A two-layer continuously distributed capillary O₂ transport model applied to blood flow regulation in resting...

The microcirculation is the site of direct oxygen (O₂) transfer from blood to tissue, and also of O₂ delivery control via regulation of local blood flow. In addition, a number of diseases including type II diabetes mellitus (DMII) and sepsis are known to produce microcirculatory dysfunction in their early phases. Given the complexity of microvascular structure and physiology, and the difficulty of measuring tissue oxygenation at the micro-scale, mathematical modelling has been necessary for understanding the physiology and pathophysiology of O₂ transport in the microcirculation and for interpreting in vivo experiments. To advance this area, a model of blood-tissue O₂ transport in skeletal muscle was recently developed which uses continuously distributed capillaries and includes O₂ diffusion, convection, and consumption. The present work extends this model to two adjacent layers of skeletal muscle with different blood flow rates and applies it to study steady-state O₂ transport when flow regulation is stimulated using an O₂ exchange chamber. To generate a model which may be validated through in vivo experiments, an overlying O₂ permeable membrane is included. The model is solved using traditional methods including separation of variables and Fourier decomposition, and to ensure smooth profiles at the muscle-muscle and muscle-membrane interfaces, matching conditions are developed. The study presents qualitative verification for the model, using visualizations of tissue O₂ pressure (PO₂) distributions for varying capillary density (CD), and presents capillary velocity response values in the near layer for varying chamber PO₂ under the assumption that outlet capillary O₂ saturation (SO₂) is equalized between adjacent layers. These compensatory velocity profiles, along with effective 'no-flux' chamber PO₂ values, are presented for varying CD and tissue O₂ consumption values. Insights gained from the two-layer model provide guidance for interpreting and planning future in vivo experiments, and also provide motivation for further development of the model to improve understanding of the interaction between O₂ transport and blood flow regulation.