Oxyresveratrol Ameliorates Dextran Sulfate Sodium-Induced Colitis in Rats by Suppressing Inflammation

Molecules. 2021 Apr 30;26(9):2630. doi: 10.3390/molecules26092630.

Abstract

Colitis causes destruction of the intestinal mucus layer and increases intestinal inflammation. The use of antioxidants and anti-inflammatory agents derived from natural sources has been recently highlighted as a new approach for the treatment of colitis. Oxyresveratrol (OXY) is an antioxidant known to have various beneficial effects on human health, such as anti-inflammatory, antibacterial activity, and antiviral activity. The aim of this study was to investigate the therapeutic effect of OXY in rats with dextran sulfate sodium (DSS)-induced acute colitis. OXY ameliorated DSS-induced colitis and repaired damaged intestinal mucosa. OXY downregulated the expression of pro-inflammatory cytokine genes (TNF-α, IL-6, and IL-1β) and chemokine gene MCP-1, while promoting the production of anti-inflammatory cytokine IL-10. OXY treatment also suppressed inflammation via inhibiting cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression in the colon, as well as the activity of myeloperoxidase (MPO). OXY exhibited anti-apoptotic effects, shifting the Bax/Bcl-2 balance. In conclusion, OXY might improve DSS-induced colitis by restoring the intestinal mucus layer and reducing inflammation within the intestine.

Keywords: anti-inflammatory; colitis; intestinal mucus layer; oxyresveratrol.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Biomarkers
  • Colitis / drug therapy
  • Colitis / etiology
  • Colitis / metabolism
  • Colon / drug effects
  • Colon / metabolism
  • Colon / pathology
  • Cytokines / metabolism
  • Dextran Sulfate / adverse effects*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Gene Expression
  • Humans
  • Inflammation Mediators / metabolism
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Nitric Oxide Synthase Type II / metabolism
  • Organ Size / drug effects
  • Plant Extracts / pharmacology*
  • Rats
  • Spleen / drug effects
  • Spleen / metabolism
  • Spleen / pathology
  • Stilbenes / pharmacology*

Substances

  • Anti-Inflammatory Agents
  • Biomarkers
  • Cytokines
  • Inflammation Mediators
  • Plant Extracts
  • Stilbenes
  • puag-haad
  • Dextran Sulfate
  • Nitric Oxide Synthase Type II