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Reactive oxygen species modify reflex cardiovascular responses to static contraction
S Bonigut1, C L Stebbins, J C Longhurst
1Department of Internal Medicine, University of California, Davis 95616, USA.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|September 1, 1996
Summary
Reactive oxygen species inhibit the exercise pressor reflex, contrary to their effect on visceral afferents. This suggests a complex role for free radicals in cardiovascular regulation during muscle activity.
Area of Science:
- Cardiovascular Physiology
- Exercise Physiology
- Free Radical Biology
Background:
- Reactive oxygen species (ROS) activate the cardiovascular system via visceral afferents, involving hydroxyl radicals.
- The role of ROS in the exercise pressor reflex, a cardiovascular response to muscle contraction, is not fully understood.
Purpose of the Study:
- To test the hypothesis that ROS contribute to the reflex cardiovascular response during static muscle contraction.
- To investigate the mechanism by which ROS influence the exercise pressor reflex.
Main Methods:
- Anesthetized cats underwent intermittent static contraction of triceps surae muscles.
- Cardiovascular responses (blood pressure, heart rate) were measured before and after administration of free radical scavengers (dimethylthiourea or deferoxamine).
- Popliteal artery blood velocity was assessed using Doppler flowmetry to evaluate local vasodilation.
Main Results:
- Administration of dimethylthiourea or deferoxamine augmented the contraction-induced pressor response.
- Heart rate responses to contraction were not significantly affected by the free radical scavengers.
- Deferoxamine did not alter blood velocity in the popliteal artery during contraction, indicating no effect on local vasodilation.
Conclusions:
- Reactive oxygen species exert an inhibitory effect on the exercise pressor reflex.
- This inhibitory effect is independent of ROS-mediated local vasodilation in skeletal muscle.
- The findings contrast with the known stimulatory effect of ROS on visceral afferents, highlighting differential roles in cardiovascular control.