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脱氧胆酸盐诱导的结肠炎在Nos2基因敲除小鼠中明显减轻,且与基因表达谱的调节有关。

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

作者信息

Bernstein Harris, Holubec Hana, Bernstein Carol, Ignatenko Natalia A, Gerner Eugene, Dvorak Katerina, Besselsen David, Blohm-Mangone Karen Ann, Padilla-Torres Jose, Dvorakova Barbora, Garewal Harinder, Payne Claire M

机构信息

Department of Cell Biology and Anatomy, College of Medicine, University of Arizona, Tucson, Arizona 85724-5044, USA.

出版信息

Dig Dis Sci. 2007 Mar;52(3):628-42. doi: 10.1007/s10620-006-9608-0.

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.

摘要

将Nos2基因敲除小鼠与野生型小鼠进行比较,以研究它们在食用添加脱氧胆酸盐(一种在高脂饮食个体结肠中含量增加的胆汁酸)的饮食后对结肠炎的易感性。喂食添加0.2%脱氧胆酸盐的脂肪相关饮食的野生型小鼠会出现结肠炎症,伴有亚硝化应激增加、细胞增殖、氧化DNA/RNA损伤和血管生成,以及众多基因表达的改变。然而,喂食添加脱氧胆酸盐饮食的Nos2基因敲除小鼠对这些改变具有抗性。特别是,鉴定出35个基因,其在喂食脱氧胆酸盐的Nos2(+/+)小鼠的mRNA水平上表达显著改变,但在喂食脱氧胆酸盐的Nos2(-/-)小鼠中未改变。这些NOS2依赖性基因表达的一些改变与人类炎症性肠病中报道的改变相对应。总体而言,我们的结果表明,NOS2表达对于小鼠中脱氧胆酸盐诱导的结肠炎的发展是必要的,这是一种独特的饮食相关结肠炎模型。

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