Key Structural Features of Microvascular Networks Leading to the Formation of Multiple Equilibria

Journal article

We analyse mathematical models of blood flow in two simple vascular networks in order to identify structural features that lead to the formation of multiple equilibria. Our models are based on existing rules for blood rheology and haematocrit splitting. By performing bifurcation analysis on these simple network flow models, we identify a link between the changing flow direction in key vessels and the existence of multiple equilibria. We refer to these key vessels as redundant vessels, and relate the maximum number of equilibria with the number of redundant vessels. We vary geometric parameters of the two networks, such as vessel length ratios and vessel diameters, to demonstrate that equilibria are uniquely defined by the flow in the redundant vessels. Equilibria typically emerge in sets of three, each having a different flow characteristic in one of the network's redundant vessels. For one of the three equilibria, the flow within the relevant redundant vessel will be smaller in magnitude than the other two and the redundant vessel will contain few Red Blood Cells (RBCs), if any. For the other two equilibria, the redundant vessel contains RBCs and significant flow in the two available directions. These structural features of networks provide a useful geometric property when studying the equilibria of blood flow in microvascular networks.

Authors: Atkinson, G; Ben-Ami, Y; Maini, P; Pitt-Francis, J; Byrne, H

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Springer
• Journal: Bulletin of Mathematical Biology
• Volume: 87
• Issue: 2
• Pages: 30
• Publication date: 2025-01-23
• DOI: 10.1007/s11538-024-01404-y
• EISSN: 1522-9602
• ISSN: 0092-8240
• Pmid: 39847152
• Language: English
• Keywords: Humans; Multiple Equilibria; Hematocrit; Mathematical Concepts; Erythrocytes; Hemorheology; Microvascular Blood Flow; Models, Cardiovascular; Microvessels; Network Redundancy; Computer Simulation; Blood Flow Velocity; Animals; Microcirculation