Flow velocity-dependent regulation of microvascular resistance in vivo.

A Koller, G Kaley
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Abstract

In skeletal (cremaster) muscle of pentobarbital anesthetized rats we tested the hypothesis that blood flow-dependent regulation of vascular resistance exists in the microcirculation. During occlusion of an arteriole we found that the consequent increase in red blood cell (RBC) velocity in a proximal parallel arteriole was followed by a mean increase in diameter of 32 percent (mean control diameter: 21.5 +/- 0.5 microns) of the arteriole under study. The increase in arteriolar diameter always appeared with a delay (mean: 8.4 +/- 0.5 s) following the onset of changes in RBC velocity. Upon release of the occlusion RBC velocity decreased followed by a decline in diameter of the arteriole under study. Since the changes in arteriolar diameter during this experimental intervention cannot be explained on the basis of previously described blood flow-regulatory mechanisms in the microcirculation we conclude that changes in blood flow velocity (wall shear stress) per se induced the changes in arteriolar diameter. The existence of this phenomenon suggests a new, flow velocity-sensitive mechanism which can regulate - via changes in diameter - the supply and distribution of blood flow in the microcirculation in vivo.

体内微血管阻力的流速依赖性调节。
在戊巴比妥麻醉大鼠的骨骼肌中,我们验证了微循环中存在血流依赖性血管阻力调节的假设。在小动脉闭塞期间,我们发现,在近端平行小动脉中,红细胞(RBC)速度随之增加,所研究的小动脉直径平均增加32%(平均对照直径:21.5±0.5微米)。小动脉直径的增加总是在RBC流速变化开始后出现延迟(平均8.4±0.5 s)。在解除闭塞后,RBC流速下降,随后小动脉直径下降。由于实验干预期间小动脉直径的变化不能根据先前描述的微循环血流调节机制来解释,因此我们得出结论,血流速度(壁面剪切应力)本身的变化诱导了小动脉直径的变化。这种现象的存在提示了一种新的、流速敏感的机制,它可以通过直径的变化来调节体内微循环中血流的供应和分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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