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Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles
- Source :
- Digestive diseases and sciences. 52(3)
- Publication Year :
- 2006
-
Abstract
- Nos2 knockout mice were compared to wild-type mice for susceptibility to colitis in response to a diet supplemented with deoxycholate, a bile acid increased in the colon of individuals on a high-fat diet. Wild-type mice fed a fat-related diet, supplemented with 0.2% DOC, develop colonic inflammation associated with increases in nitrosative stress, proliferation, oxidative DNA/RNA damage, and angiogenesis, as well as altered expression of numerous genes. However, Nos2 knockout mice fed a diet supplemented with deoxycholate were resistant to these alterations. In particular, 35 genes were identified whose expression was significantly altered at the mRNA level in deoxycholate-fed Nos2(+/+) mice but not in deoxycholate-fed Nos2(–/–) mice. Some of these alterations in NOS2-dependent gene expression correspond to those reported in human inflammatory bowel disease. Overall, our results indicate that NOS2 expression is necessary for the development of deoxycholate-induced colitis in mice, a unique dietary-related model of colitis.
- Subjects :
- medicine.medical_specialty
Physiology
medicine.drug_class
Ratón
Detergents
Inflammation
Mice, Inbred Strains
Inflammatory bowel disease
Tight Junctions
Mice
Internal medicine
parasitic diseases
Gene expression
medicine
Animals
Colitis
Intestinal Mucosa
Oligonucleotide Array Sequence Analysis
Bile acid
business.industry
Gene Expression Profiling
Gastroenterology
Membrane Proteins
respiratory system
medicine.disease
Ulcerative colitis
Immunohistochemistry
Disease Models, Animal
Oxidative Stress
Endocrinology
Immunology
Knockout mouse
Dietary Supplements
Disease Progression
medicine.symptom
Nitric Oxide Synthase
business
DNA Damage
Deoxycholic Acid
Subjects
Details
- ISSN :
- 01632116
- Volume :
- 52
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Digestive diseases and sciences
- Accession number :
- edsair.doi.dedup.....a068bbe34f3dbc5479d969b1853947fb