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Updated: Feb 1, 2026

Assessment of Gut Barrier Integrity in Mice Using Fluorescein-Isothiocyanate-Labeled Dextran
Published on: November 18, 2022
Time-Dependent Alterations of Gut Wall Integrity in Small Bowel Obstruction in Mice
Lisa Hartmann1, Xue Zhao2, Till Macheroux2
1Department of Surgery, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany; Berlin Institute of Health (BIH), Berlin, Germany.
Background:
Small bowel obstruction (SBO) is one of the most common disorders in surgical emergency departments. Without resolution of the obstructed bowel segments, patients may develop multiorgan failure. The aim of this study was to investigate whether morphological damage of the intestinal wall during SBO may lead to molecular translocation and how this may impair intestinal motility.
Methods:
C57Bl6 mice were laparotomized, and the small intestine was ligated 5 cm oral to the coecum for SBO. Controls received minilaparotomy only. Animals were sacrificed 3 h, 9 h, and 24 h after SBO. Morphological changes were evaluated on hematoxylin and eosin histology by a standardized score. Intestinal motility was determined by recording intraluminal pressure of the small intestine in vitro. Permeability was measured by fluorospectroscopy and ELISA of blood samples after oral gavage with fluorescein isothiocyanate (FITC)-dextrane and horse radish peroxidase. Data are mean ± SD.
Results:
Three hours after SBO, FITC-dextrane uptake was increased to 187.6 ± 15.2 ng/mL compared to controls (P = 0.011). At 9 h, uptake of horse radish peroxidase (23.0 ± 8.6 ng/mL, 9.0 ± 6.3 ng/mL, P = 0.039) and FITC-dextrane (86.8 ± 17.8 ng/mL, 62.0 ± 1.6 ng/mL, P = 0.029) was higher compared to controls. Motility was increased to 162.2 ± 20.2 area under the curve (AUC) compared to 121.3 ± 20.3 AUC in controls, P = 0.009 and an increased histology score was observed at 9 h (3.2 ± 1.8 versus 0.6 ± 0.7, P = 0.003). Twenty-four hours after SBO, histology score was 3.8 ± 1.7, which was higher than 0.9 ± 0.7 in controls (P = 0.001). Intestinal motility was decreased 24 h after SBO compared to sham controls (146.0 ± 21.4 AUC versus 198.9 ± 21.2 AUC, P = 0.003).
Conclusions:
SBO entails a time dependent epithelial damage to the mucosa. In parallel, molecular changes in the gut mucosal barrier occur as early as 3 h after the onset of SBO with a subsequent increase in permeability. Initial intestinal hypermotility is followed by a decrease in motility.
Insights
Small bowel obstruction (SBO) causes early intestinal wall damage and increased permeability. This leads to initial hypermotility, followed by decreased motility, potentially impacting organ function.
Area of Science:
- Gastroenterology
- Surgical Pathology
- Physiology
Background:
- Small bowel obstruction (SBO) is a common surgical emergency.
- Unresolved SBO can lead to multiorgan failure.
- Investigating SBO's impact on intestinal wall integrity and motility is crucial.
Purpose of the Study:
- To determine if morphological damage during SBO leads to molecular translocation.
- To assess how SBO-induced changes affect intestinal motility.
Main Methods:
- SBO was induced in mice by ligating the small intestine.
- Histological analysis evaluated intestinal wall damage.
- Intestinal motility and gut barrier permeability were measured at 3, 9, and 24 hours post-SBO.
Main Results:
- Increased intestinal permeability observed as early as 3 hours post-SBO.
- Morphological damage and increased permeability were confirmed at 9 and 24 hours.
- Intestinal motility initially increased then decreased significantly by 24 hours.
Conclusions:
- SBO causes time-dependent epithelial damage and increased mucosal permeability.
- Molecular changes in the gut barrier occur early in SBO.
- SBO results in a biphasic change in intestinal motility: initial hypermotility followed by hypomotility.
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