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Oxygen radicals: effects on intestinal vascular permeability
The American Journal of Physiology
|August 1, 1984
Summary
Oxygen free radicals significantly increase intestinal vascular permeability. Scavenging these radicals with superoxide dismutase or dimethylsulfoxide attenuated this effect, suggesting their role in ischemia-related damage.
Area of Science:
- Physiology
- Biochemistry
- Pathophysiology
Background:
- Oxygen-derived free radicals are implicated in vascular permeability changes during intestinal ischemia.
- Direct assessment of oxygen radical effects on intestinal vascular permeability is crucial.
Purpose of the Study:
- To directly evaluate the impact of oxygen free radicals on intestinal capillary permeability.
- To quantify the increase in vascular permeability induced by a specific oxygen radical-generating system.
Main Methods:
- Infusion of hypoxanthine-xanthine oxidase into feline ileal arteries to generate oxygen radicals.
- Estimation of osmotic reflection coefficient (sigma d) for plasma proteins using lymph-to-plasma protein ratio and lymph flow.
- Administration of free radical scavengers (superoxide dismutase, dimethylsulfoxide) to assess their protective effects.
Main Results:
- Hypoxanthine-xanthine oxidase infusion significantly reduced sigma d from 0.92 to 0.66, indicating increased intestinal vascular permeability.
- Superoxide dismutase (sigma d = 0.86) and dimethylsulfoxide (sigma d = 0.83) significantly attenuated the permeability increase.
- The observed increase in permeability was comparable to that seen after 1 hour of ischemia.
Conclusions:
- Oxygen-derived free radicals, generated by hypoxanthine-xanthine oxidase, markedly increase intestinal vascular permeability.
- Superoxide anion and hydroxyl radicals contribute to this oxygen radical-induced permeability increase.
- These findings highlight the role of oxygen radicals in the pathophysiology of intestinal ischemia.