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A comparative study: perfusion of the micro- and macrocirculation as a function of the hematocrit value
G Driessen1, H Scheidt, W Inhoffen
1Department of Physiology, Faculty of Medicine, RWTH Aachen, Federal Republic of Germany.
Microvascular Research
|January 1, 1988
Summary
Red blood cell (RBC) fluidity in vivo closely matches macrocirculatory data and is higher than in vitro measurements. Fluidity decreases with higher hematocrit but is independent of driving pressure within a specific range.
Area of Science:
- Biophysics
- Physiology
- Microcirculation Research
Background:
- Understanding red blood cell (RBC) suspension fluidity is crucial for comprehending blood flow dynamics in microcirculation.
- In vivo measurements offer a more accurate representation of RBC behavior compared to in vitro methods.
Purpose of the Study:
- To compare in vivo and in vitro measurements of red blood cell (RBC) suspension fluidity.
- To investigate the influence of hematocrit, perfusion pressure, and aggregation on RBC fluidity in the microvasculature.
Main Methods:
- Utilized microcirculatory measurements (RBC velocity, micropressure, vessel geometry) and macrocirculatory data (volume flow, perfusion pressure) in isolated rat mesentery.
- Employed microscopy with a video TV system to record microcirculatory perfusion under varying conditions.
- Compared in vivo data with in vitro viscometry results using human RBCs in Ringer's or Ficoll solutions.
Main Results:
- In vivo microfluidities correlated strongly with macroflow-derived fluidities.
- RBC fluidity decreased with increasing hematocrit but was independent of driving pressure (4-10 kPa).
- In vivo fluidities were higher than in vitro measurements, particularly at higher hematocrit values and specific shear stresses.
Conclusions:
- Microcirculatory and macrocirculatory measurements provide consistent estimates of in vivo RBC fluidity.
- Factors like high hematocrit, low perfusion pressure, and increased RBC aggregability can lead to vessel stagnation.