Reid Heart Center/FirstHealth of Carolinas Cardiac and Vascular Institute, Pinehurst, NC, USA.
Department of Physics, Naval Postgraduate School, Monterey, CA, USA.
Platelets. 2020;31(3):373-382. doi: 10.1080/09537104.2019.1636021. Epub 2019 Jul 17.
Platelets are central to thrombosis. However, it is unknown whether platelets slip at vascular or device surfaces. The presence of platelet slip at a surface would interrupt physical contact between the platelet and that surface, and therefore diminish adhesion and thrombosis. Unfortunately, no existing technology can directly measure platelet slip in a biological environment. The objective of this study was to explore whether microspheres-modeling platelets-slip at different vascular and device surfaces in an acrylic scaled-up model coronary artery. The microspheres (3.12 µm diameter) were suspended in a transparent glycerol/water experimental fluid, which flowed continuously at Reynolds numbers typical of coronary flow (200-400) through the model artery. We placed a series of axisymmetric acrylic stenoses (cross-sectional area reduction [CSAr], 20-90%) into the model artery, both without and with a central cylinder present (modeling a percutaneous interventional guide wire, and with a scaled-up Doppler catheter mounted upstream). We used laser Doppler velocimetry (LDV) to measure microsphere velocities within, proximal and distal to each stenosis, and compared to computer simulations of fluid flow with no-slip. For validation, we replaced the acrylic with paraffin stenoses (more biologically relevant from a surface roughness perspective) and then analyzed the signal recorded by the scaled-up Doppler catheter. Using the LDV, we identified progressive microsphere slip proportional to CSAr inside entrances for stenoses ≥60% and ≥40% without and with cylinder present, respectively. Additionally, microsphere slip occurred universally along the cylinder surface. Computer simulations indicated increased fluid shear rates (velocity gradients) at these particular locations, and logistic regression analysis comparing microsphere slip with fluid shear rate resulted in a c-index of 0.989 at a cut-point fluid shear rate of (10.61 [cm]×mean velocity [cm×sec]). Moreover, the presence of the cylinder caused disordering of microsphere shear rates distal to higher grade stenoses, indicating a disturbance in their flow. Finally, despite lower precision, the signal recorded by the scaled-up Doppler catheter nonetheless indicated slip at the entry into and at most locations distal to the 90% stenosis. Our validated model establishes proof of concept for platelet slip, and platelet slip explains several important basic and clinical observations. If technological advances allow confirmation in a true biologic environment, then our results will likely influence the development of shear-dependent antiplatelet drugs. Also, adding shear rate information, our results provide a direct experimental fluid dynamic foundation for antiplatelet-focused antithrombotic therapy during coronary interventions directed towards higher grade atherosclerotic stenoses.
血小板在血栓形成中起着核心作用。然而,目前尚不清楚血小板是否会在血管或器械表面滑动。如果血小板在表面滑动,将会中断血小板与表面之间的物理接触,从而减少粘附和血栓形成。不幸的是,目前还没有技术可以直接在生物环境中测量血小板的滑动。本研究的目的是探索微球(模拟血小板)是否会在模拟冠状动脉的丙烯 scaled-up 模型中在不同的血管和器械表面发生滑动。微球(直径 3.12 µm)悬浮在透明甘油/水实验流体中,该流体以典型的冠状动脉流动雷诺数(200-400)连续流过模型动脉。我们将一系列轴对称丙烯狭窄(截面积减少[CSAr],20-90%)放置在模型动脉中,既没有也没有中央圆柱(模拟经皮介入导丝,并且上游安装了放大多普勒导管)。我们使用激光多普勒测速仪(LDV)测量每个狭窄处近端和远端微球的速度,并将其与无滑移的流体流动计算机模拟进行比较。为了验证,我们用石蜡狭窄(从表面粗糙度的角度来看更具生物学意义)代替丙烯狭窄,然后分析放大多普勒导管记录的信号。使用 LDV,我们确定在入口处,随着狭窄程度≥60%和≥40%(无和有圆柱),微球的滑动逐渐增加。此外,微球的滑动普遍发生在圆柱表面上。计算机模拟表明,在这些特定位置的流体剪切率(速度梯度)增加,并且比较微球滑动与流体剪切率的逻辑回归分析导致在剪切率为(10.61 [cm]×平均速度[cm×sec])的剪切率处的 c 指数为 0.989。此外,圆柱的存在导致较高等级狭窄处下游微球剪切率的紊乱,表明其流动受到干扰。最后,尽管精度较低,但放大多普勒导管记录的信号仍表明在 90%狭窄的入口处以及大多数远端位置发生了滑动。我们验证的模型为血小板滑动提供了概念验证,如果技术进步可以在真正的生物环境中得到确认,那么我们的结果可能会影响依赖于剪切的抗血小板药物的开发。此外,通过添加剪切率信息,我们的结果为针对较高等级动脉粥样硬化狭窄的冠状动脉介入治疗中抗血小板聚焦抗血栓治疗提供了直接的实验流体动力学基础。