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

• Published in: Physiological reports Vol. 7; no. 9; pp. e14067 - n/a
• Main Authors: Balogh, Peter, Bagchi, Prosenjit
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01-05-2019; John Wiley and Sons Inc
• Subjects: Blood flow; Blood Flow Velocity - physiology; Cell adhesion & migration; Cellular Physiology; Computational modeling; Computer applications; Computer Simulation; Endothelial cells; Erythrocytes; Erythrocytes - physiology; Hemorheology - physiology; Humans; Microcirculation; Microcirculation - physiology; microvascular networks; Microvasculature; Microvessels - physiology; Models, Cardiovascular; Morphology; Original Research; Physiology; red blood cells; Regional Blood Flow - physiology; Shear stress; Stress, Mechanical; Studies; Vasculature; Velocity; wall shear stress; red blood cells; Computational modeling; microvascular networks; microcirculation; wall shear stress
• ISSN: 2051-817X; 2051-817X
• DOI: 10.14814/phy2.14067

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.
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.