Erythrocyte flow and elasticity of microvessels, evaluated by marginal cell-free layer and flow resistance . Maeda, Nobuji, Yoji Suzuki, Junya Tanaka, and Norihiko Tateishi. Department of Physiology, School of Medicine, Ehime University, Shigenobu, Onsen-gun, Ehime 791-02, Japan
APStracts 3:0247H, 1996.
Flow dynamics of human erythrocytes was compared in elastic (E-) and hardened (H-) microvessels with inner diameter of 10-40 um. The thickness of the marginal cell-free layer and the overall flow resistance were measured using a vascular bed (E-vascular bed) isolated from rabbit mesentery as well as a 4% paraformaldehyde-fixed bed (H-vascular bed). (i) In both E- and H-microvessels, the thickness of the cell-free layer increased with increasing inner diameter of the microvessels and with decreasing hematocrit accompanied by an overall decrease of the flow resistance. The hematocrit-dependent change of cell-free layer thickness was greater in the E-microvessels than in the H-microvessels. The flow resistance was always greater in the H-vascular beds than in the E-vascular beds. (ii) With decreasing erythrocyte deformability induced by treatment with 2 mM diazene-dicarboxylic acid bis[N,N-dimethylamide], the thickness of the cell-free layer decreased at a low hematocrit in the E-microvessels and at a high hematocrit in the H-microvessels, though the flow resistance increased in both vascular beds. (iii) Dextran of 70,400 avg mol wt accelerated the formation of the cell -free layer by inducing erythrocyte aggregation. A drastic increase of the cell-free layer thickness at 2-4 g/dl dextran in the E -microvessels and at 1-2 g/dl dextran in the H-microvessels was accompanied by a significantly lower increase of the flow resistance. This study concludes that elasticity of microvessels may play an important role for reducing the overall flow resistance of a vascular bed, which is modulated by the marginal cell-free layer, itself a function of the rheological properties of the erythrocytes.

Received 26 February 1996; accepted in final form 10 June 1996.
APS Manuscript Number H186-6.
Article publication pending Am. J. Physiol. (Heart Circ. Physiology).
ISSN 1080-4757 Copyright 1996 The American Physiological Society.
Published in APStracts on 28 June 96