CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Department of Endocrinology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing 100053, China; Beijing University of Chinese Medicine, Beijing 100029, China.
Genomics Proteomics Bioinformatics. 2020 Dec;18(6):721-736. doi: 10.1016/j.gpb.2019.09.007. Epub 2020 Dec 24.
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.
针对秦连解毒汤(GQD),一种传统的中药(TCM)配方,长期以来一直用于治疗常见的代谢疾病,包括 2 型糖尿病。然而,其更广泛应用的主要限制是该配方的成分复杂性。因此,确定 GQD 的主要活性成分并阐明其作用机制至关重要。在这里,我们通过综合分析肠道微生物群、短链脂肪酸、促炎细胞因子和回肠转录组学,比较了 GQD 和黄连素(GQD 的假定主要活性药物成分)对糖尿病大鼠模型的影响。我们的结果表明,黄连素和 GQD 对降低血糖水平、调节肠道微生物群、诱导回肠基因表达以及缓解全身和局部炎症具有相似的作用。正如预期的那样,黄连素和 GQD 治疗均显著改变了肠道微生物群的整体结构,并丰富了许多产生丁酸盐的细菌,包括粪杆菌和罗氏菌,从而减轻了肠道炎症和降低了葡萄糖水平。大鼠粪便中的短链脂肪酸水平在用黄连素或 GQD 治疗后也显著升高。此外,治疗后血清促炎细胞因子的浓度和胰腺胰岛中免疫相关基因(包括 Nfkb1、Stat1 和 Ifnrg1)的表达均显著降低。我们的研究表明,GQD 的主要作用可以归因于通过调节肠道微生物群的黄连素。所采用的策略将有助于进一步规范和广泛应用 TCM 治疗许多疾病。