A5 DEVELOPMENT OF A PRE-CLINICAL MOUSE MODEL TO INVESTIGATE ADVERSE FOOD REACTIONS IN INTESTINAL INFLAMMATION

B. Barbosa da Luz, L. Rondeau, R. Dang, A. Caminero
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Abstract

Abstract Background Patients with chronic intestinal conditions, including inflammatory bowel disease (IBD), experience diverse food-related adverse reactions. However,, the precise mechanisms of food intolerances in IBD remains unclear. Emerging evidence suggests that altered diet-microbiota interactions can contribute to the development of IBD. Previously we shown that intestinal microbiota plays an important role in the development of food intolerances. We hypothesize that microbial alterations in IBD patients facilitate adverse reactions to foods. Aims To establish a preclinical mouse model to study adverse food reactions in intestinal inflammation. Methods Eight-week-old C57BL/6 mice were treated with 3% dextran sodium sulfate (DSS) for 5 days, then divided into three groups. The first group was sensitized to dairy protein (3% casein and 3% whey), using 4 oral administrations of cholera toxin over 2 weeks, without any further diet intervention. The second group was also sensitized to casein and whey, then after 1 week of recovery, the mice were subsequently place on a chow containing casein and whey. Finally, the third group was subjected to diet intervention without sensitization. The same experiment was repeated in a different subset of C57BL/6 mice which included a second cycle of DSS (1.5%) during the dietary interventions. Markers of intestinal inflammation (disease activity index (DAI), histological damage, cell infiltration and pro-inflammatory genes expression (NanoString)) and intestinal microbiota were analysed after 1 week of the diet intervention. Results Mice previously sensitized on the dairy diet exhibited an enhanced activation of immune cells after intestinal inflammation. While the histological damage score did not reveal significant differences among experimental groups, the sensitized group under dairy intervention exhibited an elevated level of immune cell infiltration, increasing the polymorphonuclear, CD3+ and mast cells. Gene expression also revealed that dairy induced the expression of inflammatory genes, such as C6, Arg1, Tnf, Il6, Cxcl9 and Cxcl10. When animals are subjected to a second DSS-cycle, dairy worsen colitis in mice previously sensitized, as shown by higher DAI compared to group with control diet and dairy diet without sensitization. Conclusions In the context of intestinal inflammation, dairy protein leads to immune activation characterized by an increase in polymorphonuclear cells, mast cells and lymphocytes, as well as worsening colitis. Future studies using this model will provide valuable insights into the role of intestinal microbiota in food intolerances associated with intestinal inflammation. Funding Agencies CCC
A5 建立临床前小鼠模型,研究肠道炎症中的食物不良反应
摘要 背景 炎症性肠病(IBD)等慢性肠道疾病患者会出现多种与食物有关的不良反应。然而,IBD 患者食物不耐受的确切机制仍不清楚。新的证据表明,饮食与微生物群相互作用的改变可能会导致 IBD 的发生。此前,我们曾发现肠道微生物群在食物不耐受的发病过程中发挥着重要作用。我们推测,IBD 患者体内微生物的改变会促进对食物的不良反应。目的 建立临床前小鼠模型,研究肠道炎症的食物不良反应。方法 用 3% 右旋糖酐硫酸钠(DSS)治疗八周大的 C57BL/6 小鼠 5 天,然后将其分为三组。第一组对乳制品蛋白质(3%酪蛋白和3%乳清)过敏,在2周内口服4次霍乱毒素,不再进行任何饮食干预。第二组小鼠也对酪蛋白和乳清过敏,恢复 1 周后,让它们食用含有酪蛋白和乳清的饲料。最后,第三组接受饮食干预,但不进行致敏处理。同样的实验在不同的 C57BL/6 小鼠亚群中重复进行,其中包括在饮食干预期间使用第二个周期的 DSS(1.5%)。饮食干预 1 周后,对肠道炎症指标(疾病活动指数 (DAI)、组织学损伤、细胞浸润和促炎症基因表达 (NanoString))和肠道微生物群进行分析。结果 先前对乳制品饮食过敏的小鼠在肠道炎症后表现出免疫细胞活化增强。虽然组织学损伤评分在各实验组之间没有显示出显著差异,但接受乳制品干预的致敏组显示出免疫细胞浸润水平升高,多形核细胞、CD3+细胞和肥大细胞增多。基因表达也显示,乳制品诱导了炎症基因的表达,如 C6、Arg1、Tnf、Il6、Cxcl9 和 Cxcl10。在对动物进行第二次DSS循环时,乳制品会加重先前致敏小鼠的结肠炎,这表现在与对照饮食组和未致敏乳制品饮食组相比,DAI更高。结论 在肠道炎症的背景下,乳制品蛋白质会导致以多形核细胞、肥大细胞和淋巴细胞增加以及结肠炎恶化为特征的免疫激活。今后利用该模型进行的研究将为了解肠道微生物群在与肠道炎症相关的食物不耐受中的作用提供宝贵的见解。资助机构 CCC
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