ICC density predicts bacterial overgrowth in a rat model of post-infectious IBS

World J Gastroenterol. 2010 Aug 7;16(29):3680-6. doi: 10.3748/wjg.v16.i29.3680.

Abstract

Aim: To investigate the interstitial cells of Cajal (ICC) number using a new rat model.

Methods: Sprague-Dawley rats were assigned to two groups. The first group received gavage with Campylobacter jejuni (C. jejuni) 81-176. The second group was gavaged with placebo. Three months after clearance of Campylobacter from the stool, precise segments of duodenum, jejunum, and ileum were ligated in self-contained loops of bowel that were preserved in anaerobic bags. Deep muscular plexus ICC (DMP-ICC) were quantified by two blinded readers assessing the tissue in a random, coded order. The number of ICC per villus was compared among controls, Campylobacter recovered rats without small intestinal bacterial overgrowth (SIBO), and Campylobacter recovered rats with SIBO.

Results: Three months after recovery, 27% of rats gavaged with C. jejuni had SIBO. The rats with SIBO had a lower number of DMP-ICC than controls in the jejunum and ileum. Additionally there appeared to be a density threshold of 0.12 DMP-ICC/villus that was associated with SIBO. If ileal density of DMP-ICC was < 0.12 ICC/villus, 54% of rats had SIBO compared to 9% among ileal sections with > 0.12 (P < 0.05). If the density of ICC was < 0.12 DMP-ICC/villus in more than one location of the bowel, 88% of these had SIBO compared to 6% in those who did not (P < 0.001).

Conclusion: In this post-infectious rat model, the development of SIBO appears to be associated with a reduction in DMP-ICC. Further study of this rat model might help understand the pathophysiology of post-infectious irritable bowel syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Campylobacter Infections / complications*
  • Campylobacter jejuni / metabolism*
  • Campylobacter jejuni / pathogenicity
  • Cell Count*
  • Feces / microbiology
  • Interstitial Cells of Cajal / cytology*
  • Intestine, Small* / anatomy & histology
  • Intestine, Small* / microbiology
  • Intestine, Small* / physiopathology
  • Irritable Bowel Syndrome* / etiology
  • Irritable Bowel Syndrome* / microbiology
  • Irritable Bowel Syndrome* / physiopathology
  • Rats
  • Rats, Sprague-Dawley