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本文引用的文献

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A metagenome-wide association study of gut microbiota in type 2 diabetes.2 型糖尿病患者肠道微生物组的宏基因组关联研究。
Nature. 2012 Oct 4;490(7418):55-60. doi: 10.1038/nature11450. Epub 2012 Sep 26.
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The regulation of food intake by the gut-brain axis: implications for obesity.肠道-脑轴对摄食的调节:肥胖的影响。
Int J Obes (Lond). 2013 May;37(5):625-33. doi: 10.1038/ijo.2012.93. Epub 2012 Jun 19.
3
Probiotics, their health benefits and applications for developing healthier foods: a review.益生菌、其健康益处以及在开发更健康食品中的应用:综述。
FEMS Microbiol Lett. 2012 Sep;334(1):1-15. doi: 10.1111/j.1574-6968.2012.02593.x. Epub 2012 May 28.
4
Butyrate and propionate protect against diet-induced obesity and regulate gut hormones via free fatty acid receptor 3-independent mechanisms.丁酸盐和丙酸盐通过游离脂肪酸受体 3 非依赖性机制预防饮食诱导的肥胖和调节肠道激素。
PLoS One. 2012;7(4):e35240. doi: 10.1371/journal.pone.0035240. Epub 2012 Apr 10.
5
Gut microbiota is a key modulator of insulin resistance in TLR 2 knockout mice.肠道微生物群是 TLR2 敲除小鼠胰岛素抵抗的关键调节因子。
PLoS Biol. 2011 Dec;9(12):e1001212. doi: 10.1371/journal.pbio.1001212. Epub 2011 Dec 6.
6
Brain-derived neurotrophic factor, food intake regulation, and obesity.脑源性神经营养因子、摄食调节与肥胖。
Arch Med Res. 2011 Aug;42(6):482-94. doi: 10.1016/j.arcmed.2011.09.005. Epub 2011 Sep 22.
7
Health benefits and health claims of probiotics: bridging science and marketing.益生菌的健康益处和健康声称:连接科学和营销。
Br J Nutr. 2011 Nov;106(9):1291-6. doi: 10.1017/S000711451100287X. Epub 2011 Aug 24.
8
Targeting gut microbiota in obesity: effects of prebiotics and probiotics.靶向肥胖症中的肠道微生物群:益生元和益生菌的作用。
Nat Rev Endocrinol. 2011 Aug 9;7(11):639-46. doi: 10.1038/nrendo.2011.126.
9
Inflammation-mediated obesity and insulin resistance as targets for nutraceuticals.炎症介导的肥胖和胰岛素抵抗作为营养保健品的作用靶点。
Ann N Y Acad Sci. 2011 Jul;1229:140-6. doi: 10.1111/j.1749-6632.2011.06098.x.
10
Gut microbiota interactions with obesity, insulin resistance and type 2 diabetes: did gut microbiote co-evolve with insulin resistance?肠道微生物群与肥胖、胰岛素抵抗和 2 型糖尿病的相互作用:肠道微生物群是否与胰岛素抵抗共同进化?
Curr Opin Clin Nutr Metab Care. 2011 Sep;14(5):483-90. doi: 10.1097/MCO.0b013e328348c06d.

通过丁酸诱导 GLP-1 激素分泌来实现益生菌的有益代谢作用。

Beneficial metabolic effects of a probiotic via butyrate-induced GLP-1 hormone secretion.

机构信息

From the Diabetes, Endocrinology, and Obesity Branch.

the Laboratory of Biological Chemistry, and.

出版信息

J Biol Chem. 2013 Aug 30;288(35):25088-25097. doi: 10.1074/jbc.M113.452516. Epub 2013 Jul 8.

DOI:10.1074/jbc.M113.452516
PMID:23836895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3757173/
Abstract

Obesity and diabetes are associated with excess caloric intake and reduced energy expenditure resulting in a negative energy balance. The incidence of diabetes has reached epidemic proportions, and childhood diabetes and obesity are increasing alarmingly. Therefore, it is important to develop safe, easily deliverable, and economically viable treatment alternatives for these diseases. Here, we provide data supporting the candidacy of probiotics as such a therapeutic modality against obesity and diabetes. Probiotics are live bacteria that colonize the gastrointestinal tract and impart beneficial effects for health. However, their widespread prescription as medical therapies is limited primarily because of the paucity of our understanding of their mechanism of action. Here, we demonstrate that the administration of a probiotic, VSL#3, prevented and treated obesity and diabetes in several mouse models. VSL#3 suppressed body weight gain and insulin resistance via modulation of the gut flora composition. VSL#3 promoted the release of the hormone GLP-1, resulting in reduced food intake and improved glucose tolerance. The VSL#3-induced changes were associated with an increase in the levels of a short chain fatty acid (SCFA), butyrate. Using a cell culture system, we demonstrate that butyrate stimulated the release of GLP-1 from intestinal L-cells, thereby providing a plausible mechanism for VSL#3 action. These findings suggest that probiotics such as VSL#3 can modulate the gut microbiota-SCFA-hormone axis. Moreover, our results indicate that probiotics are of potential therapeutic utility to counter obesity and diabetes.

摘要

肥胖症和糖尿病与热量摄入过多和能量消耗减少有关,导致能量负平衡。糖尿病的发病率已达到流行程度,儿童糖尿病和肥胖症的发病率令人震惊地上升。因此,开发安全、易于实施和经济可行的治疗这些疾病的替代方法非常重要。在这里,我们提供的数据支持益生菌作为治疗肥胖症和糖尿病的一种治疗方法。益生菌是定植于胃肠道并产生有益健康影响的活菌。然而,它们作为医疗疗法的广泛应用主要受到我们对其作用机制的理解有限的限制。在这里,我们证明了益生菌 VSL#3 在几种小鼠模型中预防和治疗肥胖症和糖尿病。VSL#3 通过调节肠道菌群组成来抑制体重增加和胰岛素抵抗。VSL#3 促进了激素 GLP-1 的释放,导致食物摄入量减少和葡萄糖耐量改善。VSL#3 诱导的变化与短链脂肪酸 (SCFA) 丁酸水平的增加有关。使用细胞培养系统,我们证明丁酸刺激肠 L 细胞释放 GLP-1,从而为 VSL#3 作用提供了一个合理的机制。这些发现表明,益生菌(如 VSL#3)可以调节肠道微生物群-SCFA-激素轴。此外,我们的结果表明,益生菌具有治疗肥胖症和糖尿病的潜在治疗作用。