TY - JOUR
T1 - Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles
AU - Bernstein, Harris
AU - Holubec, Hana
AU - Bernstein, Carol
AU - Ignatenko, Natalia
AU - Gerner, Eugene
AU - Dvorak, Katerina
AU - Besselsen, David
AU - Blohm-Mangone, Karen Ann
AU - Padilla-Torres, Jose
AU - Dvorakova, Barbora
AU - Garewal, Harinder
AU - Payne, Claire M.
N1 - Funding Information:
Acknowledgments This work was supported in part by NIH Institutional Core Grant CA23074, NIH-PPG CA72008, Arizona Disease Control Research Commission Grants 10016 and 6002, VAH Merit Review Grant 2HG, NCI SPORE Grant 1P50CA95060–01, NIH 1R21CA111513–01A1, and Biomedical Diagnostics & Research, Inc., Tucson, Arizona.
PY - 2007/3
Y1 - 2007/3
N2 - 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.
AB - 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.
KW - Colitis
KW - Colon cancer
KW - Deoxycholate
KW - Inflammatory bowel disease
KW - Nitric oxide synthase
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U2 - 10.1007/s10620-006-9608-0
DO - 10.1007/s10620-006-9608-0
M3 - Article
C2 - 17253130
AN - SCOPUS:33847218653
SN - 0163-2116
VL - 52
SP - 628
EP - 642
JO - Digestive diseases and sciences
JF - Digestive diseases and sciences
IS - 3
ER -