Suzuki Y, Tateishi N, Soutani M, Maeda N
Department of Physiology, School of Medicine, Ehime University Shigenobu, Japan.
Int J Microcirc Clin Exp. 1996 Jul-Aug;16(4):187-94. doi: 10.1159/000179172.
Flow behavior of erythrocytes in microvessels and glass capillaries with an inner diameter of 10-50 microns was compared in relation to erythrocyte deformation and erythrocyte aggregation. This study was focused on the formation of a marginal cell-free layer, and the thickness was determined using an image processor. Human erythrocytes were perfused through a part of microvascular networks isolated from rabbit mesentery and through glass capillaries. Erythrocyte deformability was modified by treating erythrocytes with diamide, diazene-dicarboxylic acid bis[N,N-dimethylamide], and erythrocyte aggregation was accelerated by adding dextran (with a molecular weight of 70,400) to the perfusion medium. The thickness of the cell-free layer increased with an increase of the inner diameter of flow channel, with lowering the hematocrit, and with increasing the flow velocity of erythrocytes, in both microvessels and glass capillaries. Furthermore, the thickness of cell-free layer decreased with decreasing erythrocyte deformability, while it increased with accelerating erythrocyte aggregation. However, the alteration of the cell-free layer in response to the changes of these hemorheological conditions was more sensitive in microvessels than in glass capillaries. The present study concludes that flow behavior of erythrocytes in microvessels is qualitatively similar to, but quantitatively different from those in glass capillaries, as far as evaluated by the change of the thickness of the marginal cell-free layer.
比较了红细胞在微血管和内径为10 - 50微米的玻璃毛细管中的流动行为,以及红细胞变形和红细胞聚集情况。本研究聚焦于边缘无细胞层的形成,并使用图像处理器测定其厚度。将人体红细胞灌注通过从兔肠系膜分离的部分微血管网络以及玻璃毛细管。通过用二酰胺、二氮烯二羧酸双[N,N - 二甲基酰胺]处理红细胞来改变红细胞变形性,并通过向灌注介质中添加右旋糖酐(分子量为70400)来加速红细胞聚集。在微血管和玻璃毛细管中,无细胞层的厚度均随着流动通道内径的增加、血细胞比容的降低以及红细胞流速的增加而增加。此外,无细胞层的厚度随着红细胞变形性的降低而减小,随着红细胞聚集的加速而增加。然而,微血管中无细胞层对这些血液流变学条件变化的响应比玻璃毛细管中更敏感。本研究得出结论,就通过边缘无细胞层厚度的变化来评估而言,红细胞在微血管中的流动行为在定性上与在玻璃毛细管中的相似,但在定量上不同。