Pan Tong, Zheng Shujun, Zheng Weiwei, Shi Chao, Ning Ke, Zhang Qinghui, Xie Yanbo, Xiang Hongyu, Xie Qiuhong
National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University, Changchun, China.
School of Life Sciences, Jilin University, Changchun, China.
Front Microbiol. 2022 Oct 12;13:1022403. doi: 10.3389/fmicb.2022.1022403. eCollection 2022.
There is a lot of evidence that oral hypoglycemic drugs work by affecting gut microbes, but the key strains responsible for this effect are not well known. Huang-Qi-Ling-Hua-San (HQLHS), composed of , , , and L., is a specially designed Chinese medicine formula to treat type 2 diabetes (T2D). In this study, a mouse model of T2D induced by high-fat diet and streptozotocin was used to explore the mechanism of HQLHS in improving hyperglycemia and hyperlipidemia through multiple rounds of animal experiments, such as HQLHS feeding, fecal microbiota transplantation (FMT), and live bacteria feeding, so as to explore the potential target intestinal flora in its hypoglycemic effect. Results show that such specific taxa as , , , , and were identified to be preferably enriched by HQLHS and then assumed to be the target microbes. Herein, FMT was used to test if the upregulated beneficial bacteria by HQLHS play a therapeutic role. The strain DSM 22607 and the strain DSM 102800 were selected to test the beneficial effect of taxa on T2D. Diabetic animals supplemented with these strains showed the improvement in blood glucose and lipid metabolism, the promotion of GLP-1 secretion, the increase in antioxidant capacity, the inhibition of hepatic gluconeogenesis, the suppression of intestinal glucose absorption, the enhancement of intestinal barrier, reduced LPS-induced inflammation, and the reduction of branched amino acids (BCAAs) content in the liver. Overall, these data demonstrate that plays a beneficial role in T2D and is a target for the action of HQLHS therapy.
有大量证据表明口服降糖药通过影响肠道微生物起作用,但导致这种作用的关键菌株尚不清楚。黄芪苓花散(HQLHS)由[具体成分未给出]组成,是一种专门设计用于治疗2型糖尿病(T2D)的中药配方。在本研究中,通过高脂饮食和链脲佐菌素诱导的T2D小鼠模型,经过多轮动物实验,如HQLHS喂养、粪便微生物群移植(FMT)和活菌喂养,来探索HQLHS改善高血糖和高血脂的机制,以探究其降糖作用中潜在的目标肠道菌群。结果表明,[具体菌属未给出]等特定分类群被确定为HQLHS优先富集的菌属,进而被假定为目标微生物。在此,使用FMT来测试HQLHS上调的有益细菌是否发挥治疗作用。选择菌株DSM 22607和菌株DSM 102800来测试[具体菌属]分类群对T2D的有益作用。补充这些菌株的糖尿病动物在血糖和脂质代谢方面有所改善,促进了胰高血糖素样肽-1(GLP-1)的分泌,抗氧化能力增强,抑制了肝糖异生,抑制了肠道葡萄糖吸收,增强了肠道屏障,减少了脂多糖诱导的炎症,并降低了肝脏中支链氨基酸(BCAAs)的含量。总体而言,这些数据表明[具体菌属]在T2D中发挥有益作用,是HQLHS治疗作用的靶点。