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桑椹多糖通过调节肠道微生物群和肠道屏障对 TLR4/NF-κB 通路缓解糖尿病症状。

Fructus mori polysaccharide alleviates diabetic symptoms by regulating intestinal microbiota and intestinal barrier against TLR4/NF-κB pathway.

机构信息

Guangdong Province Key Laboratory for Green Processing of Natural Products and Product Safety, Guangzhou 510640, China; SCUT-Zhuhai Institute of Modern Industrial Innovation, School of Food Science and Engineering, South China University of Technology, 381 Wushan Road, Guangzhou 510640, China.

Guangzhou Wondfo Health Science and Technology Co., Ltd, China.

出版信息

Int J Biol Macromol. 2023 Sep 30;249:126038. doi: 10.1016/j.ijbiomac.2023.126038. Epub 2023 Jul 27.

Abstract

Fructus mori polysaccharide (FMP) has a variety of biological activities. In this study, the results showed that FMP alleviated hyperglycemia, insulin resistance, hyperlipidemia, endotoxemia, and high metabolic inflammation levels in type 2 diabetic (T2DM) mice. Next, it was found that the above beneficial effects of FMP on diabetic mice were significantly attenuated after antibiotics eliminated intestinal microbiota (IM) of mice. In addition, FMP suppressed intestinal inflammation and oxidative stress levels by inhibiting the activation of the TLR4/MyD88/NF-κB pathway, and indirectly upregulated the expression of the tight junction proteins Claudin-1, Occludin, and Zonula occlusionn-1 (ZO-1) to repair the intestinal barrier. Interestingly, the protective effect of FMP on the intestinal barrier was also attributed to its regulation of IM. The 16S rRNA and Spearman correlation analysis showed that FMP could repair the intestinal barrier to improve T2DM by remodeling specific IM, especially by significantly inhibiting 93.66 % of endotoxin-producing Shigella and promoting the proliferation of probiotic Allobaculum and Bifidobacterium by 16.31 % and 19.07 %, respectively. This study provided a theoretical support for the application of FMP as a novel probiotic in functional foods for diabetes.

摘要

桑椹多糖(FMP)具有多种生物活性。本研究表明,FMP 可缓解 2 型糖尿病(T2DM)小鼠的高血糖、胰岛素抵抗、高血脂、内毒素血症和高代谢炎症水平。接下来发现,抗生素消除小鼠肠道菌群(IM)后,FMP 对糖尿病小鼠的上述有益作用明显减弱。此外,FMP 通过抑制 TLR4/MyD88/NF-κB 通路的激活,抑制肠道炎症和氧化应激水平,间接上调紧密连接蛋白 Claudin-1、Occludin 和 Zonula Occlusionn-1(ZO-1)的表达,修复肠道屏障。有趣的是,FMP 对肠道屏障的保护作用也归因于其对 IM 的调节。16S rRNA 和 Spearman 相关分析表明,FMP 可以通过重塑特定的 IM 来修复肠道屏障,从而改善 T2DM,特别是通过显著抑制 93.66%的产内毒素志贺氏菌,并分别促进益生菌 Allobaculum 和双歧杆菌的增殖 16.31%和 19.07%。本研究为 FMP 作为一种新型益生菌在糖尿病功能性食品中的应用提供了理论支持。

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