Sclareol protected against intestinal barrier dysfunction ameliorating Crohn's disease-like colitis via Nrf2/NF-B/MLCK signalling

Int Immunopharmacol. 2024 May 30:133:112140. doi: 10.1016/j.intimp.2024.112140. Epub 2024 Apr 25.

Abstract

Background: Inflammation-induced intestinal barrier dysfunction is not only a pathological feature of Crohn's disease (CD) but also an important therapeutic target. Sclareol (SCL) is a nontoxic natural plant compound with anti-inflammatory effect, but its role in CD has not been established.

Methods: In vivo studies of mice with TNBS-induced colitis were carried out to evaluate the effects of SCL on CD-like colitis and intestinal barrier function. In vitro, a TNF-α-induced colonic organoid model was established to test the direct effect of SCL on inflammation-induced intestinal barrier injure and inflammatory response. The Nrf2/NF-κB/MLCK signalling was analysed to explore the mechanism of SCL.

Results: In vivo, SCL largely alleviated the colitis in TNBS mice, as evidenced by improvements in the weight loss, colitis symptoms, endoscopic score, macroscopic histological score, and histological inflammation score. Moreover, SCL significantly improved intestinal barrier dysfunction, manifested as reduced intestinal permeability and decreased intestinal bacterial translocation in TNBS mice. Importantly, SCL antagonised the intestinal mucosal inflammation while protecting tight junctions in TNBS mice. In vitro, SCL largely depressed pro-inflammatory cytokines levels and improved intestinal epithelial permeability in a TNF-α-induced colonic organoid model. In the context of CD, the protective effects of SCL against inflammation and intestinal barrier damage are at least partially results from the Nrf2 signalling activation and the NF-κB/MLCK signalling inhibition.

Conclusions: SCL improved intestinal barrier dysfunction and alleviated CD-like colitis, possibly through modulation of Nrf2/NF-κB/MLCK signalling. In view of SCL's safety profile, there is hope that it will be useful in the clinic.

Keywords: Colonic organoids; Crohn's disease; Intestinal barrier function; Phytopharmaceutical; Sclareol.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / therapeutic use
  • Colitis* / chemically induced
  • Colitis* / drug therapy
  • Colitis* / pathology
  • Colon / drug effects
  • Colon / pathology
  • Crohn Disease* / drug therapy
  • Crohn Disease* / pathology
  • Disease Models, Animal
  • Diterpenes / pharmacology
  • Diterpenes / therapeutic use
  • Humans
  • Intestinal Mucosa* / drug effects
  • Intestinal Mucosa* / metabolism
  • Intestinal Mucosa* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myosin-Light-Chain Kinase / metabolism
  • NF-E2-Related Factor 2* / metabolism
  • NF-kappa B* / metabolism
  • Permeability / drug effects
  • Signal Transduction* / drug effects
  • Trinitrobenzenesulfonic Acid*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • NF-E2-Related Factor 2
  • NF-kappa B
  • Nfe2l2 protein, mouse
  • Trinitrobenzenesulfonic Acid
  • Anti-Inflammatory Agents
  • Myosin-Light-Chain Kinase
  • Diterpenes
  • Tumor Necrosis Factor-alpha