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Updated: Aug 2, 2026

Murine Model of Intestinal Ischemia-reperfusion Injury
Published on: May 11, 2016
Alterations in intestinal permeability and blood flow in a new model of mesenteric ischemia
1Department of Surgery, University of Texas Health Science Center, Dallas 75235-9031.
Abstract:
Disturbances in intestinal circulation for even short periods of time can produce mucosal injury, translocation of gut bacteria, and multiple organ failure. We recently reported a model of intestinal ischemia that included occlusion of the superior mesenteric artery (SMA) and interruption of collateral arcades from the right colic and jejunal arteries for 20 min. This present study was designed to characterize further our model of intestinal ischemia by quantitatively assessing changes in intestinal permeability (plasma to luminal clearance of 51Cr-labeled EDTA) and intestinal blood flow (IBF) (microspheres). A total of 89 rats were included for study; mean arterial blood pressure and acid-base balance were not significantly altered by intestinal ischemia or reperfusion. Baseline measurements of 51Cr-labeled EDTA were not significantly different among the experimental animals, and clearance did not change throughout the experimental period in the sham-ischemic group (N = 14). Clearance of 51Cr-labeled EDTA at the end of 20 min of intestinal ischemia (0.194 +/- 0.057 ml/min/100 gm, N = 17) was significantly greater than that measured at control (0.079 +/- 0.006 ml/min/100 gm, P less than 0.05). In addition, clearance measurements during reperfusion (20 min, 0.362 +/- 0.051; 60 min, 0.267 +/- 0.084 ml/min/gm) were significantly higher than those measured at the end of ischemia. Baseline IBF was similar in all rats (N = 42); SMA occlusion reduced IBF by 99% from baseline (from 1.4 +/- 0.27 to 0.014 +/- 0.001 ml/min/gm, N = 20). Removal of the SMA clip returned intestinal perfusion to baseline values (1.72 +/- 0.51 ml/min/g).(ABSTRACT TRUNCATED AT 250 WORDS)
Insights
Intestinal ischemia significantly increases intestinal permeability, indicating damage to the gut barrier. Blood flow returns to normal after reperfusion, but permeability remains elevated, highlighting potential long-term risks.
Area of Science:
- Gastroenterology
- Physiology
- Surgical Research
Background:
- Intestinal ischemia can lead to mucosal injury, bacterial translocation, and organ failure.
- A validated rat model of intestinal ischemia involving superior mesenteric artery (SMA) occlusion was previously established.
Purpose of the Study:
- To quantitatively assess changes in intestinal permeability and intestinal blood flow (IBF) in a rat model of intestinal ischemia.
- Further characterize the physiological consequences of a 20-minute intestinal ischemia and reperfusion insult.
Main Methods:
- Utilized 89 rats, measuring plasma to luminal clearance of 51Cr-labeled EDTA to assess intestinal permeability.
- Employed microspheres to quantify intestinal blood flow (IBF) changes during ischemia and reperfusion.
- Monitored mean arterial blood pressure and acid-base balance throughout the experiment.
Main Results:
- Intestinal ischemia for 20 minutes significantly increased intestinal permeability compared to baseline controls (P < 0.05).
- Intestinal permeability remained significantly elevated during both early and later reperfusion periods.
- Superior mesenteric artery (SMA) occlusion reduced intestinal blood flow by 99%, with perfusion returning to baseline after reperfusion.
Conclusions:
- The established rat model effectively demonstrates increased intestinal permeability following ischemic insult.
- Elevated intestinal permeability post-reperfusion suggests a persistent disruption of the gut barrier.
- This model provides a valuable tool for studying the pathophysiology and potential therapeutic interventions for intestinal ischemia.
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