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硫化氢和硫酸盐益生元刺激雄性小鼠体内胰高血糖素样肽-1的分泌并改善血糖水平。

Hydrogen Sulfide and Sulfate Prebiotic Stimulates the Secretion of GLP-1 and Improves Glycemia in Male Mice.

作者信息

Pichette Jennifer, Fynn-Sackey Nancy, Gagnon Jeffrey

机构信息

Laurentian University, Department of Biology, Sudbury, Ontario P3E 2C6, Canada.

出版信息

Endocrinology. 2017 Oct 1;158(10):3416-3425. doi: 10.1210/en.2017-00391.

Abstract

Recently, the gastrointestinal microbiome, and its metabolites, has emerged as a potential regulator of host metabolism. However, to date little is known on the precise mechanisms of how this regulation occurs. Hydrogen sulfide (H2S) is abundantly produced in the colon by sulfate-reducing bacteria (SRB). H2S is a bioactive gas that plays regulatory roles in many systems, including metabolic hormone regulation. This gas metabolite is produced in close proximity to the glucagonlike peptide-1 (GLP-1)-secreting cells in the gut epithelium. GLP-1 is a peptide hormone that plays pivotal roles in both glucose homeostasis and appetite regulation. We hypothesized that H2S can directly regulate GLP-1 secretion. We demonstrated that H2S donors (NaHS and GYY4137) directly stimulate GLP-1 secretion in murine L-cells (GLUTag) and that this occurs through p38 mitogen-activated protein kinase without affecting cell viability. We then increased SRB in mice by supplementing the diet with a prebiotic chondroitin sulfate for 4 weeks. Mice treated with chondroitin sulfate had elevated Desulfovibrio piger levels in the feces and increased colonic and fecal H2S concentration. These animals also had enhanced GLP-1 and insulin secretion, improved oral glucose tolerance, and reduced food consumption. These results indicate that H2S plays a stimulatory role in GLP-1 secretion and that sulfate prebiotics can enhance GLP-1 release and its downstream metabolic actions.

摘要

最近,胃肠道微生物群及其代谢产物已成为宿主代谢的潜在调节因子。然而,迄今为止,对于这种调节发生的精确机制知之甚少。结肠中的硫酸盐还原菌(SRB)大量产生硫化氢(H2S)。H2S是一种生物活性气体,在包括代谢激素调节在内的许多系统中发挥调节作用。这种气体代谢产物在肠道上皮中与分泌胰高血糖素样肽-1(GLP-1)的细胞紧密相邻处产生。GLP-1是一种肽类激素,在葡萄糖稳态和食欲调节中都起着关键作用。我们假设H2S可以直接调节GLP-1的分泌。我们证明,H2S供体(NaHS和GYY4137)直接刺激小鼠L细胞(GLUTag)中的GLP-1分泌,并且这是通过p38丝裂原活化蛋白激酶发生的,而不影响细胞活力。然后,我们通过在小鼠饮食中补充益生元硫酸软骨素4周来增加小鼠体内的SRB。用硫酸软骨素处理的小鼠粪便中脱硫弧菌水平升高,结肠和粪便中的H2S浓度增加。这些动物的GLP-1和胰岛素分泌也增强,口服葡萄糖耐量改善,食物摄入量减少。这些结果表明,H2S在GLP-1分泌中起刺激作用,并且硫酸盐益生元可以增强GLP-1的释放及其下游代谢作用。

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