Ge-Gen-Jiao-Tai-Wan Affects Type 2 Diabetic Rats by Regulating Gut Microbiota and Primary Bile Acids

被引:14
|
作者
Chen, Han [1 ,2 ]
Yao, Ye [1 ,2 ]
Wang, Wenbo [1 ,2 ]
Wang, Dongsheng [1 ,2 ]
机构
[1] Cent South Univ, Inst Integrated Tradit Chinese & Western Med, Xiangya Hosp, Changsha 410008, Peoples R China
[2] Cent South Univ, Hunan Key Lab Tradit Chinese Med Gan State Adm, Changsha 410008, Peoples R China
关键词
LACTOBACILLUS; RECEPTOR; POPULATION; MODULATION; MECHANISMS; SIGNATURES; METFORMIN; MEDICINE; OBESITY; GLP-1;
D O I
10.1155/2021/5585952
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
The Ge-Gen-Jiao-Tai-Wan (GGJTW) formula has been used to treat type 2 diabetes mellitus (T2DM) in China for a long time. Our previous study has proved that GGJTW could alleviate the type 2 diabetic symptoms, but the underlying mechanisms are still unclear. This study aimed to investigate the changes in gut microbiota and primary bile acids (PBAs) to determine the potential mechanisms of GGJTW in treating T2DM.The fecal transplant method and pseudogerm-free rats were used in our study.The16S rRNA gene sequencing method was used to analyze the changes in the intestinal flora, and PBAs in the colon contents were detected. Finally, the expression of farnesoid X receptor (FXR), G protein-coupled membrane receptor 5 (TGR5), and glucagon-like peptide-1 (GLP-1) was assessed. Following GGJTW treatment, we observed a decrease in blood glucose levels and improvements in glucose tolerance and serum lipid levels. Furthermore, we found that GGJTW could regulate the composition of the gut microbiota and upregulate the diabetic beneficial phylum Firmicutes and bile-acid-related genus Lactobacillus. PBAs in the colon contents were increased in the GGJTW-treated group, accompanied by upregulated expression of the bile acid receptors FXR and TGR5 and increased concentrations of GLP-1. These results indicated that GGJTW could alleviate symptoms of type 2 diabetic rats by regulating the gut microbiota, promoting the production of PBAs, and upregulating the PBA-FXR/TGR5-GLP-1 pathway.
引用
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页数:13
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