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Active Compounds Derived from Fuzheng Huayu Formula Protect Hepatic Parenchymal Cells from Apoptosis Based on Network Pharmacology and Transcriptomic Analysis.

Abstract
Fuzheng huayu formula (FZHY), an antifibrotic traditional Chinese medicine, is frequently used for the treatment of liver fibrosis. In this study, network analysis, transcriptomic analysis, assays of cell apoptosis, viability and protein expression were used for investigating the effects and mechanisms of compounds derived from FZHY on hepatic parenchymal cell (HPC) protection and hepatic stellate cell activation. Network pharmacology analysis found that 6 major compounds and 39 potential targets were important network nodes. Our analysis predicted that the active compounds of FZHY, including hederagenin, luteolin and tanshinone IIA inhibited cell apoptosis (p < 0.05), increased PI3K expression and reduced cleaved caspase 3 expression and the Bax/Bcl-w ratio (p < 0.05) in L02 cells that had apoptosis induced by TNF-α. Few significant changes caused by FZHY, hederagenin, luteolin and tanshinone IIA were observed in hepatic stellate Lx2 cells upon TGF-β1 induction. These data suggest that FZHY is active against liver fibrosis, protects hepatic parenchymal cells from apoptosis, and recovers liver function, possibly through the effects of its active compounds hederagenin, luteolin and tanshinone IIA and is involved in the inhibition of apoptosis in HPCs, possibly through regulating the PI3K, ERK, cleaved caspase 3 and Bax/Bcl-w levels.
AuthorsRong Wu, Shu Dong, Fei-Fei Cai, Xiao-Le Chen, Meng-Die Yang, Ping Liu, Shi-Bing Su
JournalMolecules (Basel, Switzerland) (Molecules) Vol. 24 Issue 2 (Jan 18 2019) ISSN: 1420-3049 [Electronic] Switzerland
PMID30669350 (Publication Type: Journal Article)
Chemical References
  • Drugs, Chinese Herbal
  • fuzheng huayu
Topics
  • Animals
  • Apoptosis (drug effects, genetics)
  • Cell Survival (drug effects)
  • Dose-Response Relationship, Drug
  • Drugs, Chinese Herbal (chemistry, pharmacokinetics, pharmacology)
  • Gene Expression Profiling
  • Gene Expression Regulation (drug effects)
  • Hepatocytes (drug effects, metabolism)
  • Male
  • Rats
  • Signal Transduction (drug effects)
  • Transcriptome

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