首页> 美国卫生研究院文献>Frontiers in Pharmacology >Geniposide and Chlorogenic Acid Combination Ameliorates Non-alcoholic Steatohepatitis Involving the Protection on the Gut Barrier Function in Mouse Induced by High-Fat Diet
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Geniposide and Chlorogenic Acid Combination Ameliorates Non-alcoholic Steatohepatitis Involving the Protection on the Gut Barrier Function in Mouse Induced by High-Fat Diet

机译:ip子苷和绿原酸的组合改善了非酒精性脂肪性肝炎,涉及高脂饮食诱导的小鼠肠道屏障功能的保护

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摘要

Gut-liver axis is increasingly recognized to be involved in the pathogenesis and progression of non-alcoholic fatty liver disease (NAFLD). The gut microbiota and intestinal permeability have been demonstrated to be the key players in the gut-liver cross talk in NAFLD. Geniposide and chlorogenic acid (GC) combination is derived from a traditional Chinese medicine, Qushi Huayu Decoction (QHD), which has been used in clinic for NAFLD treatment for decades in China and validated in multiple animal models of NAFLD. GC combination previously has been demonstrated to treat NAFLD via modulation on the gut microbiota composition. In the present study, the effects of GC combination on gut barrier function in NAFLD were evaluated, and QHD and sodium butyrate (NaB), the intestinal mucosa protectant, were used as positive control. The therapeutic effect of GC combination on NAFLD were confirmed by amelioration on non-alcoholic steatohepatitis (NASH) induced by high-fat diet (HFD) in mouse, which was comparable to that of QHD. Simultaneously, GC combination was found to reduce the signaling of gut-derived lipopolysaccharide (LPS) including hepatic LPS binding protein, Toll like receptor 4, interleukin-1β, tumor necrosis factor –α, and Kupffer cells infiltration. Furthermore, GC combination reduced LPS and D-lactate in plasma, restoring the colonic tight junction (TJ) expression and inhibited colonic TJs disassembly by down-regulation on RhoA/ROCK signaling in NASH induced by HFD. On the other hand, NASH was also alleviated in NaB group. The results of the present study suggested the important role of protection on gut barrier function in NAFLD treatment, which contributed to the therapeutic effects of GC combination on NASH.
机译:越来越多的肠肝轴参与了非酒精性脂肪肝疾病(NAFLD)的发病机理和进展。肠道菌群和肠道通透性已被证明是NAFLD肠道-肝脏相声的关键因素。 ip子苷和绿原酸(GC)的组合源自中药曲氏化瘀汤(QHD),该药已在中国用于NAFLD治疗数十年,并在多种NAFLD动物模型中得到验证。先前已证明GC组合可通过调节肠道菌群组成来治疗NAFLD。在本研究中,评估了GC组合对NAFLD肠屏障功能的影响,并将QHD和肠黏膜保护剂丁酸钠(NaB)用作阳性对照。通过改善高脂饮食(HFD)引起的小鼠非酒精性脂肪性肝炎(NASH),证实了GC组合对NAFLD的治疗效果,与QHD相当。同时,发现GC组合可减少肠源性脂多糖(LPS)的信号传导,包括肝LPS结合蛋白,Toll样受体4,白介素-1β,肿瘤坏死因子-α和Kupffer细胞浸润。此外,GC组合通过下调HFD诱导的NASH中RhoA / ROCK信号传导,降低血浆中LPS和D-乳酸,恢复结肠紧密连接(TJ)表达,并抑制结肠TJs拆卸。另一方面,NaB组也减轻了NASH。本研究结果表明,在NAFLD治疗中保护肠屏障功能具有重要作用,这有助于GC联合治疗对NASH的治疗作用。

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