Structural adaptation and stability of microvascular networks: theory and simulations
1 Deutsches Herzzentrum Berlin, D-13353 Berlin, Germany; 2 Department of Physiology, University of Arizona, Tucson, Arizona 85724; and 3 Department of Physiology, Freie Universität Berlin, D-14195 Berlin, Germany A theoretical model was developed to simulate long-term changes of vessel diameters...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 1998-08, Vol.275 (2), p.H349-H360 |
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Sprache: | eng |
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Zusammenfassung: | 1 Deutsches Herzzentrum Berlin,
D-13353 Berlin, Germany;
2 Department of Physiology,
University of Arizona, Tucson, Arizona 85724; and
3 Department of Physiology,
Freie Universität Berlin, D-14195 Berlin, Germany
A theoretical
model was developed to simulate long-term changes of vessel diameters
during structural adaptation of microvascular networks in response to
tissue needs. The diameter of each vascular segment was assumed to
change with time in response to four local stimuli: endothelial wall
shear stress ( w ),
intravascular pressure (P), a flow-dependent metabolic stimulus (M),
and a stimulus conducted from distal to proximal segments along
vascular walls (C). Increases in
w , M, or C or decreases in P
were assumed to stimulate diameter increases. Hemodynamic quantities
were estimated using a mathematical model of network flow. Simulations
were continued until equilibrium states were reached in which the
stimuli were in balance. Predictions were compared with data from
intravital microscopy of the rat mesentery, including topological
position, diameter, length, and flow velocity for each segment of
complete networks. Stable equilibrium states, with realistic
distributions of velocities and diameters, were achieved only when all
four stimuli were included. According to the model, responses to
w and P ensure that diameters
are smaller in peripheral than in proximal segments and are larger in
venules than in corresponding arterioles, whereas M prevents collapse
of networks to single pathways and C suppresses generation of large
proximal shunts.
shear stress; pressure; conducted response; mathematical modeling |
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ISSN: | 0363-6135 0002-9513 1522-1539 |
DOI: | 10.1152/ajpheart.1998.275.2.h349 |