Dydek E Victoria, Chaikof Elliot L
Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, 110 Francis St, Suite 9F, Boston, MA, 02115, USA.
Wyss Institute of Biologically Inspired Engineering of Harvard University, Boston, MA, 02215, USA.
Ann Biomed Eng. 2016 Apr;44(4):1072-84. doi: 10.1007/s10439-015-1377-5. Epub 2015 Jul 14.
An expanded computational model of surface induced thrombin generation was developed that includes hemodynamic effects, 22 biochemical reactions and 44 distinct chemical species. Surface binding of factors V, VIII, IX, and X was included in order to more accurately simulate the formation of the surface complexes tenase and prothrombinase. In order to model these reactions, the non-activated, activated and inactivated forms were all considered. This model was used to investigate the impact of surface bound heparin on thrombin generation with and without the additive effects of thrombomodulin (TM). In total, 104 heparin/TM pairings were evaluated (52 under venous conditions, 52 under arterial conditions), the results demonstrating the synergistic ability of heparin and TM to reduce thrombin generation. Additionally, the role of circulating tissue factor (TF(p)) was investigated and compared to that of surface-bound tissue factor (TF(s)). The numerical results suggest that circulating TF has the power to amplify thrombin generation once the coagulation cascade is already initiated by surface-bound TF. TF(p) concentrations as low as 0.01 nM were found to have a significant impact on total thrombin generation.
开发了一种扩展的表面诱导凝血酶生成计算模型,该模型包括血流动力学效应、22种生化反应和44种不同的化学物质。为了更准确地模拟表面复合物凝血酶原酶和凝血酶原激活物的形成,纳入了因子V、VIII、IX和X的表面结合。为了对这些反应进行建模,考虑了非活化、活化和失活形式。该模型用于研究表面结合肝素在有和没有血栓调节蛋白(TM)附加作用的情况下对凝血酶生成的影响。总共评估了104种肝素/TM配对(静脉条件下52种,动脉条件下52种),结果表明肝素和TM具有协同降低凝血酶生成的能力。此外,研究了循环组织因子(TF(p))的作用,并与表面结合组织因子(TF(s))的作用进行了比较。数值结果表明,一旦凝血级联反应已由表面结合的TF启动,循环TF就有能力放大凝血酶生成。发现低至0.01 nM的TF(p)浓度对总凝血酶生成有显著影响。