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Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles.

Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles. Research Abstract Details 

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  • Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles. Abstract Text:

    harris bernsteinHarris Bernstein,hana holubecHana Holubec,carol bernsteinCarol Bernstein,natalia a ignatenkoNatalia A Ignatenko,eugene gernerEugene Gerner,katerina dvorakKaterina Dvorak,david besselsenDavid Besselsen,karen ann blohm-mangoneKaren Ann Blohm-Mangone,jose padilla-torresJose Padilla-Torres,barbora dvorakovaBarbora Dvorakova,harinder garewalHarinder Garewal,claire m payneClaire M Payne,

    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.

    Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles. Publishing Authors By Initials

    h bernsteinH Bernstein,h holubecH Holubec,c bernsteinC Bernstein,na ignatenkoNA Ignatenko,e gernerE Gerner,k dvorakK Dvorak,d besselsenD Besselsen,ka blohm-mangoneKA Blohm-Mangone,j padilla-torresJ Padilla-Torres,b dvorakovaB Dvorakova,h garewalH Garewal,cm payneCM Payne,

    For similar cells: cellular structures: cell membrane: cell membrane structures: intercellular junctions: tight junctions research abstracts see: cells: cellular structures: cell membrane: cell membrane structures: intercellular junctions: tight junctions research

    PUBMED ID PMID:

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    Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Digestive diseases and sciences

    VOLUME: 52

    Page Numbers: 628-42

    Journal Abbreviation:

    ISSN: 0163-2116

    DAY: 3

    MONTH: Mar

    YEAR: 2007

    Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7902782

    Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles. Keywords Mesh Terms:

    KEYWORDS: Tight Junctions

    MESH TERMS: physiology

    Chemical & Substance for Abstract: Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles. Information

    Substance Name: Nitric Oxide Synthase

    Registry Number: EC 1.14.13.39

    Grant and Affiliation Information for Deoxycholate-induced colitis is markedly attenuated in Nos2 knockout mice in association with modulation of gene expression profiles.

    AFFILIATION: Department of Cell Biology and Anatomy, College of Medicine, University of Arizona, Tucson, Arizona 85724-5044, USA. bernstein3@earthlink.net

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: CA72008

    ACRONYM: CA

    MEDLINETA: Dig Dis Sci

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