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葛根芩连汤通过抑制 toll 样受体 4 信号通路的抗炎和抗氧化应激反应减轻非酒精性脂肪性肝炎相关肝损伤。

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.

机构信息

College of Pharmacy, Jiangxi University of Traditional Chinese Medicine, Nanchang, Jiangxi, 330004, PR China.

College of Life Science, Nanchang University, Nanchang, 330031, PR China.

出版信息

Biomed Pharmacother. 2020 Jun;126:110076. doi: 10.1016/j.biopha.2020.110076. Epub 2020 Mar 10.

DOI:10.1016/j.biopha.2020.110076
PMID:32169759
Abstract

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-α and IL-6 mRNA, and diminished NASH by increasing differentially expressed genes (DEGs) CBS, Mat1a, Hnf4α and Pparα to reduce oxidative stress or lipid metabolism. The results of DEGs verification also showed that GGQLD up-regulated expressions of Hnf4α, Pparα 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.

摘要

肝积清对非酒精性脂肪性肝炎的作用及机制研究

肝积清(GGQLD)是治疗非酒精性脂肪性肝炎(NASH)的经典中药方剂。然而,其作用于 NASH 的分子机制尚不清楚。本研究旨在评估 GGQLD 对 NASH 的防治作用,并从体内和体外水平探讨其作用机制。在高脂饮食喂养大鼠中,GGQLD 能显著降低血清三酰甘油(TG)、胆固醇(CHO)、总胆汁酸(TBA)、低密度脂蛋白(LDL)、游离脂肪酸(FFA)和内毒素(LPS)水平,上调 Ahcy、Gpx1、Mat1a、GNMT 等差异表达蛋白(DEPs)的表达,下调 ALDOB 的表达。在 RAW264.7 巨噬细胞中,GGQLD 可降低促炎因子 TNF-α和 IL-6mRNA 的表达水平,通过上调 CBS、Mat1a、Hnf4α和 Pparα 等差异表达基因(DEGs),减少氧化应激或脂质代谢,减轻 NASH 症状。DEGs 验证结果也表明,GGQLD 可上调 Hnf4α、Pparα和 Cbs 等基因的表达。在 HepG2 细胞中,GGQLD 可降低 IL-6 水平和细胞内 TG 含量,抑制 FFA 诱导的 TLR4 表达。综上,GGQLD 可能通过抑制 TLR4 信号通路,发挥抗炎抗氧化作用,减轻 NASH 相关肝损伤。这些发现为 GGQLD 防治 NASH 提供了新的思路。

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