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Updated: Jun 3, 2025

Murine Colitis Modeling using Dextran Sulfate Sodium DSS
Published on: January 19, 2010
CHONDROITIN SULFATE AND GLUCOSAMINE SULFATE AS PROTECTIVE AND ANTI-INFLAMMATORY AGENTS IN THE ULCERATIVE COLITIS DSS
Luiz Gustavo de Oliveira1, Arthur Girardi Carpanez1, João Victor Gerheim da Silva1
1Instituto de Ciências Biológicas da Universidade Federal de Juiz de Fora, Laboratório de Análises de Glicoconjugados, Departamento de Bioquímica, Juiz de Fora, MG, Brasil.
Chondroitin sulfate (CS) and glucosamine (GlcN) reduce intestinal inflammation and protect the gut barrier in a rat model of ulcerative colitis. This combination therapy shows promise for treating inflammatory bowel disease (IBD).
Area of Science:
- Biochemistry
- Pharmacology
- Gastroenterology
Background:
- Chondroitin sulfate (CS) and glucosamine (GlcN) are known for anti-inflammatory properties, particularly in reducing metalloproteinases (MMP) and inflammatory mediators.
- Ulcerative colitis (UC) is a chronic inflammatory bowel disease (IBD) characterized by intestinal inflammation and barrier dysfunction.
Purpose of the Study:
- To investigate the structure of CS.
- To evaluate the anti-inflammatory and protective effects of CS/GlcN in a rat model of dextran sulfate sodium (DSS)-induced ulcerative colitis.
Main Methods:
- Characterization of CS structure and molecular weight.
- Oral administration of CS/GlcN to rats with DSS-induced colitis.
- Assessment of histological scores, goblet cell destruction, nitric oxide (NO) production, myeloperoxidase (MPO) activity, and MMP activity (specifically MMP-9).
- Evaluation of cytotoxicity of CS/GlcN on intestinal epithelial cells.
Main Results:
- CS disaccharide composition was similar to the C4S standard, with a modal molecular weight of 30.4 kDa.
- Oral CS/GlcN administration significantly improved acute colitis severity, reducing histological scores and goblet cell destruction.
- A decrease in NO production, MPO activity, and MMP activity (especially MMP-9) was observed.
- CS/GlcN demonstrated no cytotoxicity in intestinal epithelial cells.
Conclusions:
- CS/GlcN combination therapy effectively reduced intestinal inflammation and protected the intestinal barrier in a rat model of colitis.
- These findings suggest that CS/GlcN may be a beneficial therapeutic option for inflammatory bowel disease (IBD).
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