Shenqi compound ameliorates type-2 diabetes mellitus by modulating the gut microbiota and metabolites

肠道菌群 代谢组学 厚壁菌 蔷薇花 2型糖尿病 拟杆菌 血糖性 化学 拟杆菌 肠道通透性 胰岛素抵抗 生物化学 糖尿病 生物 药理学 微生物学 免疫学 细菌 内分泌学 生物信息学 16S核糖体RNA 基因 遗传学
作者
Xiyu Zhang,Heting Wang,Chunguang Xie,Zhipeng Hu,Yuan Zhang,Sihan Peng,Yuchi He,Jian Kang,Hong Gao,Haipo Yuan,Ya Liu,Gang Fan
出处
期刊:Journal of Chromatography B [Elsevier]
卷期号:1194: 123189-123189 被引量:23
标识
DOI:10.1016/j.jchromb.2022.123189
摘要

The gut microbiota (GM) and metabolites are important factors in mediating the development of type-2 diabetes mellitus (T2DM). An imbalance in the gut microbiota and metabolites can disrupt the function of the intestinal barrier, cause changes in the permeability of the intestinal mucosa and promote the immune inflammatory response, thereby aggravating the fluctuation of blood glucose level and promoting the occurrence and development of the chronic complications of DM. Manipulating the GM and metabolites is a promising therapeutic intervention and is being studied extensively. Shenqi compound (SQC) is a traditional Chinese medicine formulation, which has been widely used to improve T2DM. Studies have demonstrated that SQC can reduce glycemic variability, alleviate the inflammatory response, etc. However, its underlying mechanism remains unknown. Therefore, in this experiment, We administered SQC to Goto-Kakizaki (GK) rats and evaluated its effect on blood glucose homeostasis and the intestinal mucosal barrier. We identified the profiles of the GM and metabolites with the aid of 16S rDNA gene sequencing and non-target metabolomics analysis. It showed that SQC intervention could reduce glycemic variability, regulate serum levels of glucagon and insulin, and improve injury to the intestinal mucosal barrier of GK rats. In the gut, the ratio of bacteria of the phyla Bacteroidetes/Firmicutes could be improved after SQC intervention. SQC also regulated the relative abundance of Prevotellaceae, Butyricimonas, Bacteroides, Blautia, Roseburia, Lactobacillus, and Rothia. We found out that expression of 40 metabolites was significantly improved after SQC intervention. Further analyses of metabolic pathways indicated that the therapeutic effect of SQC might be related predominantly to its ability to improve gluconeogenesis/glycolysis, amino acid metabolism, lipid metabolism, citrate cycle, and butanoate metabolism. These results suggest that SQC may exert a beneficial role in T2DM by modulating the GM and metabolites in different pathways.
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