Lima Rui, Ishikawa Takuji, Imai Yohsuke, Takeda Motohiro, Wada Shigeo, Yamaguchi Takami
Department of Bioengineering and Robotics, Graduate School of Engineering, Tohoku University, 6-6-01 Aoba, 980-8579 Sendai, Miagi, Japan.
J Biomech. 2008 Jul 19;41(10):2188-96. doi: 10.1016/j.jbiomech.2008.04.033. Epub 2008 Jun 26.
The flow properties of blood in the microcirculation depend strongly on the hematocrit (Hct), microvessel geometry, and cell properties. Previous in vitro studies have measured the radial displacement of red blood cells (RBCs) at concentrated suspensions using conventional microscopes. However, to measure the RBCs motion they used transparent suspensions of ghost red cells, which may have different physical properties than normal RBCs. The present study introduces a new approach (confocal micro-PTV) to measure the motion of labeled RBCs flowing in concentrated suspensions of normal RBCs. The ability of confocal systems to obtain thin in-focus planes allowed us to measure the radial position of individual RBCs accurately and to consequently measure the interaction between multiple labeled RBCs. All the measurements were performed in the center plane of both 50 and 100 microm glass capillaries at Reynolds numbers (Re) from 0.003 to 0.005 using Hcts from 2% to 35%. To quantify the motion and interaction of multiple RBCs, we used the RBC radial dispersion (D(yy)). Our results clearly demonstrate that D(yy) strongly depends on the Hct. The RBCs exhibited higher D(yy) at radial positions between 0.4 and 0.8R and lower D(yy) at locations adjacent to the wall (0.8-1R) and around the middle of the capillary (0-0.2R). The present work also demonstrates that D(yy) tends to decrease with a decrease in the diameter. The information provided by this study not only complements previous investigations on microhemorheology of both dilute and concentrated suspensions of RBCs, but also shows the influence of both Hct and geometry on the radial dispersion of RBCs. This information is important for a better understanding of blood mass transport mechanisms under both physiological and pathological conditions.
微循环中血液的流动特性在很大程度上取决于血细胞比容(Hct)、微血管几何形状和细胞特性。以往的体外研究使用传统显微镜测量了浓缩悬浮液中红细胞(RBC)的径向位移。然而,为了测量RBC的运动,他们使用了幽灵红细胞的透明悬浮液,其物理性质可能与正常RBC不同。本研究引入了一种新方法(共聚焦显微粒子图像测速技术)来测量在正常RBC浓缩悬浮液中流动的标记RBC的运动。共聚焦系统获取薄聚焦平面的能力使我们能够准确测量单个RBC的径向位置,并因此测量多个标记RBC之间的相互作用。所有测量均在50和100微米玻璃毛细管的中心平面进行,雷诺数(Re)为0.003至0.005,血细胞比容为2%至35%。为了量化多个RBC的运动和相互作用,我们使用了RBC径向扩散系数(D(yy))。我们的结果清楚地表明,D(yy)在很大程度上取决于血细胞比容。RBC在径向位置0.4至0.8R处表现出较高的D(yy),而在靠近管壁(0.8 - 1R)和毛细管中部附近(0 - 0.2R)处表现出较低的D(yy)。本研究还表明,D(yy)倾向于随着直径的减小而降低。本研究提供的信息不仅补充了先前对RBC稀释和浓缩悬浮液微观血液流变学的研究,还展示了血细胞比容和几何形状对RBC径向扩散的影响。这些信息对于更好地理解生理和病理条件下的血液质量传输机制非常重要。