Protection of epidermal growth factor against clivorine-induced mitochondrial-mediated apoptosis in hepatocytes

Environ Toxicol. 2010 Jun;25(3):304-9. doi: 10.1002/tox.20500.

Abstract

Pyrrolizidine alkaloids (PAs) are well-known natural hepatotoxins. In this study, we investigated the protection of epidermal growth factor (EGF) against the hepatotoxicity of clivorine, which is an otonecine-type PA from traditional Chinese medicine Ligularia hodgsonii Hook. Cell viability assay and cell morphology observation showed that EGF (1 ng/mL) reversed clivorine-induced cytotoxicity on human normal liver L-02 cells. EGF (1 ng/mL) also inhibited clivorine-induced DNA fragmentation and caspase-3 cleavage. Our previous study has showed that antiapoptotic Bcl-xL degradation and mitochondrial-mediated apoptosis was involved in clivorine-induced hepatotoxicity. In this study, we found that EGF (1 ng/mL) inhibited clivorine-induced antiapoptotic Bcl-xL protein decrease, caspase-9 activation, and release of cytosolic cytochrome C. We further investigated the effects of vascular epidermal growth factor, basic fibroblast growth factor, and insulin-like growth factor-1 on clivorine-induced cytotoxicity, and there is no significant protection observed. Our results suggest that EGF exerts its protective effects against clivorine-induced hepatotoxicity probably by modulating mitochondrial-mediated apoptotic signal pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Blotting, Western
  • Caspase 3 / metabolism
  • Caspase 9 / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Cytochromes c / metabolism
  • DNA Fragmentation / drug effects
  • Electrophoresis, Polyacrylamide Gel
  • Epidermal Growth Factor / pharmacology*
  • Hepatocytes / drug effects*
  • Hepatocytes / pathology
  • Humans
  • Mitochondria, Liver / drug effects*
  • Mitochondria, Liver / pathology
  • Protective Agents / pharmacology*
  • Pyrrolizidine Alkaloids / toxicity*
  • bcl-X Protein / metabolism

Substances

  • BCL2L1 protein, human
  • Protective Agents
  • Pyrrolizidine Alkaloids
  • bcl-X Protein
  • Epidermal Growth Factor
  • Cytochromes c
  • Caspase 3
  • Caspase 9
  • clivorine