Citrus nobiletin ameliorates experimental colitis by reducing inflammation and restoring impaired intestinal barrier function

Mol Nutr Food Res. 2015 May;59(5):829-42. doi: 10.1002/mnfr.201400614. Epub 2015 Mar 16.

Abstract

Scope: Inflammatory bowel disease is a chronic inflammatory disorder of the gastrointestinal tract. Citrus nobiletin can exert robust anti-inflammatory effects in vivo and in vitro. We evaluated the impact of nobiletin on the excessive inflammatory response and impaired barrier function in a rodent colitis model.

Methods and results: Colitis was established by infusion with 1 mL 2,4,6-trinitrobenzene sulfonic acid (TNBS) dissolved in ethanol (40% v/v) in rats at a 125 mg/kg dose. Caco-2 cell monolayer exposed to LPSs is used as a culture model for intestinal permeability measurements. Nobiletin decreased rat epithelial proinflammatory cytokines and mediators production. Nobiletin restored impaired barrier function in colitic rats and Caco-2 monolayer. Nobiletin decreased protein expressions of Akt, nuclear factor-kappa B (NF-κB), and myosin light chain kinase (MLCK) isolated from rat intestinal epithelial tissue and Caco-2 cell, respectively. PI3K inhibitor or siRNA targeting of either Akt or NF-κB mitigated the impact of nobiletin on MLCK expression and barrier function in Caco-2 monolayer, respectively.

Conclusion: Nobiletin exerted anti-inflammatory effects in TNBS-induced colitis through the downregulation of inducible nitric oxide synthase (iNOS) and cyclooxygenase 2 (COX-2) expression. Nobiletin restored barrier function, which had been damaged after TNBS administration, through the inhibition of the Akt-NF-κB-MLCK pathway.

Keywords: Akt; Colitis; Impaired barrier function; NF-κB; Nobiletin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Caco-2 Cells
  • Citrus / chemistry*
  • Colitis / drug therapy*
  • Colitis / immunology
  • Colitis / metabolism
  • Cytokines / analysis
  • Flavones / pharmacology*
  • Humans
  • Intestinal Mucosa / metabolism
  • Intestines / drug effects*
  • Male
  • Myosin-Light-Chain Kinase / antagonists & inhibitors
  • NF-kappa B / antagonists & inhibitors
  • Neutrophil Infiltration / drug effects
  • Permeability
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Trinitrobenzenesulfonic Acid

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Flavones
  • NF-kappa B
  • Trinitrobenzenesulfonic Acid
  • nobiletin
  • Proto-Oncogene Proteins c-akt
  • Myosin-Light-Chain Kinase