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苍术多糖通过肠道菌群产生的色氨酸代谢物激活芳香烃受体改善糖脂代谢紊乱。

Atractylodes macrocephala Koidz polysaccharide improves glycolipid metabolism disorders through activation of aryl hydrocarbon receptor by gut flora-produced tryptophan metabolites.

机构信息

College of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.

Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou, China.

出版信息

Int J Biol Macromol. 2023 Dec 31;253(Pt 4):126987. doi: 10.1016/j.ijbiomac.2023.126987. Epub 2023 Sep 18.

DOI:10.1016/j.ijbiomac.2023.126987
PMID:37729987
Abstract

Polysaccharides are known to confer protection against glycolipid metabolism disorders (GMD) by regulating intestinal flora. In this study, a heterogeneous acidic heteropolysaccharide with high molecular weight mainly composed of fructose was isolated from Atractylodes macrocephala Koidz (AMP). Supplementation with AMP was shown to improve diet-induced GMD in a rat model, including decreasing the levels of serum triglycerides, total cholesterol, and glucose, and improving hepatic lipidosis and islet cells morphologies. AMP-treated rats also exhibited modified intestinal flora with enrichments of intestinal Lactobacillus and Rothia species, which was accompanied by increased tryptophan metabolites such as indole-3-propionic acid, indole, tryptamine, and tryptophol. These metabolites promote the expression of intestinal aryl hydrocarbon receptor (AhR) in nuclear fractions. AhR activation increased the expression levels of IL-22 and GLP-1 proteins and mRNA. IL-22 reduced systemic LPS by upregulating the expression of tight junction proteins, antimicrobial peptides, and mucin to ameliorate intestinal barrier function, and activated the hepatic IL-22R/Stat3/Acox1 signaling pathway to improve lipid metabolism. GLP-1 activated the pancreatic GLP-1R/p-CREB signaling pathway to ameliorate β-cell injury and improve insulin resistance. Therefore, the intestinal microbial-tryptophan metabolism-AhR pathway was deduced to be a mechanism by which this polysaccharide improves GMD.

摘要

多糖被认为通过调节肠道菌群来预防糖脂代谢紊乱(GMD)。在这项研究中,从白术(AMP)中分离出一种主要由果糖组成的不均一酸性杂多糖,具有高分子量。AMP 的补充可改善大鼠模型的饮食诱导的 GMD,包括降低血清甘油三酯、总胆固醇和葡萄糖水平,改善肝脂肪变性和胰岛细胞形态。AMP 处理的大鼠还表现出肠道菌群的改变,肠道乳杆菌和罗氏菌增多,伴随着色氨酸代谢物如吲哚-3-丙酸、吲哚、色胺和色醇的增加。这些代谢物促进了肠道芳香烃受体(AhR)在核部分的表达。AhR 激活增加了 IL-22 和 GLP-1 蛋白和 mRNA 的表达水平。IL-22 通过上调紧密连接蛋白、抗菌肽和粘蛋白的表达来减少全身 LPS,从而改善肠道屏障功能,并激活肝脏 IL-22R/Stat3/Acox1 信号通路以改善脂质代谢。GLP-1 激活胰腺 GLP-1R/p-CREB 信号通路,改善 β 细胞损伤,改善胰岛素抵抗。因此,肠道微生物-色氨酸代谢-AhR 途径被推断为该多糖改善 GMD 的机制。

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