Antidiabetic Effects of Gegen Qinlian Decoction via the Gut Microbiota are Attributable to Its Key Ingredient Berberine

被引:39
作者
Xu, Xizhan [1 ,2 ]
Gao, Zezheng [3 ,4 ]
Yang, Fuquan [5 ,6 ]
Yang, Yingying [3 ,4 ]
Chen, Liang [1 ]
Han, Lin [3 ]
Zhao, Na [1 ]
Xu, Jiayue [1 ]
Wang, Xinmiao [3 ]
Ma, Yue [1 ,2 ]
Shu, Lian [2 ,5 ,6 ]
Hu, Xiaoxi [1 ]
Lyu, Na [1 ]
Pan, Yuanlong [1 ]
Zhu, Baoli [1 ]
Zhao, Linhua [3 ]
Tong, Xiaolin [3 ,7 ]
Wang, Jun [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] China Acad Chinese Med Sci, Guanganmen Hosp, Dept Endocrinol, Beijing 100053, Peoples R China
[4] Beijing Univ Chinese Med, Beijing 100029, Peoples R China
[5] Chinese Acad Sci, Inst Biophys, Lab Prot & Peptide Pharmaceut, Beijing 100101, Peoples R China
[6] Chinese Acad Sci, Inst Biophys, Lab Prote, Beijing 100101, Peoples R China
[7] Guangzhou Univ Chinese Med, Shenzhen Hosp, Shenzhen 518034, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Gut microbiota; Type 2 diabetes mellitus; Traditional Chinese medicine; Berberine; Gegen Qinlian Decoction; METFORMIN ALTERS; TYPE-2; BUTYRATE; GLUCOSE; THERMOGENESIS; INFLAMMATION; HOMEOSTASIS; ACTIVATION; METAGENOME; OBESITY;
D O I
10.1016/j.gpb.2019.09.007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gegen Qinlian Decoction (GQD), a traditional Chinese medicine (TCM) formula, has long been used for the treatment of common metabolic diseases, including type 2 diabetes mellitus. However, the main limitation of its wider application is ingredient complexity of this formula. Thus, it is critically important to identify the major active ingredients of GQD and to illustrate mechanisms underlying its action. Here, we compared the effects of GQD and berberine, a hypothetical key active pharmaceutical ingredient of GQD, on a diabetic rat model by comprehensive analyses of gut microbiota, short-chain fatty acids, proinflammatory cytokines, and ileum transcriptomics. Our results show that berberine and GQD had similar effects on lowering blood glucose levels, modulating gut microbiota, inducing ileal gene expression, as well as relieving systemic and local inflammation. As expected, both berberine and GQD treatment significantly altered the overall gut microbiota structure and enriched many butyrate-producing bacteria, including Faecalibacterium and Roseburia, thereby attenuating intestinal inflammation and lowering glucose. Levels of short-chain fatty acids in rat feces were also significantly elevated after treatment with berberine or GQD. Moreover, concentration of serum proinflammatory cytokines and expression of immune-related genes, including Nfkb1, Stat1, and Ifnrg1, in pancreatic islets were significantly reduced after treatment. Our study demonstrates that the main effects of GQD can be attributed to berberine via modulating gut microbiota. The strategy employed would facilitate further standardization and widespread application of TCM in many diseases.
引用
收藏
页码:721 / 736
页数:16
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