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Intestinal Stem Cell Isolation and Culture in a Porcine Model of Segmental Small Intestinal Ischemia
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Superoxide radicals in feline intestinal ischemia
Gastroenterology
|July 1, 1981
Summary
Superoxide radicals, not histamine or prostaglandins, significantly increase intestinal capillary permeability during ischemia. Superoxide dismutase (SOD) treatment protected against this ischemic damage.
Area of Science:
- Gastroenterology
- Physiology
- Vascular Biology
Background:
- Regional ischemia increases intestinal capillary permeability.
- Humoral agents are implicated in the pathogenesis of ischemic bowel.
- Understanding these agents is crucial for treating ischemic conditions.
Purpose of the Study:
- To assess the role of local humoral agents in increasing capillary permeability during intestinal ischemia.
- To identify the primary mediators responsible for enhanced permeability in ischemic bowel.
Main Methods:
- Estimating capillary permeability using lymph-to-plasma protein ratio and lymph flow in autoperfused cat ileum segments.
- Administering specific antagonists: benadryl + cimetidine, indomethacin, methylprednisolone, and superoxide dismutase (SOD).
- Administering intravenous E. coli endotoxin to normotensive preparations.
Main Results:
- Benadryl + cimetidine, indomethacin, or methylprednisolone did not significantly alter ischemia-induced permeability.
- Superoxide dismutase (SOD) significantly attenuated the increase in capillary permeability.
- High doses of E. coli endotoxin increased intestinal capillary permeability.
Conclusions:
- Superoxide radicals are primarily responsible for increased capillary permeability in the ischemic bowel.
- Histamine, prostaglandins, and corticosteroids do not play a major role in this specific mechanism.
- Targeting superoxide radicals may offer a therapeutic strategy for ischemic bowel conditions.
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