,以至于可以忽略端部效应,并将其视为二维问题。由于与小叶相比,肝血窦和淋巴管数量众多且管径较小,我们采用均匀化方法,将肝血窦和组织间隙空间描述为多孔介质。我们对从肝血窦到组织间隙的血浆滤过、淋巴管对淋巴的摄取以及肝脏表面的淋巴流出进行了建模。我们的结果表明,肝脏表面的影响仅能穿透组织中几个小叶厚度的深度。因此,我们分别考虑一个距离所有外部边界足够远的单个小叶,可将其视为处于无限晶格中,同时也考虑肝脏表面附近区域的模型。该模型预测,流经肝脏表面的组织间液产生的淋巴量略多于肝脏中淋巴管摄取的淋巴量,并且肝脏表面未被腹膜覆盖的区域导致总的淋巴产生量(淋巴管摄取量加上穿过表面的液体量)比整个表面都被格利森腹膜覆盖时多约5%。通过肝脏表面的淋巴流出量估计与实验数据吻合良好。我们还研究了控制参数的非生理值的影响,尤其关注门静脉高压和腹水的情况。据我们所知,这是首次尝试对肝脏中的淋巴生成进行建模。该模型提供了有关淋巴流出途径的临床相关信息,并预测了对病理变化的全身反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14be/3968522/9cf816261717/10237_2013_516_Fig1_HTML.jpg

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