Author/Authors :
Taghipour, Niloofar Gastroenterology and Liver Diseases Research Center - Research Institute for Gastroenterology and Liver Diseases - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Molaei, Mahsa Gastroenterology and Liver Diseases Research Center - Research Institute for Gastroenterology and Liver Diseases - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Mosaffa, Nariman Immunology Department - Faculty of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Rostami-Nejad, Mohammad Gastroenterology and Liver Diseases Research Center - Research Institute for Gastroenterology and Liver Diseases - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Asadzadeh Aghdaei, Hamid Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center - Research Institute for Gastroenterology and Liver Diseases - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Anissian, Ali Department of veterinary - College of Agriculture - Islamic Azad University, Abhar branch, Iran , Azimzadeh, Pedram Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center - Research Institute for Gastroenterology and Liver Diseases - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Zali, Mohammad Reza Gastroenterology and Liver Diseases Research Center - Research Institute for Gastroenterology and Liver Diseases - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Aim: To induce acute colitis progresses to chronicity in C57BL/6 mice by dextran sulfate sodium.
Background: Murine models are essential tools to understand IBD pathogenesis. Among different types of chemically
induced colitis models, the dextran sulfate sodium (DSS)-induced colitis model is the most common model of IBD, due
to its simplicity.
Patients and methods: Male C57BL/6 mice 6–8 weeks old, were collected and matched by age with controls. C57BL/6 mice
treated with 2 cycles of 3.5% DSS for 4 days and 4 days of pure water between each cycle. After that, mice were sacrificed and
the entire colon was removed. Small sections of the colon were fixed in formaldehyde, embedded in paraffin and sectioned
with a microtome. Sections were stained with hematoxylin eosin to analyses the degree of inflammation.
Results: After the first cycle oral administration of DSS, mice with severe and visible rectal bleeding and diarrhea
entered into the acute phase. After day 4-5, bleeding and diarrhea were improved and mice entered into the chronic
phase with peak levels of weight loss. Macroscopically, the inflammation was predominantly located in the distal colon.
Microscopically, examination of the distal colon sections showed a decrease number of goblet cells, loss of crypts, signs
of surface epithelial regeneration and moderate to severe infiltration of inflammatory cells in the mucosa.
Conclusion: In order to achieve an experimental colitis model, our protocol is recommended for future therapies in IBD
experimental modeling.
Keywords :
Inflammatory bowel disease , Murine models , DSS , C57BL/6