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本文引用的文献

1
The effect of Saccharomyces boulardii on human colon cells and inflammation in rats with trinitrobenzene sulfonic acid-induced colitis.布拉氏酵母菌对三硝基苯磺酸诱导的大鼠结肠炎模型中人类结肠细胞及炎症的影响。
Dig Dis Sci. 2009 Feb;54(2):255-63. doi: 10.1007/s10620-008-0357-0. Epub 2008 Jul 10.
2
Probiotic Escherichia coli Nissle 1917 versus placebo for treating diarrhea of greater than 4 days duration in infants and toddlers.益生菌大肠杆菌Nissle 1917与安慰剂治疗婴幼儿持续时间超过4天的腹泻。
Pediatr Infect Dis J. 2008 Jun;27(6):494-9. doi: 10.1097/INF.0b013e318169034c.
3
Probiotics and prebiotics in inflammatory bowel disease: microflora 'on the scope'.炎症性肠病中的益生菌和益生元:微生物区系“在视野范围内”
Br J Clin Pharmacol. 2008 Apr;65(4):453-67. doi: 10.1111/j.1365-2125.2008.03096.x. Epub 2008 Feb 12.
4
Clinical use of E. coli Nissle 1917 in inflammatory bowel disease.大肠杆菌Nissle 1917在炎症性肠病中的临床应用。
Inflamm Bowel Dis. 2008 Jul;14(7):1012-8. doi: 10.1002/ibd.20377.
5
Probiotic Escherichia coli Nissle 1917 inhibits leaky gut by enhancing mucosal integrity.益生菌大肠杆菌Nissle 1917通过增强黏膜完整性来抑制肠道渗漏。
PLoS One. 2007 Dec 12;2(12):e1308. doi: 10.1371/journal.pone.0001308.
6
Molecular fingerprints of neutrophil-dependent oxidative stress in inflammatory bowel disease.炎症性肠病中中性粒细胞依赖性氧化应激的分子指纹图谱。
J Gastroenterol. 2007 Oct;42(10):787-98. doi: 10.1007/s00535-007-2096-y. Epub 2007 Oct 15.
7
The intestinal anti-inflammatory effects of the novel agent UR-1505 in the TNBS model of rat colitis are mediated by T-lymphocyte inhibition.新型药物UR-1505在大鼠结肠炎TNBS模型中的肠道抗炎作用是通过抑制T淋巴细胞介导的。
Biochem Pharmacol. 2007 Nov 15;74(10):1496-506. doi: 10.1016/j.bcp.2007.07.026. Epub 2007 Jul 22.
8
Molecular mechanisms underlying the probiotic effects of Escherichia coli Nissle 1917 involve ZO-2 and PKCzeta redistribution resulting in tight junction and epithelial barrier repair.大肠杆菌Nissle 1917益生菌作用的分子机制涉及ZO-2和PKCζ的重新分布,从而导致紧密连接和上皮屏障修复。
Cell Microbiol. 2007 Mar;9(3):804-16. doi: 10.1111/j.1462-5822.2006.00836.x. Epub 2006 Nov 3.
9
A role for nitric oxide-mediated peroxynitrite formation in a model of endotoxin-induced shock.一氧化氮介导的过氧亚硝酸盐形成在内毒素诱导的休克模型中的作用。
J Pharmacol Exp Ther. 2006 Oct;319(1):73-81. doi: 10.1124/jpet.106.108100. Epub 2006 Jun 30.
10
Escherichia coli strain Nissle 1917 ameliorates experimental colitis via toll-like receptor 2- and toll-like receptor 4-dependent pathways.大肠杆菌菌株Nissle 1917通过Toll样受体2和Toll样受体4依赖性途径改善实验性结肠炎。
Infect Immun. 2006 Jul;74(7):4075-82. doi: 10.1128/IAI.01449-05.

一种益生菌大肠杆菌菌株,即尼尔斯 1917 株,经口服给予可在脂多糖诱导的小鼠脓毒症中发挥局部和全身抗炎作用。

A probiotic strain of Escherichia coli, Nissle 1917, given orally exerts local and systemic anti-inflammatory effects in lipopolysaccharide-induced sepsis in mice.

机构信息

Centro de Investigaciones Biomédicas en Red - Enfermedades Hepáticas y Digestivas (CIBER-EHD), Department of Pharmacology, Center for Biomedical Research, University of Granada, Granada, Spain.

出版信息

Br J Pharmacol. 2009 Jul;157(6):1024-33. doi: 10.1111/j.1476-5381.2009.00270.x. Epub 2009 May 26.

DOI:10.1111/j.1476-5381.2009.00270.x
PMID:19486007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2737661/
Abstract

BACKGROUND AND PURPOSE

Escherichia coli Nissle 1917 is a probiotic strain used in the treatment of intestinal immune diseases, including ulcerative colitis. The aim of the present study was to test if this probiotic bacterium can also show systemic immunomodulatory properties after oral administration.

EXPERIMENTAL APPROACH

The probiotic strain was administered to rats or mice for 2 weeks before its assay in two experimental models of altered immune response, the trinitrobenzenesulphonic acid (TNBS) model of rat colitis, localized in the colon, and the lipopolysaccharide (LPS) model of systemic septic shock in mice. Inflammatory status was evaluated both macroscopically and biochemically after 1 week in the TNBS model or after 24 h in the LPS shock model. In addition, splenocytes were obtained from mice and stimulated, ex vivo, with concanavalin A or LPS to activate T or B cells, respectively, and cytokine production (IL-2, IL-5 and IL-10) by T cells and IgG secretion by B cells measured.

KEY RESULTS

E. coli Nissle 1917 was anti-inflammatory in both models of altered immune response. This included a reduction in the pro-inflammatory cytokine tumour necrosis factor-alpha both in the intestine from colitic rats, and in plasma and lungs in mice treated with LPS. The systemic beneficial effect was associated with inhibited production of the T cell cytokines and by down-regulation of IgG release from splenocyte-derived B cells.

CONCLUSIONS AND IMPLICATIONS

The anti-inflammatory effects of E. coli Nissle 1917 given orally were not restricted to the gastrointestinal tract.

摘要

背景与目的

大肠杆菌 Nissle 1917 是一种益生菌菌株,用于治疗包括溃疡性结肠炎在内的肠道免疫疾病。本研究旨在测试该益生菌菌株经口服给药后是否还具有全身免疫调节特性。

实验方法

在两种免疫反应改变的实验模型中,即局部在结肠的三硝基苯磺酸(TNBS)大鼠结肠炎模型和小鼠全身败血症性休克的脂多糖(LPS)模型中,对益生菌菌株进行 2 周的给药,然后对其进行检测。在 TNBS 模型中 1 周后或 LPS 休克模型中 24 小时后,分别从大鼠和小鼠中获取脾细胞,并用刀豆球蛋白 A 或 LPS 进行体外刺激,分别激活 T 细胞或 B 细胞,并测量 T 细胞的细胞因子(IL-2、IL-5 和 IL-10)产生和 B 细胞的 IgG 分泌。

主要结果

大肠杆菌 Nissle 1917 在两种免疫反应改变的模型中均具有抗炎作用。这包括减少结肠炎大鼠肠道中促炎细胞因子肿瘤坏死因子-α的产生,以及 LPS 处理的小鼠血浆和肺中该因子的产生。全身有益作用与 T 细胞细胞因子产生的抑制以及脾细胞来源的 B 细胞 IgG 释放的下调有关。

结论与意义

经口服给予大肠杆菌 Nissle 1917 的抗炎作用不仅局限于胃肠道。