Mucosal colonisation with Lactobacillus casei mitigates barrier injury induced by exposure to trinitronbenzene sulphonic acid

Gut. 2005 Jul;54(7):955-9. doi: 10.1136/gut.2004.056101.

Abstract

Background: Trinitrobenzene sulphonic acid (TNBS) induces chronic transmural inflammatory lesions in the rat colon. Injury is facilitated by barrier disruption and invasion of commensal bacteria. However, certain bacteria have shown anti-inflammatory properties in in vitro models.

Aim: To investigate in vivo the anti-inflammatory effect of Lactobacillus casei DN-114 001.

Methods: Rats with a colonic segment excluded from faecal transit were surgically prepared. After washing the lumen with antibiotics, the excluded segment was recolonized (control group: standard flora of rat origin; test group: standard flora and L casei). Microbial colonisation was confirmed by culture of segment washing, and colitis was then induced by instillation of TNBS. One day after, intestinal lesions were blindly graded by macro- and microscopic scores, and myeloperoxidase activity measured in tissue homogenates. Translocation of bacteria to mesenteric lymph nodes, spleen and liver was investigated.

Results: Test rats showed a smaller area of mucosal injury than control rats (p<0.05). Maximum depth lesion scores were similar in both groups but myeloperoxidase activity was lower in test than in control rats (p<0.05). Remarkably, bacterial translocation was quantitatively lower (p<0.01) and less frequent (p<0.05) in test than in control rats.

Conclusion: In rats colonised with L casei, mucosal injury, inflammatory response, and barrier disruption after TNBS challenge were attenuated. Bacterial communities colonising the mucosa can modify inflammatory responses to luminal challenges.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Translocation
  • Colitis, Ulcerative / chemically induced
  • Colitis, Ulcerative / microbiology
  • Colitis, Ulcerative / therapy*
  • Colon / microbiology
  • Disease Models, Animal
  • Intestinal Absorption
  • Intestinal Mucosa / microbiology*
  • Lacticaseibacillus casei / physiology*
  • Liver / microbiology
  • Lymph Nodes / microbiology
  • Male
  • Peroxidase / metabolism
  • Probiotics / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Spleen / microbiology
  • Trinitrobenzenesulfonic Acid

Substances

  • Trinitrobenzenesulfonic Acid
  • Peroxidase