Disruption of the venular endothelium significantly attenuated functional arteriolar vasodilation from 91 +/- 2 microns to 82 +/- 3 microns (P<0.01) in hamster cremaster muscle.
Absolute Event Rate: 82% vs 91%
p-value: p=<0.01
This study was designed to determine the importance of the venular endothelium in the vasodilation of adjacent arterioles during functional hyperemia. The hamster cremaster muscle was prepared for in vivo microscopy. Two silver-silver chloride electrodes were placed across the pedicle of the cremaster muscle, and a square-wave pulse (10 V amplitude, 1 ms duration, and 1 Hz frequency) was used to elicit muscle contraction. Muscle stimulation for 1 min resulted in a vasodilation of the first-order arterioles from 74 +/- 2 to 91 +/- 2 microns (n = 9, P < 0.05). After perfusion of the venule with air to disrupt the venular endothelium, there was no significant effect on the resting diameter, 73 +/- 3 microns, but the vasodilation associated with the muscle stimulation was significantly attenuated to 82 +/- 3 microns (P < 0.01). After completion of these experiments, the disruption of venular endothelium was confirmed by electron microscopy. The functional vasodilation of arterioles adjacent to venules with an intact endothelium (venules in which air did not enter) was retained after air perfusion (n = 6). These results suggest that the presence of the venular endothelium is important for the arteriolar vasodilation during functional hyperemia. We propose that the venular endothelium releases a relaxing factor responsible for a portion of the functional arteriolar vasodilation.
Saito et al. (Thu,) conducted a other in Functional hyperemia (n=15). Disruption of venular endothelium via air perfusion vs. Intact venular endothelium was evaluated on Vasodilation of first-order arterioles (diameter in microns) (p=<0.01). Disruption of the venular endothelium significantly attenuated functional arteriolar vasodilation from 91 +/- 2 microns to 82 +/- 3 microns (P<0.01) in hamster cremaster muscle.