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
Department of Cell Biology and Anatomy, College of Medicine, University of Arizona, Tucson, Arizona 85724-5044, USA.
Dig Dis Sci. 2007 Mar;52(3):628-42. doi: 10.1007/s10620-006-9608-0.
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.
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。