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约氏乳杆菌 N6.2 可减轻 BB-DP 大鼠 1 型糖尿病的发展。

Lactobacillus johnsonii N6.2 mitigates the development of type 1 diabetes in BB-DP rats.

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville, Florida, United States of America.

出版信息

PLoS One. 2010 May 6;5(5):e10507. doi: 10.1371/journal.pone.0010507.

Abstract

BACKGROUND

The intestinal epithelium is a barrier that composes one of the most immunologically active surfaces of the body due to constant exposure to microorganisms as well as an infinite diversity of food antigens. Disruption of intestinal barrier function and aberrant mucosal immune activation have been implicated in a variety of diseases within and outside of the gastrointestinal tract. With this model in mind, recent studies have shown a link between diet, composition of intestinal microbiota, and type 1 diabetes pathogenesis. In the BioBreeding rat model of type 1 diabetes, comparison of the intestinal microbial composition of diabetes prone and diabetes resistant animals found Lactobacillus species were negatively correlated with type 1 diabetes development. Two species, Lactobacillus johnsonii and L. reuteri, were isolated from diabetes resistant rats. In this study diabetes prone rats were administered pure cultures of L. johnsonii or L. reuteri isolated from diabetes resistant rats to determine the effect on type 1 diabetes development.

METHODOLOGY/PRINCIPAL: Findings Results Rats administered L. johnsonii, but not L. reuteri, post-weaning developed type 1 diabetes at a protracted rate. Analysis of the intestinal ileum showed administration of L. johnsonii induced changes in the native microbiota, host mucosal proteins, and host oxidative stress response. A decreased oxidative intestinal environment was evidenced by decreased expression of several oxidative response proteins in the intestinal mucosa (Gpx1, GR, Cat). In L. johnsonii fed animals low levels of the pro-inflammatory cytokine IFNgamma were correlated with low levels of iNOS and high levels of Cox2. The administration of L. johnsonii also resulted in higher levels of the tight junction protein claudin.

CONCLUSIONS

It was determined that the administration of L. johnsonii isolated from BioBreeding diabetes resistant rats delays or inhibits the onset of type 1 diabetes in BioBreeding diabetes prone rats. Taken collectively, these data suggest that the gut and the gut microbiota are potential agents of influence in type 1 diabetes development. These data also support therapeutic efforts that seek to modify gut microbiota as a means to modulate development of this disorder.

摘要

背景

肠道上皮是构成身体最具免疫活性表面之一的屏障,因为它会不断暴露于微生物和无限多样的食物抗原中。肠道屏障功能的破坏和黏膜免疫的异常激活与胃肠道内外的多种疾病有关。考虑到这种模式,最近的研究表明饮食、肠道微生物组成和 1 型糖尿病发病机制之间存在联系。在 1 型糖尿病的生物繁殖大鼠模型中,比较易患糖尿病和不易患糖尿病动物的肠道微生物组成发现,乳杆菌属与 1 型糖尿病的发展呈负相关。从不易患糖尿病的大鼠中分离出两种乳杆菌,即约翰逊乳杆菌和雷特氏乳杆菌。在这项研究中,易患糖尿病的大鼠被给予从不易患糖尿病的大鼠中分离出的纯培养约翰逊乳杆菌或雷特氏乳杆菌,以确定其对 1 型糖尿病发展的影响。

方法/原理:研究结果表明,断奶后给予约翰逊乳杆菌但不给雷特氏乳杆菌的大鼠以延长的速度发展为 1 型糖尿病。对回肠的分析表明,给予约翰逊乳杆菌会改变本地微生物群、宿主黏膜蛋白和宿主氧化应激反应。肠道环境的氧化减少表现为肠道黏膜中几种氧化反应蛋白的表达减少(Gpx1、GR、Cat)。在给予约翰逊乳杆菌的动物中,促炎细胞因子 IFNγ 的低水平与 iNOS 的低水平和 Cox2 的高水平相关。给予约翰逊乳杆菌也导致紧密连接蛋白 Claudin 的水平升高。

结论

从生物繁殖糖尿病抗性大鼠中分离出的约翰逊乳杆菌的给予延迟或抑制了生物繁殖糖尿病易发性大鼠 1 型糖尿病的发病。总的来说,这些数据表明肠道和肠道微生物群可能是 1 型糖尿病发展的影响因素。这些数据还支持了寻求改变肠道微生物群作为调节这种疾病发展的方法的治疗努力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/793d/2865539/0579dac40caf/pone.0010507.g001.jpg

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