Cui Huantian, Li Yuting, Wang Yuming, Jin Lulu, Yang Lu, Wang Li, Liao Jiabao, Wang Haoshuo, Peng Yanfei, Zhang Zhaiyi, Wang Hongwu, Liu Xiangguo
Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, China.
Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Front Pharmacol. 2020 Nov 27;11:584090. doi: 10.3389/fphar.2020.584090. eCollection 2020.
The dysbiosis in gut microbiota could affect host metabolism and contribute to the development of nonalcoholic fatty liver disease (NAFLD). Da-Chai-Hu decoction (DCH) has demonstrated protective effects on NAFLD, however, the exact mechanisms remain unclear. In this study, we established a NAFLD rat model using a high fat diet (HFD) and provided treatment with DCH. The changes in gut microbiota post DCH treatment were then investigated using 16S rRNA sequencing. Additionally, serum untargeted metabolomics were performed to examine the metabolic regulations of DCH on NAFLD. Our results showed that DCH treatment improved the dyslipidemia, insulin resistance (IR) and ameliorated pathological changes in NAFLD model rats. 16S rRNA sequencing and untargeted metabolomics showed significant dysfunction in gut microbiota community and serum metabolites in NAFLD model rats. DCH treatment restored the dysbiosis of gut microbiota and improved the dysfunction in serum metabolism. Correlation analysis indicated that the modulatory effects of DCH on the arachidonic acid (AA), glycine/serine/threonine, and glycerophospholipid metabolic pathways were related to alterations in the abundance of , , and in the gut microflora. In conclusion, our study revealed the ameliorative effects of DCH on NAFLD and indicated that DCH's function on NAFLD may link to the improvement of the dysbiosis of gut microbiota and the modulation of the AA, glycerophospholipid, and glycine/serine/threonine metabolic pathways.
肠道微生物群的失调会影响宿主代谢,并促进非酒精性脂肪性肝病(NAFLD)的发展。大柴胡汤(DCH)已被证明对NAFLD具有保护作用,然而,确切机制仍不清楚。在本研究中,我们使用高脂饮食(HFD)建立了NAFLD大鼠模型,并给予DCH治疗。然后使用16S rRNA测序研究DCH治疗后肠道微生物群的变化。此外,进行血清非靶向代谢组学分析以检查DCH对NAFLD的代谢调控作用。我们的结果表明,DCH治疗改善了NAFLD模型大鼠的血脂异常、胰岛素抵抗(IR),并减轻了病理变化。16S rRNA测序和非靶向代谢组学分析表明,NAFLD模型大鼠的肠道微生物群和血清代谢物存在明显功能障碍。DCH治疗恢复了肠道微生物群的失调,并改善了血清代谢功能障碍。相关性分析表明,DCH对花生四烯酸(AA)、甘氨酸/丝氨酸/苏氨酸和甘油磷脂代谢途径的调节作用与肠道微生物群中、、和丰度的改变有关。总之,我们的研究揭示了DCH对NAFLD的改善作用,并表明DCH对NAFLD的作用可能与改善肠道微生物群失调以及调节AA、甘油磷脂和甘氨酸/丝氨酸/苏氨酸代谢途径有关。