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Intercellular adhesion molecule-1 expression in dextran sodium sulfate-induced colitis in rats
M A Breider1, M Eppinger, A Gough
1Department of Pathology and Experimental Toxicology, Parke-Davis Pharmaceutical Research Division of Warner-Lambert Co., Ann Arbor, MI, USA. breidem@aa.wl.com
Veterinary Pathology
|December 13, 1997
Summary
Dextran sodium sulfate (DSS) causes colitis in rats, leading to gut inflammation and damage. This study shows that increased intercellular adhesion molecule-1 (ICAM-1) expression in the colon is an early indicator of this inflammation.
Area of Science:
- Gastroenterology
- Immunology
- Pathology
Background:
- Dextran sodium sulfate (DSS) is used to induce colitis in rodent models.
- The exact mechanisms behind DSS-induced colitis, including epithelial damage and inflammation, are not fully understood.
Purpose of the Study:
- To investigate the temporal relationship between colonic mucosal inflammation and crypt epithelial damage in DSS-induced colitis.
- To assess the expression of intercellular adhesion molecule-1 (ICAM-1) as an early marker of inflammation.
Main Methods:
- Adult male Wistar rats were administered 5.0% DSS in drinking water for 2-6 days.
- Clinical signs, gross pathology, and histological changes were evaluated.
- Immunohistochemistry and Northern blot analysis were used to assess ICAM-1 expression in the colonic mucosa.
Main Results:
- Clinical signs included rectal hemorrhage by days 5-6, correlating with colonic hemorrhage.
- Histological analysis revealed mucosal erosion, goblet cell loss, crypt dilation, and inflammatory infiltrates, progressing over time.
- Enhanced ICAM-1 expression was detected in the colonic mucosa as early as day 2, with sustained increases through day 6.
Conclusions:
- Enhanced expression of ICAM-1 in colonic mucosal endothelial cells is an early event in the inflammatory process of DSS-induced colitis.
- ICAM-1 expression precedes or coincides with significant epithelial damage, suggesting its role in the early inflammatory cascade.