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Modulation of the Gut Microbiota in Rats by Hugan Qingzhi Tablets during the Treatment of High-Fat-Diet-Induced Nonalcoholic Fatty Liver Disease

机译:高脂饮食诱发非酒精性脂肪肝病治疗高脂饮食脂肪肝疾病中Hugan Qingzhi片剂的肠道微生物肿瘤

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摘要

Background. Accumulative evidence showed that gut microbiota was important in regulating the development of nonalcoholic fatty liver disease (NAFLD). Hugan Qingzhi tablet (HQT), a lipid-lowering and anti-inflammatory medicinal formula, has been used to prevent and treat NAFLD. However, its mechanism of action is unknown. The aim of this study was to confirm whether HQT reversed the gut microbiota dysbiosis in NAFLD rats. Methods. We established an NAFLD model of rats fed with a high-fat diet (HFD), which was given different interventions, and measured the level of liver biochemical indices and inflammatory factors. Liver tissues were stained with hematoxylin-eosin and oil red O. Changes in the gut microbiota composition were analyzed using 16S rRNA sequencing. Results. The hepatic histology and biochemical data displayed that HQT exhibited protective effects on HFD-induced rats. Moreover, HQT also reduced the abundance of the Firmicutes/Bacteroidetes ratio in HFD-fed rats and modified the gut microbial species at the genus level, increasing the abundances of gut microbiota which were reported to have an effect on relieving NAFLD, such as Ruminococcaceae, Bacteroidales_S24-7_group, Bifidobacteria, Alistipes, and Anaeroplasma, and significantly inhibiting the relative abundance of Enterobacteriaceae, Streptococcus, Holdemanella, Allobaculum, and Blautia, which were reported to be potentially related to NAFLD. Spearman’s correlation analysis found that [Ruminococcus]_gauvreauii_group, Lachnoclostridium, Blautia, Allobaculum, and Holdemanella exhibited significant (p<0.001) positive correlations with triglyceride, cholesterol, low-density lipoprotein cholesterol, interleukin-6, interleukin-1β, tumor necrosis factor-α, and body weight and negative correlations with high-density lipoprotein cholesterol (p<0.001). The norank_f__Bacteroidales_S24-7_group and Alistipes showed an opposite trend. Moreover, the HQT could promote flavonoid biosynthesis compared with the HFD group. Conclusion. In summary, the HQT has potential applications in the prevention and treatment of NAFLD, which may be closely related to its modulatory effect on the gut microbiota.
机译:背景。累积的证据表明,肠道菌群是调控非酒精性脂肪性肝病(NAFLD)的发展具有重要意义。护肝清脂片(HQT),降脂和抗炎药物配方,已被用于预防和治疗NAFLD。然而,其作用机制尚不清楚。这项研究的目的是确认是否HQT逆转NAFLD大鼠肠道菌群生态失调。方法。我们建立了与高脂肪食物(HFD),其给定的不同的干预喂养大鼠的NAFLD模型,并测量肝生化指标和炎性因子的水平。肝组织用苏木精 - 曙红和油红染色使用的16S rRNA测序O.变化肠道微生物组合物进行了分析。结果。肝组织学和生物化学数据显示的显示HQT上HFD诱导的大鼠的保护作用。此外,HQT也减少了厚壁菌门/拟杆菌比率在HFD喂养大鼠和改性在属水平肠道微生物物种,增加其据报道具有在缓解NAFLD,如Ruminococcaceae的效果肠道菌群的丰度的丰度, Bacteroidales_S24-7_group,双歧杆菌,Alistipes,和Anaeroplasma,和显著抑制肠杆菌科细菌,链球菌属,Holdemanella,Allobaculum和Blautia,将其报告给潜在地相关的NAFLD的相对丰度。 Spearman相关分析发现,[瘤胃球菌] _gauvreauii_group,Lachnoclostridium,Blautia,Allobaculum和Holdemanella表现出显著(P <0.001)与甘油三酯,胆固醇,低密度脂蛋白胆固醇的正相关关系,白介素-6,白介素1β,肿瘤坏死因子α,和体重,并与高密度脂蛋白胆固醇(p <0.001)负相关。的norank_f__Bacteroidales_S24-7_group和Alistipes显示出相反的趋势。此外,HQT可以与HFD组相比,促进类黄酮的生物合成。结论。综上所述,HQT在NAFLD的预防和治疗,这可能是密切相关的对肠道菌群的调节作用潜在的应用。

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