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Modelling fibrinolysis: 1D continuum models

机译:纤维蛋白溶解建模:一维连续模型

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摘要

Fibrinolysis is the enzymatic degradation of the fibrin mesh that stabilizes blood clots. Experiments have shown that coarse clots made of thick fibres sometimes lyse more quickly than fine clots made of thin fibres, despite the fact that individual thick fibres lyse more slowly than individual thin fibres. This paper aims at using a 1D continuum reaction–diffusion model of fibrinolysis to elucidate the mechanism by which coarse clots lyse more quickly than fine clots. Reaction–diffusion models have been the standard tool for investigating fibrinolysis, and have been successful in capturing the wave-like behaviour of lysis seen in experiments. These previous models treat the distribution of fibrin within a clot as homogeneous, and therefore cannot be used directly to study the lysis of fine and coarse clots. In our model, we include a spatially heterogeneous fibrin concentration, as well as a more accurate description of the role of fibrin as a cofactor in the activation of the lytic enzyme. Our model predicts spatio-temporal protein distributions in reasonable quantitative agreement with experimental data. The model also predicts observed behaviour such as a front of lysis moving through the clot with an accumulation of lytic proteins at the front. In spite of the model improvements, however, we find that 1D continuum models are unable to accurately describe the observed differences in lysis behaviour between fine and coarse clots. Features of the problems that lead to the inaccuracy of 1D continuum models are discussed. We conclude that higher-dimensional, multiscale models are required to investigate the effect of clot structure on lysis behaviour.
机译:纤维蛋白溶解是纤维蛋白网的酶促降解,可稳定血凝块。实验表明,由粗纤维制成的粗凝块有时比由细纤维制成的细凝块溶解得更快,尽管事实是,各个粗纤维的溶解比单个细纤维溶解得慢。本文旨在使用纤维蛋白溶解的一维连续反应-扩散模型来阐明粗凝块比细凝块更快溶解的机理。反应扩散模型已经成为研究纤维蛋白溶解的标准工具,并且已经成功地捕获了实验中观察到的波浪状裂解行为。这些先前的模型将血纤维蛋白在血块中的分布视为均匀,因此无法直接用于研究细小和粗大血块的裂解。在我们的模型中,我们包括空间上异质的血纤蛋白浓度,以及血纤蛋白作为辅因子在裂解酶激活中的作用的更准确描述。我们的模型预测与实验数据合理的定量一致的时空蛋白质分布。该模型还预测观察到的行为,例如裂解前沿在血凝块中移动,裂解蛋白在前端积聚。尽管改进了模型,但我们发现一维连续体模型无法准确描述细小和粗大血块之间观察到的裂解行为差异。讨论了导致一维连续模型不准确的问题的特征。我们得出结论,需要高维,多尺度模型来研究凝块结构对裂解行为的影响。

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