Mulberry leaf polysaccharides ameliorate glucose and lipid metabolism disorders via the gut microbiota-bile acids metabolic pathway

被引:0
|
作者
Dai, Hongyu [1 ,3 ]
Shan, Ziyi [2 ]
Shi, Lu [1 ,4 ]
Duan, Yuhui [1 ]
An, Yongcheng [1 ]
He, Changhao [1 ]
Lyu, Yinglan [5 ]
Zhao, Yige [1 ]
Wang, Menglu [1 ]
Du, Yuhang [1 ]
Xie, Jiamei [1 ]
Yang, Yang [1 ]
Zhao, Baosheng [6 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing 100029, Peoples R China
[2] Beijing Univ Chinese Med, Sch Life Sci, Beijing 100029, Peoples R China
[3] Yaan Peoples Hosp, Operat & Management Dept, Yaan 625099, Peoples R China
[4] Qingdao Municipal Hosp, Cent Labs, Qingdao 266011, Peoples R China
[5] Beijing Univ Chinese Med, Coll Chinese Med, Beijing 100029, Peoples R China
[6] Beijing Univ Chinese Med, Beijing Res Inst Chinese Med, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Gut microbiota; Bile acids; Mulberry leaf polysaccharides; INSULIN-RESISTANCE; SALT HYDROLASE; DEFICIENCY; SEQUENCES; MICE; AXIS;
D O I
10.1016/j.ijbiomac.2024.136876
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mulberry leaf polysaccharides (MLP) are integral components of Mulberry leaves that confer hypoglycemic and hypolipidemic properties. This study investigated the efficacy of MLP in treating Type 2 Diabetes Mellitus (T2DM) and the underlying mechanisms related to gut microbiota-bile acids metabolism in T2DM rats. The findings revealed that MLP apparently reduced fasting blood glucose and lipid levels, ameliorated disorders in glucose and lipid metabolism, and mitigated insulin resistance. MLP enhanced the abundance of Prevotella, Ruminococcus, and Lactobacillus, thereby rectifying the gut microbiota dysbiosis in rats, which effectively restored gut microbiota homeostasis and composition. Furthermore, the data demonstrated that MLP modulated bile acid metabolism, as evidenced by reduced serum cholesterol levels, enhanced mRNA expression of hepatic cholesterol 7 alpha- hydroxylase (Cyp7a1) and cholesterol 12 alpha- hydroxylase (Cyp8b1), and ileal G protein-coupled bile acid receptor ( Tgr5) , while suppressing hepatic and ileal farnesoid X receptor (Fxr) mRNA expression in T2DM rats. Additionally, MLP upregulated the protein expression of hepatic CYP7A1 and CYP8B1, and ileal TGR5, while inhibiting FXR protein levels in the liver and ileum of T2DM rats. These results suggest that MLP can rectify disorders in glucose and lipid metabolism via the gut microbiota-bile acids metabolic pathway.
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页数:17
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