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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Gegen Qinlian Decoction abates nonalcoholic steatohepatitis associated liver injuries via anti-oxidative stress and anti-inflammatory response involved inhibition of toll-like receptor 4 signaling pathways
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Gegen Qinlian Decoction abates nonalcoholic steatohepatitis associated liver injuries via anti-oxidative stress and anti-inflammatory response involved inhibition of toll-like receptor 4 signaling pathways

机译:GEGEN Qinlian汤通过抗氧化应激和抗炎反应抑制非酒精性脂肪磷脂炎相关肝损伤,包括抑制Toll样受体4信号通路

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摘要

Gegen Qilian Decoction (GGQLD) is a well-established classic Chinese medicine prescription in treating nonalcoholic steatohepatitis (NASH). However, the molecular mechanism of GGQLD action on NASH is still not clear. This study aimed to assess the anti-NASH effect of GGQLD, and to explore its molecular mechanisms in vivo and in vitro. In HFD-fed rats, GGQLD decreased significantly serum triglyceride (TG), cholesterol (CHO), total bile acid (TBA), low-density lipoprotein (LDL), free fatty acid (FFA) and lipopolysaccharide (LPS) levels, increased levels of differentially expressed proteins (DEPs) Ahcy, Gpx1, Mat1a, GNMT, and reduced the expression of ALDOB. In RAW264.7 macrophages, GGQLD reduced the expression levels of inflammatory factors TNF-alpha and IL-6 mRNA, and diminished NASH by increasing differentially expressed genes (DEGs) CBS, Mat1a, Hnf4a and Ppara to reduce oxidative stress or lipid metabolism. The results of DEGs verification also showed that GGQLD up-regulated expressions of Hnf4a, Ppara and Cbs genes. In HepG2 cells, GGQLD decreased IL-6 levels and intracellular TG content, and inhibited FFA-induced expression of toll-like receptor 4 (TLR4). In summary, GGQLD abates NASH associated liver injuries via anti-oxidative stress and anti-inflammatory response involved inhibition of TLR4 signal pathways. These findings provide new insights into the anti-NASH therapy by GGQLD.
机译:Gegen Qilian汤(GGQLD)是一种成熟的经典中医处方治疗非酒精性脂肪肝炎(纳什)。然而,GGQLD动作对纳什的分子机制仍未清楚。本研究旨在评估GGQLD的抗尿效应,探讨其体内和体外分子机制。在HFD喂养大鼠中,GGQLD显着降低血清甘油三酯(TG),胆固醇(CHO),总胆汁酸(TBA),低密度脂蛋白(LDL),游离脂肪酸(FFA)和脂多糖(LPS)水平,增加差异表达的蛋白质(DEPS)Ahcy,GPX1,Mat1a,Gnmt和降低了Aldob的表达。在Raw264.7巨噬细胞中,GGQLD降低了炎症因子TNF-α和IL-6 mRNA的表达水平,通过增加差异表达基因(DEGS)CBS,MAT1A,HNF4A和PPARA来减少肿瘤以减少氧化应激或脂质代谢。 Degs验证的结果还表明,GGQLD上调的HNF4A,PPARA和CBS基因的表达。在HepG2细胞中,GGQLD降低IL-6水平和细胞内Tg含量,抑制FFA诱导的Toll样受体4的表达(TLR4)。总之,GGQLD通过抗氧化应激和抗炎反应抑制TLR4信号途径的抑制作用。这些调查结果为GGQLD提供了新的抗养牛治疗的洞察。

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