Development of a novel anti-liver fibrosis formula with luteolin, licochalcone A, aloe-emodin and acacetin by network pharmacology and transcriptomics analysis

Pharm Biol. 2021 Dec;59(1):1594-1606. doi: 10.1080/13880209.2021.1999275.

Abstract

Context: Xiaoyaosan decoction (XYS), a classical Traditional Chinese Medicine (TCM) formula is used to treat liver fibrosis in clinics.

Objective: This study explores defined compound combinations from XYS decoction to treat liver fibrosis.

Materials and methods: Network pharmacology combined with transcriptomics analysis was used to analyze the XYS decoction and liver depression and spleen deficiency syndrome liver fibrosis. From the constructed XYS-Syndrome-liver fibrosis network, the top 10 active formulas were developed by topological analysis according to network stability. The most active formula was determined by in vitro study. The anti-fibrosis effect was evaluated by in vitro and in vivo studies.

Results: According to the network XYS-Syndrome-liver fibrosis network, 8 key compounds and 255 combinations were predicted from in XYS. Luteolin, licochalcone A, aloe-emodin and acacetin formula (LLAAF) had a synergistic effect on the proliferation inhibition of hepatic stellate cells compared to individual compounds alone. The treatment of XYS and LLAAF showed a similar anti-liver fibrotic effect that reduced histopathological changes of liver fibrosis, Hyp content and levels of α-SMA and collagen I in CCl4-induced liver fibrosis in rats. Transcriptomics analysis revealed LLAAF regulated PI3K-Akt, AMPK, FoxO, Jak-STAT3, P53, cell cycle, focal adhesion, and PPAR signalling. Furthermore, LLAAF was confirmed to regulate Jak-STAT and PI3K-Akt-FoxO signalling in vitro and in vivo.

Conclusions: This study developed a novel anti-liver formula LLAAF from XYS, and demonstrated its anti-liver fibrotic activity which may be involved in the regulation of Jak-STAT and PI3K-Akt-FoxO signalling.

Keywords: LLAAF; Xiaoyaosan decoction; anti-liver fibrotic effect.

MeSH terms

  • Animals
  • Anthraquinones / administration & dosage
  • Anthraquinones / pharmacology
  • Cell Line
  • Chalcones / administration & dosage
  • Chalcones / pharmacology
  • Drug Synergism
  • Drugs, Chinese Herbal / administration & dosage
  • Drugs, Chinese Herbal / chemistry
  • Drugs, Chinese Herbal / pharmacology*
  • Flavones / administration & dosage
  • Flavones / pharmacology
  • Hepatic Stellate Cells / drug effects*
  • Hepatic Stellate Cells / pathology
  • Humans
  • Liver Cirrhosis / drug therapy*
  • Luteolin / administration & dosage
  • Luteolin / pharmacology
  • Male
  • Network Pharmacology
  • Rats
  • Rats, Wistar
  • Signal Transduction / drug effects
  • Transcriptome

Substances

  • Anthraquinones
  • Chalcones
  • Drugs, Chinese Herbal
  • Flavones
  • xiaoyaosan
  • aloe emodin
  • licochalcone A
  • Luteolin
  • acacetin

Grants and funding

This work was supported by grants from the Major Project of Shanghai Municipal S&T Commission [19401972300] and National Science Foundation of China [81330084].