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首页> 外文期刊>Russian Journal of Numerical Analysis and Mathematical Modelling >Modelling of thrombus growth and growth stop in flow by the method of dissipative particle dynamics
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Modelling of thrombus growth and growth stop in flow by the method of dissipative particle dynamics

机译:耗散粒子动力学方法对血栓生长和生长停止流动的建模

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Platelet aggregation at the site of the vascular injury leads to the formation of a hemostatic plug covering the injury site, or a thrombus in the pathological case. The mechanisms that control clot growth or lead to growth arrest are not yet completely understood. In order to study these mechanisms theoretically, we use the Dissipative Particle Dynamics method, which allows us to model individual platelets in the flow and in the clot. The model takes into account different stages of the platelet adhesion process. First, a platelet is captured reversibly by the aggregate, then it is activated and adheres firmly, becoming a part of its core. We suggest that the core of the clot is composed of platelets unable to attach new platelets from the flow due to their activation by thrombin and/or wrapping by the fibrin mesh. The simulations are in a good agreement with the experimental results [9]. Modelling shows that stopping the growth of a hemostatic plug (and thrombus) may result from its exterior part being removed by the flow and exposed its non-adhesive core to the flow.
机译:在血管损伤部位的血小板聚集导致形成覆盖在损伤部位的止血塞,或者在病理情况下形成血栓。控制血块生长或导致生长停滞的机制尚未完全了解。为了从理论上研究这些机制,我们使用了“耗散粒子动力学”方法,该方法使我们可以对血流和血块中的单个血小板进行建模。该模型考虑了血小板粘附过程的不同阶段。首先,血小板被聚集体可逆地捕获,然后被激活并牢固粘附,成为其核心的一部分。我们建议凝块的核心由血小板组成,这些血小板由于其被凝血酶激活和/或被纤维蛋白网包裹而无法从血流中附着新的血小板。仿真结果与实验结果吻合良好[9]。建模显示,止血塞(和血栓)的停止生长可能是由于其外层部分被血流清除并使其非粘性核心暴露于血流而造成的。

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    Institut Camille Jordan, UMR 5208 CNRS, University Lyon 1, 69622 Villeurbanne, France,INRIA Team Dracula, INRIA Antenne Lyon la Doua, 69603 Villeurbanne, France;

    National Research Center for Haematology, Moscow 125167, Russia,Federal Research and Clinical Centre of Paediatric Haematology, Oncology and Immunology, Moscow 117198, Russia,M. V. Lomonosov Moscow State University, Moscow 119991, Russia,Center for Theoretical Problems of Physicochemical Pharmacology, Moscow 119991, Russia;

    Institute of Mechanical Engineering Problems, Saint Petersburg 199178, Russia;

    National Research Center for Haematology, Moscow 125167, Russia,Federal Research and Clinical Centre of Paediatric Haematology, Oncology and Immunology, Moscow 117198, Russia,M. V. Lomonosov Moscow State University, Moscow 119991, Russia,Center for Theoretical Problems of Physicochemical Pharmacology, Moscow 119991, Russia;

    National Research Center for Haematology, Moscow 125167, Russia,Federal Research and Clinical Centre of Paediatric Haematology, Oncology and Immunology, Moscow 117198, Russia;

    Institut Camille Jordan, UMR 5208 CNRS, University Lyon 1, 69622 Villeurbanne, France,INRIA Team Dracula, INRIA Antenne Lyon la Doua, 69603 Villeurbanne, France,European Institute of Systems Biology and Medicine, 69007 Lyon, France;

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