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Three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks

Using a high‐fidelity, 3D computational model of blood flow in microvascular networks, we provide the full 3D distribution of wall shear stress (WSS), and its gradient (WSSG), and quantify the influence of red blood cells (RBCs) on WSS and WSSG. The deformation and flow dynamics of the individual RB...

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Autores principales: Balogh, Peter, Bagchi, Prosenjit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503071/
https://www.ncbi.nlm.nih.gov/pubmed/31062494
http://dx.doi.org/10.14814/phy2.14067
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author Balogh, Peter
Bagchi, Prosenjit
author_facet Balogh, Peter
Bagchi, Prosenjit
author_sort Balogh, Peter
collection PubMed
description Using a high‐fidelity, 3D computational model of blood flow in microvascular networks, we provide the full 3D distribution of wall shear stress (WSS), and its gradient (WSSG), and quantify the influence of red blood cells (RBCs) on WSS and WSSG. The deformation and flow dynamics of the individual RBCs are accurately resolved in the model, while physiologically realistic microvascular networks comprised of multiple bifurcations, convergences, and tortuous vessels are considered. A strong heterogeneity in WSS and WSSG is predicted across the networks, with the highest WSS occurring in precapillary bifurcations and capillary vessels. 3D variations of WSS and WSSG are shown to occur due to both network morphology and the influence of RBCs. The RBCs increase the WSS by as much as three times compared to that when no RBCs are present, and the highest increase is observed in venules. WSSG also increases significantly, and high WSSGs occur over wider regions in the presence of RBCs. In most vessels, the circumferential component of WSSG is observed to be greater than the axial component in the presence of RBCs, while the opposite trend is observed when RBCs are not considered. These results underscore the important role of RBCs on WSS and WSSG that cannot be predicted by widely used 1D models of network blood flow. Furthermore, the subendothelium‐scale variations of WSS and WSSG predicted by the present model have implications in terms of endothelial cell functions in the microvasculature.
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spelling pubmed-65030712019-05-10 Three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks Balogh, Peter Bagchi, Prosenjit Physiol Rep Original Research Using a high‐fidelity, 3D computational model of blood flow in microvascular networks, we provide the full 3D distribution of wall shear stress (WSS), and its gradient (WSSG), and quantify the influence of red blood cells (RBCs) on WSS and WSSG. The deformation and flow dynamics of the individual RBCs are accurately resolved in the model, while physiologically realistic microvascular networks comprised of multiple bifurcations, convergences, and tortuous vessels are considered. A strong heterogeneity in WSS and WSSG is predicted across the networks, with the highest WSS occurring in precapillary bifurcations and capillary vessels. 3D variations of WSS and WSSG are shown to occur due to both network morphology and the influence of RBCs. The RBCs increase the WSS by as much as three times compared to that when no RBCs are present, and the highest increase is observed in venules. WSSG also increases significantly, and high WSSGs occur over wider regions in the presence of RBCs. In most vessels, the circumferential component of WSSG is observed to be greater than the axial component in the presence of RBCs, while the opposite trend is observed when RBCs are not considered. These results underscore the important role of RBCs on WSS and WSSG that cannot be predicted by widely used 1D models of network blood flow. Furthermore, the subendothelium‐scale variations of WSS and WSSG predicted by the present model have implications in terms of endothelial cell functions in the microvasculature. John Wiley and Sons Inc. 2019-05-06 /pmc/articles/PMC6503071/ /pubmed/31062494 http://dx.doi.org/10.14814/phy2.14067 Text en © 2019 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Balogh, Peter
Bagchi, Prosenjit
Three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks
title Three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks
title_full Three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks
title_fullStr Three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks
title_full_unstemmed Three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks
title_short Three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks
title_sort three‐dimensional distribution of wall shear stress and its gradient in red cell‐resolved computational modeling of blood flow in in vivo‐like microvascular networks
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503071/
https://www.ncbi.nlm.nih.gov/pubmed/31062494
http://dx.doi.org/10.14814/phy2.14067
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