Gregory K, Basmadjian D
Department of Chemical Engineering and Applied Chemistry, University of Toronto, Ontario, Canada.
Ann Biomed Eng. 1994 Mar-Apr;22(2):184-93. doi: 10.1007/BF02390376.
This work analyzes, for the first time, the combined role of blood flow, protein transport and the reaction network of the contact phase up to the "common pathway" of the blood coagulation cascade. The model is comprised of a set of 20 dominant reactions with 11 components. Systems of ODEs reducible to 4 coupled equations describe rigorously the dynamic behavior, while systems of algebraic equations, reducible to a single polynomial equation, model the steady state concentrations of the coagulants. The analysis showed that there is never more than one stable steady state. This is in contrast to the analysis of common pathway that gives rise to multiple concentration states. It also revealed a general robustness of the system to changes in procoagulant concentrations, inhibition rates and most activation rate constants. The system is largely impervious to the level of activated Factor XII, given that a trace (non-zero) level is present. In contrast, the system displays a dual response to flow and surface activity: A change in either of these factors alone can promote, have no effect on, or (in the case of flow) impede the progress of coagulation, depending on the value of the other factor. Their effects must therefore be examined in unison. These results may help resolve contradictory findings attributed to one or the other factor alone.
这项工作首次分析了血流、蛋白质运输以及接触相反应网络直至血液凝固级联反应“共同途径”的综合作用。该模型由一组包含11个组分的20个主要反应组成。可简化为4个耦合方程的常微分方程组严格描述了动态行为,而可简化为单个多项式方程的代数方程组则模拟了凝血剂的稳态浓度。分析表明,稳定稳态从不超过一个。这与产生多种浓度状态的共同途径分析形成对比。它还揭示了该系统对促凝剂浓度、抑制率和大多数活化速率常数变化的普遍稳健性。鉴于存在微量(非零)水平的活化因子XII,该系统在很大程度上不受其水平的影响。相比之下,该系统对血流和表面活性表现出双重反应:单独改变这两个因素中的任何一个,都可能促进、不影响或(就血流而言)阻碍凝血进程,这取决于另一个因素的值。因此,必须综合考察它们的影响。这些结果可能有助于解决仅归因于某一个因素的相互矛盾的研究结果。