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首页> 外文期刊>World Journal of Gastroenterology >Fecal microbiota transplantation prevents hepatic encephalopathy in rats with carbon tetrachloride-induced acute hepatic dysfunction
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Fecal microbiota transplantation prevents hepatic encephalopathy in rats with carbon tetrachloride-induced acute hepatic dysfunction

机译:粪便菌群移植预防四氯化碳诱导的急性肝功能不全大鼠肝性脑病

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AIM To investigate whether fecal microbiota transplantation (FMT) prevents hepatic encephalopathy (HE) in rats with carbon tetrachloride (CCl4)-induced acute hepatic dysfunction. METHODS A rat model of HE was established with CCl4. Rat behaviors and spatial learning capability were observed, and hepatic necrosis, intestinal mucosal barrier, serum ammonia levels and intestinal permeability were determined in HE rats receiving FMT treatment. Furthermore, the expression of tight junction proteins (Claudin-1, Claudin-6 and Occludin), Toll-like receptor (TLR) 4/TLR9, interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α was examined. RESULTS FMT improved rat behaviors, HE grade and spatial learning capability. Moreover, FMT prevented hepatic necrosis and intestinal mucosal barrier damage, leading to hepatic clearance of serum ammonia levels and reduced intestinal permeability. The expression of TLR4 and TLR9, two potent mediators of inflammatory response, was significantly downregulated in the liver of rats treated with FMT. Consistently, circulating pro-inflammatory factors such as interleukin (IL)-1β, IL-6 and tumor necrosis factor-α were remarkably decreased, indicating that FMT is able to limit systemic inflammation by decreasing the expression of TLR4 and TLR9. Importantly, HE-induced loss of tight junction proteins (Claudin-1, Claudin-6 and Occludin) was restored in intestinal tissues of rats receiving FMT treatment. CONCLUSION FMT enables protective effects in HE rats, and it improves the cognitive function and reduces the liver function indexes. FMT may cure HE by altering the intestinal permeability and improving the TLR response of the liver.
机译:目的探讨粪便微生物菌群移植(FMT)是否能预防四氯化碳(CCl 4 )诱发的急性肝功能不全大鼠的肝性脑病(HE)。方法用CCl 4 建立大鼠HE模型。观察大鼠行为和空间学习能力,并测定接受FMT治疗的HE大鼠肝坏死,肠粘膜屏障,血清氨水平和肠通透性。此外,紧密连接蛋白(Claudin-1,Claudin-6和Occludin),Toll样受体(TLR)4 / TLR9,白介素(IL)-1β,IL-6和肿瘤坏死因子(TNF)-α的表达被检查了。结果FMT改善了大鼠的行为,HE等级和空间学习能力。此外,FMT预防了肝坏死和肠粘膜屏障破坏,从而导致肝清除血清氨水平并降低了肠通透性。在FMT处理的大鼠肝脏中,TLR4和TLR9是炎症反应的两个有效介体,其表达明显下调。一致地,循环促炎因子如白介素(IL)-1β,IL-6和肿瘤坏死因子-α显着降低,表明FMT能够通过降低TLR4和TLR9的表达来限制全身性炎症。重要的是,在接受FMT治疗的大鼠的肠组织中,HE诱导的紧密连接蛋白(Claudin-1,Claudin-6和Occludin)的丢失得以恢复。结论FMT对HE大鼠具有保护作用,可改善认知功能,降低肝功能指标。 FMT可以通过改变肠的通透性和改善肝脏的TLR反应来治愈HE。

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