Singh M, Kumaravel M
Biomedical Engineering Division, Indian Institute of Technology, Madras, India.
Indian J Biochem Biophys. 1996 Jun;33(3):199-205.
Aggregation mechanism and deformability in pentoxifylline- and dispirin-treated erythrocytes are measured and compared with that of normal cells. The aggregation process is analyzed in terms of parameters which are obtained from the sequential recording of the transmitted light signal throughout the aggregate formation and sedimentation process. Erythrocyte deformability is determined by measurement of passage time through cellulose membrane. The variations in aggregation parameters in pentoxifylline-treated samples show that the formed aggregates are of larger size which sediment faster. In dispirin-treated cells, the formation of large size aggregates is delayed. The entire process is completed faster in pentoxifylline-treated compared to that of dispirin-treated cell whereas the normal sample shows an intermediate value. The deformability of erythrocytes treated with these drugs is increased.
测量并比较了己酮可可碱和双水杨酸酯处理的红细胞的聚集机制和变形性,并与正常细胞进行对比。根据在聚集体形成和沉降过程中透射光信号的连续记录所获得的参数来分析聚集过程。通过测量红细胞通过纤维素膜的时间来确定其变形性。己酮可可碱处理的样本中聚集参数的变化表明,形成的聚集体尺寸更大,沉降更快。在双水杨酸酯处理的细胞中,大尺寸聚集体的形成延迟。与双水杨酸酯处理的细胞相比,己酮可可碱处理的细胞整个过程完成得更快,而正常样本显示出中间值。用这些药物处理的红细胞的变形性增加。