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

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

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.

Keywords: Gegen Qinlian Decoction; Hepatic lipid metabolism; Inflammation; Non-alcoholic steatohepatitis; Oxidative stress.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Antioxidants / pharmacology*
  • Biomarkers
  • Cell Line
  • Cytokines / metabolism
  • Disease Models, Animal
  • Drugs, Chinese Herbal / pharmacology*
  • Female
  • Gene Expression Profiling
  • Inflammation Mediators / metabolism
  • Lipid Metabolism / drug effects
  • Lipopolysaccharides / immunology
  • Mice
  • Models, Biological
  • Non-alcoholic Fatty Liver Disease / drug therapy
  • Non-alcoholic Fatty Liver Disease / etiology*
  • Non-alcoholic Fatty Liver Disease / metabolism*
  • Non-alcoholic Fatty Liver Disease / pathology
  • Oxidative Stress / drug effects
  • Proteomics / methods
  • Rats
  • Signal Transduction / drug effects*
  • Toll-Like Receptor 4 / metabolism*
  • Transcriptome

Substances

  • Anti-Inflammatory Agents
  • Antioxidants
  • Biomarkers
  • Cytokines
  • Drugs, Chinese Herbal
  • Inflammation Mediators
  • Lipopolysaccharides
  • Toll-Like Receptor 4
  • gegenqinlian