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理论比较壁衍生和红细胞衍生的代谢流调节机制在异质微血管网络中。

Theoretical comparison of wall-derived and erythrocyte-derived mechanisms for metabolic flow regulation in heterogeneous microvascular networks.

机构信息

Department of Anesthesiology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Am J Physiol Heart Circ Physiol. 2012 May 15;302(10):H1945-52. doi: 10.1152/ajpheart.01176.2011. Epub 2012 Mar 9.

Abstract

The objective of this study is to compare the effectiveness of metabolic signals derived from erythrocytes and derived from the vessel wall for regulating blood flow in heterogeneous microvascular networks. A theoretical model is used to simulate blood flow, mass transport, and vascular responses. The model accounts for myogenic, shear-dependent, and metabolic flow regulation. Metabolic signals are assumed to be propagated upstream along vessel walls via a conducted response. Arteriolar tone is assumed to depend on the conducted metabolic signal as well as local wall shear stress and wall tension, and arteriolar diameters are calculated based on vascular smooth muscle mechanics. The model shows that under certain conditions metabolic regulation based on wall-derived signals can be more effective in matching perfusion to local oxygen demand relative to regulation based on erythrocyte-derived signals, resulting in higher extraction and lower oxygen deficit. The lower effectiveness of the erythrocyte-derived signal is shown to result in part from the unequal partition of hematocrit at diverging bifurcations, such that low-flow vessels tend to receive a reduced hematocrit and thereby experience a reduced erythrocyte-derived metabolic signal. The model simulations predict that metabolic signals independent of erythrocytes may play an important role in local metabolic regulation of vascular tone and flow distribution in heterogeneous microvessel networks.

摘要

本研究旨在比较源自红细胞和血管壁的代谢信号在调节异质微血管网络中的血流的有效性。使用理论模型来模拟血流、质量传递和血管反应。该模型考虑了肌源性、剪切依赖性和代谢流量调节。假设代谢信号通过传导反应沿血管壁向上游传播。动脉张力取决于传导代谢信号以及局部壁切应力和壁张力,并且根据血管平滑肌力学计算出动脉直径。该模型表明,在某些条件下,基于壁衍生信号的代谢调节相对于基于红细胞衍生信号的调节,在匹配局部氧需求的灌注方面可能更有效,从而导致更高的提取和更低的氧缺乏。红细胞衍生信号的低效率部分是由于在发散分支处的血细胞比容分布不均匀,使得低流量血管倾向于接收较低的血细胞比容,从而经历较低的红细胞衍生代谢信号。模型模拟预测,独立于红细胞的代谢信号可能在异质微血管网络中血管张力和血流分布的局部代谢调节中发挥重要作用。

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