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Fractal Properties of Perfusion Heterogeneity in Optimized Arterial Trees: A Model Study

Regional blood flows in the heart muscle are remarkably heterogeneous. It is very likely that the most important factor for this heterogeneity is the metabolic need of the tissue rather than flow dispersion by the branching network of the coronary vasculature. To model the contribution of tissue nee...

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Autores principales: Karch, Rudolf, Neumann, Friederike, Podesser, Bruno K., Neumann, Martin, Szawlowski, Paul, Schreiner, Wolfgang
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234485/
https://www.ncbi.nlm.nih.gov/pubmed/12913088
http://dx.doi.org/10.1085/jgp.200208747
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author Karch, Rudolf
Neumann, Friederike
Podesser, Bruno K.
Neumann, Martin
Szawlowski, Paul
Schreiner, Wolfgang
author_facet Karch, Rudolf
Neumann, Friederike
Podesser, Bruno K.
Neumann, Martin
Szawlowski, Paul
Schreiner, Wolfgang
author_sort Karch, Rudolf
collection PubMed
description Regional blood flows in the heart muscle are remarkably heterogeneous. It is very likely that the most important factor for this heterogeneity is the metabolic need of the tissue rather than flow dispersion by the branching network of the coronary vasculature. To model the contribution of tissue needs to the observed flow heterogeneities we use arterial trees generated on the computer by constrained constructive optimization. This method allows to prescribe terminal flows as independent boundary conditions, rather than obtaining these flows by the dispersive effects of the tree structure. We study two specific cases: equal terminal flows (model 1) and terminal flows set proportional to the volumes of Voronoi polyhedra used as a model for blood supply regions of terminal segments (model 2). Model 1 predicts, depending on the number N (term) of end-points, fractal dimensions D of perfusion heterogeneities in the range 1.20 to 1.40 and positively correlated nearest-neighbor regional flows, in good agreement with experimental data of the normal heart. Although model 2 yields reasonable terminal flows well approximated by a lognormal distribution, it fails to predict D and nearest-neighbor correlation coefficients r (1) of regional flows under normal physiologic conditions: model 2 gives D = 1.69 ± 0.02 and r (1) = −0.18 ± 0.03 (n = 5), independent of N (term) and consistent with experimental data observed under coronary stenosis and under the reduction of coronary perfusion pressure. In conclusion, flow heterogeneity can be modeled by terminal positions compatible with an existing tree structure without resorting to the flow-dispersive effects of a specific branching tree model to assign terminal flows.
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spelling pubmed-22344852008-04-16 Fractal Properties of Perfusion Heterogeneity in Optimized Arterial Trees: A Model Study Karch, Rudolf Neumann, Friederike Podesser, Bruno K. Neumann, Martin Szawlowski, Paul Schreiner, Wolfgang J Gen Physiol Article Regional blood flows in the heart muscle are remarkably heterogeneous. It is very likely that the most important factor for this heterogeneity is the metabolic need of the tissue rather than flow dispersion by the branching network of the coronary vasculature. To model the contribution of tissue needs to the observed flow heterogeneities we use arterial trees generated on the computer by constrained constructive optimization. This method allows to prescribe terminal flows as independent boundary conditions, rather than obtaining these flows by the dispersive effects of the tree structure. We study two specific cases: equal terminal flows (model 1) and terminal flows set proportional to the volumes of Voronoi polyhedra used as a model for blood supply regions of terminal segments (model 2). Model 1 predicts, depending on the number N (term) of end-points, fractal dimensions D of perfusion heterogeneities in the range 1.20 to 1.40 and positively correlated nearest-neighbor regional flows, in good agreement with experimental data of the normal heart. Although model 2 yields reasonable terminal flows well approximated by a lognormal distribution, it fails to predict D and nearest-neighbor correlation coefficients r (1) of regional flows under normal physiologic conditions: model 2 gives D = 1.69 ± 0.02 and r (1) = −0.18 ± 0.03 (n = 5), independent of N (term) and consistent with experimental data observed under coronary stenosis and under the reduction of coronary perfusion pressure. In conclusion, flow heterogeneity can be modeled by terminal positions compatible with an existing tree structure without resorting to the flow-dispersive effects of a specific branching tree model to assign terminal flows. The Rockefeller University Press 2003-09 /pmc/articles/PMC2234485/ /pubmed/12913088 http://dx.doi.org/10.1085/jgp.200208747 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Karch, Rudolf
Neumann, Friederike
Podesser, Bruno K.
Neumann, Martin
Szawlowski, Paul
Schreiner, Wolfgang
Fractal Properties of Perfusion Heterogeneity in Optimized Arterial Trees: A Model Study
title Fractal Properties of Perfusion Heterogeneity in Optimized Arterial Trees: A Model Study
title_full Fractal Properties of Perfusion Heterogeneity in Optimized Arterial Trees: A Model Study
title_fullStr Fractal Properties of Perfusion Heterogeneity in Optimized Arterial Trees: A Model Study
title_full_unstemmed Fractal Properties of Perfusion Heterogeneity in Optimized Arterial Trees: A Model Study
title_short Fractal Properties of Perfusion Heterogeneity in Optimized Arterial Trees: A Model Study
title_sort fractal properties of perfusion heterogeneity in optimized arterial trees: a model study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234485/
https://www.ncbi.nlm.nih.gov/pubmed/12913088
http://dx.doi.org/10.1085/jgp.200208747
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