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Article type: Research Article
Authors: Kiesewetter, H. | Dauer, U. | Teitel, P. | Schmid-Schönbein, H. | Trapp, R.
Affiliations: Abteilung Physiologie der RWTH Aachen, Schneebergweg 211, D-5100 Aachen, W.-Germany
Note: [] Accepted by: Guest Editors N. Ohshima and D.E. Brooks
Abstract: The SER allows the “deformability” of individual red blood cells to be quantitated by determining their passage time through a pore (d=5.8 μm, 1 =50 μm) under the shear stresses of 1.5 Pa-4 Pa. Using this system, we examined the influence of: 1. cytoplasmic viscosity, 2. membrane viscoelastic properties, 3. area to volume relationship. To change these determinants of RBC-deformability, the cells have been altered with 1. Acetylphenylhydrazine (0.016 mol/l), 2.diamide (0.5 mmol/l), 3. osmotic swelling (200 mosm/l) and osmotic shrinking (480 mosm/l) by suspending the cells in hypo- and hypertonic saline. The passage time has been found to be primarily influenced by changes in cytoplasmic viscosity. The same cells when tested in 4 other systems considered to measure RBC-deformability (filtrometer, packed cell viscometry, rheoscope and ektacytometry) behaved differently.
Keywords: RBC-Deformability, Single-Erythrocyte-Rigidometer, Constant Shear Stress Viscometer, Constant Shear Stress Viscometer, Polymicroviscometer, Rheoscope-Ektacytometer
DOI: 10.3233/BIR-1982-19610
Journal: Biorheology, vol. 19, no. 6, pp. 737-753, 1982
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