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子实体多糖可缓解2型糖尿病小鼠的高血糖和高血脂,调节肠道菌群。

fruit body polysaccharide alleviates hyperglycemia and hyperlipidemia modulating intestinal microflora in type 2 diabetic mice.

作者信息

Huang Zi-Rui, Huang Qi-Zhen, Chen Ke-Wen, Huang Zi-Feng, Liu Yun, Jia Rui-Bo, Liu Bin

机构信息

College of Food Science, Fujian Agriculture and Forestry University, Fuzhou, China.

Chaozhou Branch of Chemistry and Chemical Engineering Guangdong Laboratory, Chaozhou, China.

出版信息

Front Nutr. 2022 Oct 17;9:1013466. doi: 10.3389/fnut.2022.1013466. eCollection 2022.

Abstract

The disease of type 2 diabetes mellitus (T2DM) is principally induced by insufficient insulin secretion and insulin resistance. In the current study, fruit body polysaccharide (SVP) was prepared and structurally characterized. It was shown that the yield of SVP was 1.91%, and SVP mainly contains small molecular weight polysaccharides. Afterward, the hypoglycemic and hypolipidemic effects and the potential mechanism of SVP in T2DM mice were investigated. The results exhibited oral SVP could reverse the body weight loss, high levels of blood glucose, insulin resistance, hyperlipidemia, and inflammation in T2DM mice. Oral SVP increased fecal short-chain fatty acids (SCFAs) concentrations of T2DM mice. Additionally, 16S rRNA sequencing analysis illustrated that SVP can modulate the structure and function of intestinal microflora in T2DM mice, indicating as decreasing the levels of Firmicutes/Bacteroidetes, , , and increasing the levels of , , and . Additionally, the levels of predicted metabolic functions of Citrate cycle, GABAergic synapse, Insulin signaling pathway were increased, and those of Purine metabolism, Taurine and hypotaurine metabolism, and Starch and sucrose metabolism were decreased in intestinal microflora after SVP treatment. These findings demonstrate that SVP could potentially play hypoglycemic and hypolipidemic effects by regulating gut microflora and be a promising nutraceutical for ameliorating T2DM.

摘要

2型糖尿病(T2DM)主要由胰岛素分泌不足和胰岛素抵抗引起。在本研究中,制备了子实体多糖(SVP)并对其结构进行了表征。结果表明,SVP的得率为1.91%,且SVP主要包含小分子多糖。随后,研究了SVP对T2DM小鼠的降血糖和降血脂作用及其潜在机制。结果显示,口服SVP可逆转T2DM小鼠的体重减轻、高血糖、胰岛素抵抗、高脂血症和炎症。口服SVP可提高T2DM小鼠粪便中短链脂肪酸(SCFAs)的浓度。此外,16S rRNA测序分析表明,SVP可调节T2DM小鼠肠道微生物群的结构和功能,表现为降低厚壁菌门/拟杆菌门的水平,以及增加 、 和 的水平。此外,SVP处理后,肠道微生物群中柠檬酸循环、GABA能突触、胰岛素信号通路的预测代谢功能水平升高,而嘌呤代谢、牛磺酸和低牛磺酸代谢以及淀粉和蔗糖代谢的水平降低。这些发现表明,SVP可能通过调节肠道微生物群发挥降血糖和降血脂作用,有望成为改善T2DM的营养保健品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8434/9632624/12a1c0e38807/fnut-09-1013466-g001.jpg

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