Funda David P, Kaas Anne, Tlaskalová-Hogenová Helena, Buschard Karsten
Division of Immunology and Gnotobiology, Institute of Microbiology, Czech Academy of Sciences, Prague, Czech Republic.
Diabetes Metab Res Rev. 2008 Jan-Feb;24(1):59-63. doi: 10.1002/dmrr.748.
Environmental factors such as nutrition or exposure to infections play a substantial role in the pathogenesis of type 1 diabetes (T1D). We have previously shown that gluten-free, non-purified diet largely prevented diabetes in non-obese diabetic (NOD) mice. In this study we tested hypothesis that early introduction of gluten-enriched (gluten+) diet may increase diabetes incidence in NOD mice.
Standard, gluten-free, gluten+ modified Altromin diets and hydrolysed-casein-based Pregestimil diet were fed to NOD females and diabetes incidence was followed for 310 days. Insulitis score and numbers of gut mucosal lymphocytes were determined in non-diabetic animals.
A significantly lower diabetes incidence (p < 0.0001) was observed in NOD mice fed gluten-free diet (5.9%, n = 34) and Pregestimil diet (10%, n = 30) compared to mice on the standard Altromin diet (60.6%, n = 33). Surprisingly, gluten+ diet also prevented diabetes incidence, even at the level found with the gluten-free diet (p < 0.0001, 5.9%, n = 34). The minority of mice, which developed diabetes on all the three diabetes-protective (gluten+, gluten-free, Pregestimil) diets, did that slightly later compared to those on the standard diet. Lower insulitis score compared to control mice was found in non-diabetic NOD mice on the gluten-free, and to a lesser extent also gluten+ and Pregestimil diets. No substantial differences in the number of CD3(+), TCR-gammadelta(+), and IgA(+) cells in the small intestine were documented.
Gluten+ diet prevents diabetes in NOD mice at the level found with the non-purified gluten-free diet. Possible mechanisms of the enigmatic, dual effect of dietary gluten on the development of T1D are discussed.
营养或感染暴露等环境因素在1型糖尿病(T1D)的发病机制中起着重要作用。我们之前已经表明,无麸质、未纯化的饮食在很大程度上预防了非肥胖糖尿病(NOD)小鼠患糖尿病。在本研究中,我们检验了早期引入富含麸质(麸质+)饮食可能增加NOD小鼠糖尿病发病率的假设。
将标准、无麸质、麸质+改良的Altromin饮食和基于水解酪蛋白的Pregestimil饮食喂给NOD雌性小鼠,并跟踪310天的糖尿病发病率。在非糖尿病动物中测定胰岛炎评分和肠道黏膜淋巴细胞数量。
与食用标准Altromin饮食的小鼠(60.6%,n = 33)相比,食用无麸质饮食(5.9%,n = 34)和Pregestimil饮食(10%,n = 30)的NOD小鼠糖尿病发病率显著降低(p < 0.0001)。令人惊讶的是,麸质+饮食也预防了糖尿病的发生,甚至达到了无麸质饮食的预防水平(p < 0.0001,5.9%,n = 34)。在所有三种具有糖尿病预防作用(麸质+、无麸质、Pregestimil)的饮食中发生糖尿病的少数小鼠,与食用标准饮食的小鼠相比,发病时间稍晚。与对照小鼠相比,食用无麸质饮食以及在较小程度上食用麸质+和Pregestimil饮食的非糖尿病NOD小鼠胰岛炎评分较低。在小肠中,CD3(+)、TCR-γδ(+)和IgA(+)细胞数量没有显著差异。
麸质+饮食在非纯化无麸质饮食的预防水平上预防了NOD小鼠患糖尿病。本文讨论了膳食麸质对T1D发展产生神秘双重作用的可能机制。