Geniposide activates GSH S-transferase by the induction of GST M1 and GST M2 subunits involving the transcription and phosphorylation of MEK-1 signaling in rat hepatocytes

Toxicol Appl Pharmacol. 2005 Oct 15;208(2):155-62. doi: 10.1016/j.taap.2005.02.013.

Abstract

Geniposide, an iridoid glycoside isolated from the fruit of Gardenia jasminoides Ellis, has biological capabilities of detoxication, antioxidation, and anticarcinogenesis. We have recently found that geniposide possesses a potential for detoxication by inducing GST activity and the expression of GST M1 and GST M2 subunits. In this study, the signaling pathway of geniposide leading to the activation of GSH S-transferase (GST) was investigated. Primary cultured rat hepatocytes were treated with geniposide in the presence or absence of mitogen-activated protein kinase (MAPK) inhibitors and examined for GST activity, expression of GST M1 and M2 subunits, and protein levels of MAPK signaling proteins. Western blotting data demonstrated that geniposide induced increased protein levels of GST M1 and GST M2 (approximately 1.76- and 1.50-fold of control, respectively). The effect of geniposide on the increased protein levels of GST M1 and GST M2 was inhibited by the MEK-1 inhibitor PD98059, but not by other MAPK inhibitors. The GST M1 and GST M2 transcripts as determined by RT-PCR and GST activity were also inhibited concurrently by the MEK-1 inhibitor PD98059. The protein levels of up- and down-stream effectors of the MEK-1, including Ras, Raf, and Erk1/2, and the phosphorylation state of Erk1/2 were found to be induced by geniposide, indicating a two-phase influence of geniposide. The results suggest that geniposide induced GST activity and the expression of GST M1 and GST M2 acting through MEK-1 pathway by activating and increasing expression of Ras/Raf/MEK-1 signaling mediators.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Glutathione Transferase / biosynthesis*
  • Glutathione Transferase / genetics
  • Hepatocytes / drug effects
  • Hepatocytes / enzymology*
  • Iridoids / pharmacology*
  • Isoenzymes / biosynthesis
  • Isoenzymes / genetics
  • MAP Kinase Kinase 1 / genetics*
  • MAP Kinase Kinase 1 / physiology*
  • Male
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Phosphorylation
  • Pyrans / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects
  • Transcription, Genetic

Substances

  • Enzyme Inhibitors
  • Iridoids
  • Isoenzymes
  • Pyrans
  • geniposide
  • Glutathione Transferase
  • glutathione S-transferase M1
  • glutathione S-transferase Mu 2
  • Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 1