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营养基因组学应用于炎症性肠病动物模型:富含二十碳五烯酸和花生四烯酸饮食效果的转录组分析

Nutrigenomics applied to an animal model of Inflammatory Bowel Diseases: transcriptomic analysis of the effects of eicosapentaenoic acid- and arachidonic acid-enriched diets.

作者信息

Roy Nicole, Barnett Matthew, Knoch Bianca, Dommels Yvonne, McNabb Warren

机构信息

Food, Metabolism & Microbiology Section, Food & Health Group, AgResearch Grasslands, Palmerston North, New Zealand.

出版信息

Mutat Res. 2007 Sep 1;622(1-2):103-16. doi: 10.1016/j.mrfmmm.2007.04.003. Epub 2007 Apr 19.

Abstract

In vivo models of Inflammatory Bowel Diseases (IBD) elucidate important mechanisms of chronic inflammation. Complex intestinal responses to food components create a unique "fingerprint" discriminating health from disease. Five-week-old IL10(-/-) and C57BL/6J (C57; control) mice were inoculated orally with complex intestinal microflora (CIF) and/or pure cultures of Enterococcus faecalis and E. faecalis (EF) aiming for more consistent inflammation of the intestinal mucosa. Inoculation treatments were compared to non-inoculated IL10(-/-) and C57 mice, either kept in specific pathogen free (SPF) or conventional conditions (2x5 factorial design). At 12 weeks of age, mice were sacrificed for intestinal histological (HIS) and transcriptomic analysis using limma and Ingenuity Pathway Analysis Software. Colonic HIS was significantly affected (P<0.05) in inoculated IL10(-/-) mice and accounted for approximately 60% of total intestinal HIS. Inoculation showed a strong effect on colonic gene expression, with more than 2000 genes differentially expressed in EF.CIF-inoculated IL10(-/-) mice. Immune response gene expression was altered (P<0.05) in these mice. The second study investigated the effect of arachidonic (AA) and eicosapentaenoic acid (EPA) on colonic HIS and gene expression to test whether EPA, contrary to AA, diminished intestinal inflammation in EF.CIF IL10(-/-) mice (2 x 4 factorial design). AIN-76A (5% corn oil) and AIN-76A (fat-free) +1% corn oil supplemented with either 3.7% oleic acid (OA), AA or EPA were used. IL10(-/-) mice fed EPA- and AA-enriched diets had at least 40% lower colonic HIS (P<0.05) than those fed control diets (AIN-76A and OA diets). The expression of immune response and 'inflammatory disease' genes (down-regulated: TNFalpha, IL6, S100A8, FGF7, PTGS2; up-regulated: PPARalpha, MGLL, MYLK, PPSS23, ABCB4 with EPA and/or AA) was affected in IL10(-/-) mice fed EPA- and AA-enriched diets, compared to those fed AIN-76A diet.

摘要

炎症性肠病(IBD)的体内模型阐明了慢性炎症的重要机制。肠道对食物成分的复杂反应产生了一种独特的“指纹”,可区分健康与疾病。将5周龄的IL10基因敲除小鼠和C57BL/6J(C57;对照)小鼠经口接种复杂肠道菌群(CIF)和/或粪肠球菌纯培养物,以更一致地诱发肠道黏膜炎症。将接种处理与未接种的IL10基因敲除小鼠和C57小鼠进行比较,这些小鼠分别饲养在无特定病原体(SPF)或常规条件下(2×5析因设计)。在12周龄时,处死小鼠进行肠道组织学(HIS)和转录组分析,使用limma和Ingenuity Pathway Analysis软件。接种的IL10基因敲除小鼠的结肠HIS受到显著影响(P<0.05),约占肠道总HIS的60%。接种对结肠基因表达有强烈影响,在接种EF.CIF的IL10基因敲除小鼠中有超过2000个基因差异表达。这些小鼠的免疫反应基因表达发生了改变(P<0.05)。第二项研究调查了花生四烯酸(AA)和二十碳五烯酸(EPA)对结肠HIS和基因表达的影响,以测试EPA是否与AA相反,可减轻EF.CIF IL10基因敲除小鼠的肠道炎症(2×4析因设计)。使用了AIN-76A(5%玉米油)和AIN-76A(无脂肪)+1%玉米油,并分别添加3.7%油酸(OA)、AA或EPA。与喂食对照饮食(AIN-76A和OA饮食)的小鼠相比,喂食富含EPA和AA饮食的IL10基因敲除小鼠的结肠HIS至少降低了40%(P<0.05)。与喂食AIN-76A饮食的小鼠相比,喂食富含EPA和AA饮食的IL10基因敲除小鼠的免疫反应和“炎症性疾病”基因的表达(下调:TNFα、IL6、S100A8、FGF7、PTGS2;上调:PPARα、MGLL、MYLK、PPSS23、ABCB4与EPA和/或AA)受到影响。

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