Rebamipide ameliorates radiation-induced intestinal injury in a mouse model

Toxicol Appl Pharmacol. 2017 Aug 15:329:40-47. doi: 10.1016/j.taap.2017.05.012. Epub 2017 May 16.

Abstract

Radiation-induced enteritis is a major side effect in cancer patients undergoing abdominopelvic radiotherapy. Radiation exposure produces an uncontrolled inflammatory cascade and epithelial cell loss leading to impaired epithelial barrier function. The goal of this study was to determine the effect of rebamipide on regeneration of the intestinal epithelia after radiation injury. The abdomens of C57BL/6 mice were exposed to 13Gy of irradiation (IR) and then the mice were treated with rebamipide. Upon IR, intestinal epithelia were destroyed structurally at the microscopic level and bacterial translocation was increased. The intestinal damage reached a maximum level on day 6 post-IR and intestinal regeneration occurred thereafter. We found that rebamipide significantly ameliorated radiation-induced intestinal injury. In mice treated with rebamipide after IR, intestinal barrier function recovered and expression of the tight junction components of the intestinal barrier were upregulated. Rebamipide administration reduced radiation-induced intestinal mucosal injury. The levels of proinflammatory cytokines and matrix metallopeptidase 9 (MMP9) were significantly reduced upon rebamipide administration. Intestinal cell proliferation and β-catenin expression also increased upon rebamipide administration. These data demonstrate that rebamipide reverses impairment of the intestinal barrier by increasing intestinal cell proliferation and attenuating the inflammatory response by inhibiting MMP9 and proinflammatory cytokine expression in a murine model of radiation-induced enteritis.

Keywords: Barrier function; Intestine; Radiotherapy; Rebamipide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine / analogs & derivatives*
  • Alanine / pharmacology
  • Animals
  • Bacterial Translocation / drug effects
  • Bacterial Translocation / radiation effects
  • Cell Proliferation / drug effects
  • Cytokines / metabolism
  • Cytoprotection
  • Dose-Response Relationship, Drug
  • Enteritis / metabolism
  • Enteritis / pathology
  • Enteritis / prevention & control*
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Epithelial Cells / radiation effects
  • Inflammation Mediators / metabolism
  • Intestinal Mucosa / drug effects*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Intestinal Mucosa / radiation effects
  • Male
  • Matrix Metalloproteinase 9 / metabolism
  • Mice, Inbred C57BL
  • Quinolones / pharmacology*
  • Radiation Injuries, Experimental / metabolism
  • Radiation Injuries, Experimental / pathology
  • Radiation Injuries, Experimental / prevention & control*
  • Radiation-Protective Agents / pharmacology*
  • Tight Junctions / drug effects
  • Tight Junctions / metabolism
  • Tight Junctions / pathology
  • Tight Junctions / radiation effects
  • Time Factors
  • beta Catenin / metabolism

Substances

  • CTNNB1 protein, mouse
  • Cytokines
  • Inflammation Mediators
  • Quinolones
  • Radiation-Protective Agents
  • beta Catenin
  • Matrix Metalloproteinase 9
  • Mmp9 protein, mouse
  • rebamipide
  • Alanine