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Department of Physiology, Freie Universität Berlin, D-14195 Berlin, Germany
Blood flow in
microvessels differs significantly from that of red blood cells (RBC)
flowing through long, straight glass tubes in vitro. The in vivo
situation is characterized by the presence of plasma favoring
aggregation, by the irregular geometry of vessel segments, and by
frequent branching points. Here, a method is presented to characterize
flow patterns in microvascular blood flow during intravital microscopy
based on Fourier analysis of recorded light intensity patterns. The
interpretation of the resulting power spectra in terms of pattern size
distribution was validated by model experiments employing artificial
textures and by reverse transformation of idealized spectra. The
determined size of RBC flow patterns in microvessels ranged from ~8
µm in capillaries to ~14 µm in vessels of >30 µm. With
increasing shear rate above ~100 s
1 pattern size
increased, possibly reflecting formation of short-lived flow clusters.
Below ~100 s
1 an increase of pattern size with
decreasing shear rate was found in experiments using local occlusion
and treatment with high-molecular-weight dextran, suggesting the
formation of aggregates. The dynamic process of generation and
destruction of RBC flow patterns could well contribute to flow
resistance in vivo in peripheral vascular beds.
Fourier analysis; aggregation; hemodynamics; shear rate
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