4.5 Article

A New Rat Model of Pouchitis After Proctocolectomy and Ileal Pouch-Anal Anastomosis Using 2,4,6-Trinitrobenzene Sulfonic Acid

Journal

JOURNAL OF GASTROINTESTINAL SURGERY
Volume 25, Issue 6, Pages 1524-1533

Publisher

SPRINGER
DOI: 10.1007/s11605-020-04642-2

Keywords

Pouchitis; 2; 4; 6-Trinitrobenzene sulfonic acid; Dextran sulfate sodium; Proctocolectomy and ileal pouch-anal anastomosis; Ulcerative colitis

Funding

  1. Li Jie-shou Gut Barrier Foundation [LJS_201008]

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We established an animal model resembling human pouchitis by evaluating general status, fecal microbiota diversity, and expression of inflammatory markers. We found that the TNBS-induced model showed more stable weight changes and dysbacteriosis compared to the DSS-induced model. This model could effectively mimic the characteristics of human pouchitis and be used for further research.
Background Pouchitis is a common complication after ileal pouch-anal anastomosis (IPAA) in patients with ulcerative colitis. However, an ideal model remains lacking. Therefore, we aimed to establish an appropriate model resembling human pouchitis. Methods Sprague-Dawley rats were randomly assigned to five groups: TNBS group, DSS group, NS group (following IPAA procedure, administrated with TNBS enema, DSS orally, normal saline enema, respectively), NI group (underwent IPAA), and sham group (underwent switch abdominal surgery). General status, weight change, hematochezia, and fecal scores were recorded. Fecal microbiota were counted under a microscope and analyzed by 16S rRNA gene high-throughput sequencing. Specimens of ileal pouch and small intestine (proximal, mid, distal) were collected to evaluate myeloperoxidase and occludin expression by immunohistochemistry and mRNA expression of pro-inflammatory markers by PCR. Results General status, hematochezia, fecal score, and increased mRNA expression of interleukin-6 and TNF-alpha in the TNBS group were similar to those in the DSS group, whereas the TNBS-induced model displayed a more stable weight change and more serious dysbacteriosis, not only was fecal bacterial diversity reduced, the dominant microbiota was altered. Histopathology scores of the distal small intestine in the TNBS group were lower compared with those in the DSS group (P < 0.05). A significant difference in myeloperoxidase and occludin expression in the small intestine was also detected between the TNBS and DSS groups. Conclusions Our model mimicked the characteristics of human pouchitis and avoided potential side effects in the small intestine, and thus could be employed for further research.

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