Direct evidence of oxidative damage in acute and chronic phases of experimental colitis in rats

Dig Dis Sci. 1996 Jun;41(6):1204-11. doi: 10.1007/BF02088238.


During inflammatory colitis in man and experimental animals, the production of free radicals increases. This study evaluated the histological pattern and biochemical parameters of oxidative damage during acute and chronic colitis induced by 2,4,-trinitrobenzenesulfonic acid + ethanol in rats. On the samples of scraped mucosa of six groups of rats, one not treated, one killed after 1 hr, and those killed one, two, four, and eight weeks after the induced-damage, we determined the histological and superoxide dismutase activity and the concentration of lipoperoxides, malonyldialdheyde, and reduced glutathione. After 1 hr, the mucosal damage and superoxide dismutase activity were slight; glutathione, lipoperoxides, and malonyldialdheyde were significantly increased. At one week, the histological damage was severe, decreasing progressively, and significantly correlated to superoxide dismutase activity. Lipoperoxides and malonyldialdheyde were high throughout the study. Glutathione was significantly increased at one and two weeks and dramatically decreased thereafter. Therefore, in experimental colitis the cascade of free-radical production induces a constant self-maintaining lipoperoxidation and consumes the cellular antioxidant capability.

MeSH terms

  • Acute Disease
  • Animals
  • Chronic Disease
  • Colitis / chemically induced
  • Colitis / metabolism*
  • Colitis / pathology
  • Colon / metabolism*
  • Colon / pathology
  • Ethanol
  • Glutathione / metabolism
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Lipid Peroxidation
  • Male
  • Malondialdehyde / metabolism
  • Oxidative Stress*
  • Rats
  • Rats, Wistar
  • Superoxide Dismutase / metabolism
  • Trinitrobenzenesulfonic Acid


  • Ethanol
  • Malondialdehyde
  • Trinitrobenzenesulfonic Acid
  • Superoxide Dismutase
  • Glutathione