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Mucosal colonisation with Lactobacillus casei mitigates barrier injury induced by exposure to trinitronbenzene sulphonic acid
  1. M Llopis1,
  2. M Antolín1,
  3. F Guarner1,
  4. A Salas2,
  5. J-R Malagelada1
  1. 1Digestive System Research Unit, University Hospital Vall d’Hebron, Autonomous University of Barcelona, Barcelona, Spain
  2. 2Department of Pathology, Hospital Mutua de Terrassa, Terrassa, Spain
  1. Correspondence to:
    Dr F Guarner
    Digestive System Research Unit, Hospital General Vall d’Hebron, Barcelona 08035, Spain; fguarneramedynet.com

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 recolonised (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.

  • TNBS, trinitrobenzene sulphonic acid
  • MPO, myeloperoxidase
  • CFU, colony forming units
  • MLN, mesenteric lymph nodes
  • MRS, De Man Rogosa Sharp medium
  • probiotics
  • colitis
  • bacterial translocation
  • inflammation
  • lactobacillus
  • mucosal barrier trinitrobenzene sulphonic acid

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Footnotes

  • Conflict of interest: None declared.

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