Flow velocity-dependent regulation of microvascular resistance in vivo.
Ákos Koller, Gabor Kaley
Abstract
Ákos Koller, Gabor Kaley
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.
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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.
Key concepts: Arteriole, Microcirculation, Blood flow, Cremaster muscle, Hemodynamics, Shear stress, In vivo, Red blood cell