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Macro- and microscale variables regulate stent haemodynamics, fibrin deposition and thrombomodulin expression

机译:宏观和微观变量调节支架的血流动力学,纤维蛋白沉积和血栓调节蛋白表达

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摘要

Drug eluting stents are associated with late stent thrombosis (LST), delayed healing and prolonged exposure of stent struts to blood flow. Using macroscale disturbed and undisturbed fluid flow waveforms, we numerically and experimentally determined the effects of microscale model strut geometries upon the generation of prothrombotic conditions that are mediated by flow perturbations. Rectangular cross-sectional stent strut geometries of varying heights and corresponding streamlined versions were studied in the presence of disturbed and undisturbed bulk fluid flow. Numerical simulations and particle flow visualization experiments demonstrated that the interaction of bulk fluid flow and stent struts regulated the generation, size and dynamics of the peristrut flow recirculation zones. In the absence of endothelial cells, deposition of thrombin-generated fibrin occurred primarily in the recirculation zones. When endothelium was present, peristrut expression of anticoagulant thrombomodulin (TM) was dependent on strut height and geometry. Thinner and streamlined strut geometries reduced peristrut flow recirculation zones decreasing prothrombotic fibrin deposition and increasing endothelial anticoagulant TM expression. The studies define physical and functional consequences of macro- and microscale variables that relate to thrombogenicity associated with the most current stent designs, and particularly to LST.
机译:药物洗脱支架与晚期支架血栓形成(LST),延迟愈合以及支架支杆长时间暴露于血流有关。使用宏观扰动和不受干扰的流体流动波形,我们在数值上和实验上确定了微观模型支杆几何形状对由流动扰动介导的血栓形成条件的影响。在存在扰动和不受干扰的大体积流体流的情况下,研究了不同高度的矩形横截面支架支杆几何形状和相应的流线型。数值模拟和颗粒流可视化实验表明,整体流体流和支架支杆的相互作用调节了支气管周流再循环区的产生,大小和动力学。在没有内皮细胞的情况下,凝血酶产生的血纤蛋白的沉积主要发生在再循环区域。当存在内皮时,抗凝血栓调节蛋白(TM)的支撑物周围表达取决于支撑物高度和几何形状。较薄且流线型的支撑杆几何形状减少了支撑杆周围的回流区域,从而减少了血栓前纤维蛋白的沉积并增加了内皮抗凝剂TM的表达。这些研究定义了宏观和微观变量的物理和功能后果,这些变量与与最新支架设计(尤其是LST)相关的血栓形成有关。

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