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. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: Ann Biomed Eng. 2012 Aug 23;40(11):2379–2398. doi: 10.1007/s10439-012-0613-5

Figure 7.

Figure 7

Schematic diagram of a four-region, axially distributed, blood–tissue exchange (BTEX) model for advection, diffusion, permeation, reaction, and binding of oxygen (O2), carbon dioxide (CO2), bicarbonate (HCO3), and hydrogen ions (H+) in the heart. Endothelial cells region in the capillary membrane were ignored. Detailed kinetics of the binding of O2 and CO2 to hemoglobin (Hb) in blood (nonlinear O2-CO2 interactions) and the binding of O2 to myoglobin (Mb) in the parenchymal cells were considered. For the four species, there are four four-region models in parallel. Consumption of O2 and production of CO2 occurred only in the parenchymal cells, ignoring O2 utilization elsewhere. Detailed cellular metabolism leading to consumption of O2 and production of CO2 was ignored. The rates of CO2 production and O2 consumption were phenomenologically related to respiratory quotient (RQ) which was set 1.0 for glucose metabolism, 0.8 for fat metabolism, and 0.7 for protein metabolism, averaging about 0.8 in normal physiological conditions. F denotes blood flow, V denotes anatomical volumes, V′ denotes the effective water spaces (including binding spaces), PS denotes permeability surface area product, D denotes the effective axial diffusion (dispersion), and G denotes the rate of O2 consumption and CO2 production; rbc: red blood cells, pl: plasma, isf: interstitial fluid, pc: parenchymal cells. (The figure is taken from Dash and Bassingthwaighte44 with permission.)