G蛋白偶联胆汁酸受体                        
                
                                
                        
                            肠道菌群                        
                
                                
                        
                            胆汁酸                        
                
                                
                        
                            生物                        
                
                                
                        
                            拟杆菌                        
                
                                
                        
                            产热                        
                
                                
                        
                            新陈代谢                        
                
                                
                        
                            脂肪组织                        
                
                                
                        
                            生物化学                        
                
                                
                        
                            褐色脂肪组织                        
                
                                
                        
                            内分泌学                        
                
                                
                        
                            细菌                        
                
                                
                        
                            遗传学                        
                
                        
                    
            作者
            
                Bingting Chen,Yu Bai,Fenglian Tong,Junlin Yan,Rui Zhang,Yewei Zhong,Huiwen Tan,Xiaoli Ma            
         
                    
            出处
            
                                    期刊:Gut microbes
                                                         [Landes Bioscience]
                                                        日期:2023-03-26
                                                        卷期号:15 (1)
                                                        被引量:75
                                 
         
        
    
            
            标识
            
                                    DOI:10.1080/19490976.2023.2192155
                                    
                                
                                 
         
        
                
            摘要
            
            Accumulating evidence suggests that the bile acid regulates type 2 diabetes mellitus (T2DM) through gut microbiota-host interactions. However, the mechanisms underlying such interactions have been unclear. Here, we found that glycoursodeoxycholic acid (GUDCA) positively regulates gut microbiota by altering bile acid metabolism. GUDCA in mice resulted in higher taurolithocholic acid (TLCA) level and Bacteroides vulgatus abundance. Together, these changes resulted in the activation of the adipose G-protein-coupled bile acid receptor, GPBAR1 (TGR5) and upregulated expression of uncoupling protein UCP-1, resulting in elevation of white adipose tissue thermogenesis. The anti-T2DM effects of GUDCA are linked with the regulation of the bile acid and gut microbiota composition. This study suggests that altering bile acid metabolism, modifying the gut microbiota may be of value for the treatment of T2DM.
         
            
 
                 
                
                    
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