Department of Mathematics and Statistics, Metropolitan State University of Denver, Denver, CO, USA.
Department of Physiology, University of Arizona, Tucson, AZ, USA.
Microcirculation. 2021 Jul;28(5):e12690. doi: 10.1111/micc.12690. Epub 2021 Mar 18.
A theoretical model is used to analyze combinations of RBC-derived and wall-derived (RBC-independent) mechanisms for metabolic blood flow regulation, with regard to their oxygen transport properties.
Heterogeneous microvascular network structures are derived from observations in rat mesentery and hamster cremaster. The effectiveness of metabolic blood flow regulation using combinations of RBC-dependent and RBC-independent mechanisms is simulated in these networks under conditions of reduced oxygen delivery and increased oxygen demand.
Metabolic regulation by a wall-derived mechanism results in higher predicted total blood flow rate and number of flowing vessels, and lower tissue hypoxic fraction, than regulation by combinations of RBC-derived and wall-derived signals. However, a combination of RBC-derived and wall-derived signals results in a higher predicted median tissue P than either mechanism acting alone.
Model results suggest complementary roles for RBC-derived and wall-derived mechanisms of metabolic flow regulation, with the wall-derived mechanism responsible for avoiding hypoxia, and the RBC-derived mechanism responsible for maintaining P levels high enough for optimal tissue function.
利用理论模型分析 RBC 衍生和壁衍生(RBC 独立)机制的组合,以研究其氧输送特性对代谢性血流调节的影响。
从大鼠肠系膜和仓鼠提睾肌的观察中得出异质微血管网络结构。在低氧输送和高氧需求条件下,模拟这些网络中 RBC 依赖和 RBC 独立机制组合对代谢性血流调节的有效性。
与 RBC 衍生和壁衍生信号组合调节相比,壁衍生机制导致更高的预测总血流速率和流动血管数量,以及更低的组织缺氧分数。然而,RBC 衍生和壁衍生信号的组合导致更高的预测中位数组织 P 值,高于任一机制单独作用。
模型结果表明 RBC 衍生和壁衍生代谢性血流调节机制具有互补作用,壁衍生机制负责避免缺氧,而 RBC 衍生机制负责维持足够高的 P 值以实现最佳组织功能。