Carlson Brian E, Arciero Julia C, Secomb Timothy W
Biotechnology and Bioengineering Center, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Am J Physiol Heart Circ Physiol. 2008 Oct;295(4):H1572-9. doi: 10.1152/ajpheart.00262.2008. Epub 2008 Aug 22.
The autoregulation of blood flow, the maintenance of almost constant blood flow in the face of variations in arterial pressure, is characteristic of many tissue types. Here, contributions to the autoregulation of pressure-dependent, shear stress-dependent, and metabolic vasoactive responses are analyzed using a theoretical model. Seven segments, connected in series, represent classes of vessels: arteries, large arterioles, small arterioles, capillaries, small venules, large venules, and veins. The large and small arterioles respond actively to local changes in pressure and wall shear stress and to the downstream metabolic state communicated via conducted responses. All other segments are considered fixed resistances. The myogenic, shear-dependent, and metabolic responses of the arteriolar segments are represented by a theoretical model based on experimental data from isolated vessels. To assess autoregulation, the predicted flow at an arterial pressure of 130 mmHg is compared with that at 80 mmHg. If the degree of vascular smooth muscle activation is held constant at 0.5, there is a fivefold increase in blood flow. When myogenic variation of tone is included, flow increases by a factor of 1.66 over the same pressure range, indicating weak autoregulation. The inclusion of both myogenic and shear-dependent responses results in an increase in flow by a factor of 2.43. A further addition of the metabolic response produces strong autoregulation with flow increasing by a factor of 1.18 and gives results consistent with experimental observation. The model results indicate that the combined effects of myogenic and metabolic regulation overcome the vasodilatory effect of the shear response and lead to the autoregulation of blood flow.
血流的自动调节,即在面对动脉压变化时维持几乎恒定的血流,是许多组织类型的特征。在此,使用理论模型分析了压力依赖性、剪切应力依赖性和代谢性血管活性反应对自动调节的贡献。七个串联的节段代表血管类别:动脉、大动脉、小动脉、毛细血管、小静脉、大静脉和静脉。大动脉和小动脉对局部压力和壁剪切应力的变化以及通过传导反应传递的下游代谢状态做出积极反应。所有其他节段被视为固定阻力。小动脉节段的肌源性、剪切依赖性和代谢性反应由基于离体血管实验数据的理论模型表示。为了评估自动调节,将预测的动脉压为130 mmHg时的血流量与80 mmHg时的血流量进行比较。如果血管平滑肌激活程度保持在0.5不变,则血流量增加五倍。当纳入张力的肌源性变化时,在相同压力范围内血流量增加1.66倍,表明自动调节较弱。同时纳入肌源性和剪切依赖性反应会使血流量增加2.43倍。进一步加入代谢性反应会产生强大的自动调节,血流量增加1.18倍,并且结果与实验观察一致。模型结果表明,肌源性和代谢性调节的联合作用克服了剪切反应的血管舒张作用,并导致了血流的自动调节。