Effect of rectal administration of rebamipide on dextran sulfate sodium-induced colitis: role of hepatocyte growth factor

Inflamm Res. 2007 Jun;56(6):240-5. doi: 10.1007/s00011-007-6100-z.


Objective and design: Since rebamipide is effective for the treatment of ulcerative colitis (UC), we examined the involvement of hepatocyte growth factor (HGF) in the action of rebamipide.

Materials: Fifty-five and forty female Balb/c mice, respectively, were used in Exp. 1 and 2.

Treatment: 50 mg/kg/day rebamipide (Exp. 1) and 1 x 10(7) pfu pAxCAHGF (the CAG promoter-driving HGF gene in adenovirus vector) (Exp. 2) were intrarectally introduced after induction of colitis by 4 % dextran sulfate sodium (DSS).

Methods: Therapeutic effects were assessed by cell proliferation and apoptosis.

Results: Rebamipide caused proliferation of epithelial cells at 10 days after treatment, and decreased apoptosis at 10, 14 and 21 days, compared with controls. Expression of HGF was greatly increased in rebamipide-treated mice. pAxCAHGF caused cell proliferation and apoptosis, which showed the same pattern as with rebamipide treatment.

Conclusions: Rectal administration of rebamipide is effective for DSS-induced colitis in association with induction of HGF.

MeSH terms

  • Administration, Rectal
  • Alanine / administration & dosage
  • Alanine / analogs & derivatives*
  • Animals
  • Anticoagulants / toxicity
  • Apoptosis
  • Cell Proliferation
  • Colitis / chemically induced
  • Colitis / drug therapy*
  • Colitis / metabolism
  • Dextran Sulfate / toxicity*
  • Enzyme Inhibitors / administration & dosage
  • Epithelial Cells / cytology
  • Female
  • Hepatocyte Growth Factor / metabolism*
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Mice
  • Mice, Inbred BALB C
  • Quinolones / administration & dosage*


  • Anticoagulants
  • Enzyme Inhibitors
  • Quinolones
  • Hepatocyte Growth Factor
  • Dextran Sulfate
  • rebamipide
  • Alanine