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            
         
                    
        
    
            
            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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