International Journal of Colorectal Disease

, Volume 16, Issue 4, pp 238–246

Clinical and histopathological features of dextran sulfate sodium induced acute and chronic colitis associated with dysplasia in rats

Authors

  • Frank Kullmann
    • Department of Internal Medicine I, University of Regensburg, 93042 Regensburg, Germany
  • Helmut Messmann
    • Department of Internal Medicine I, University of Regensburg, 93042 Regensburg, Germany
  • Marianne Alt
    • Department of Internal Medicine I, University of Regensburg, 93042 Regensburg, Germany
  • Volker Gross
    • Department of Internal Medicine I, University of Regensburg, 93042 Regensburg, Germany
  • Tina Bocker
    • Institute of Pathology, Jefferson University, Philadelphia, Pa., USA
  • Jürgen Schölmerich
    • Department of Internal Medicine I, University of Regensburg, 93042 Regensburg, Germany
  • Josef Rüschoff
    • Institute of Pathology, Klinikum Kassel, Moenckebergstrasse 41-44, 34125 Kassel, Germany
Original Article

DOI: 10.1007/s003840100311

Cite this article as:
Kullmann, F., Messmann, H., Alt, M. et al. Int J Colorectal Dis (2001) 16: 238. doi:10.1007/s003840100311

Abstract.

We examined the clinical and histopathological features of the dextran sulfate sodium (DSS) induced acute and chronic colitis in rats as a model for studying basic biology of the inflamed colonic mucosa. Acute colitis was induced in male Wistar rats by 4 days (AI) or 7 days (AII) of oral 5% (wt/vol) DSS (mol. wt. 54,000) in their drinking water. Chronic colitis was induced in 8 experimental groups: CI=7 days DSS followed by 10 days water (=one cycle); CII=two cycles; CIII to CVIII (three to eight cycles) received only 4 days 5% DSS followed by 10 days drinking water. The entire colons were examined histologically; dysplasia was graded as: indefinite/probably negative for dysplasia, indefinite/probably positive for dysplasia, low-grade dysplasia, or high-grade dysplasia. The earliest clinical findings in the acute colitis group over 4 days occurred on day 2 (hemoccult positive stools, loose stools or diarrhea and weight loss). The maximal disease activity was noted on day 7 accompanied by a 53% mortality rate. The histological inflammation scores were significantly higher on day 7 than on day 4. All rats had extensive ulcerations predominantly in the rectum and cecum. The number of rats having ulcerations was markedly lower in the chronic colitis groups. The majority (75%) of the crypt lesions suspicious for dysplasia were classified as mucosa indefinite/probably negative for dysplasia. We classified 18 crypt lesions as low-grade dysplasia and one lesion as high-grade dysplasia (after eight cycles). No invasive carcinoma was observed. Most low-grade dysplasias (83%) occurred after five cycles of DSS/water, located mostly in the rectum (44%) and colon transversum (33%). Our findings suggest that the DSS colitis model in rats may be an interesting model for studying the sequence chronic inflammation-dysplasia in human ulcerative colitis. Further long-term studies with the present DSS colitis model in rats might also prove it as a reliable model to study the sequence high-grade dysplasia and colitis associated-cancer.

Dextran sulfate sodium Dysplasia Inflammation Rats Ulcerative colitis

Copyright information

© Springer-Verlag 2001