Akt/Nrf2 activated upregulation of heme oxygenase-1 involves in the role of Rg1 against ferrous iron-induced neurotoxicity in SK-N-SH cells

Neurotox Res. 2013 Jul;24(1):71-9. doi: 10.1007/s12640-012-9362-3. Epub 2012 Nov 27.

Abstract

Iron accumulation is considered to be involved in the pathogenesis of Parkinson's disease (PD). Our previous studies have observed that Rg1, a major pharmacologically active ingredient from Ginseng, could protect dopaminergic neurons by reducing nigral iron levels through regulating the expression of iron transporters in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced PD mice. The aim of this study is to investigate other mechanism involved in the cytoprotection of Rg1 against iron-induced neurotoxicity in human neuroblastoma SK-N-SH cells. Significant rescue of Rg1 on cell viability against 100 μM ferrous iron-induced neurotoxicity was observed. Upregulation of heme oxygenase-1 (HO-1) and Cu-Zn superoxide dismutase (Cu/Zn SOD) were observed in Rg1 pretreated group. Moreover, Rg1 pretreatment induces Nrf2 nuclear translocation, which is upstream of HO-1 expression, and activated PI3K/Akt pathway was also observed in Rg1 pretreated group. This could antagonize iron-induced increase in intracellular reactive oxygen species and decrease in mitochondrial transmembrane potential. These results suggest that the neuroprotective effects of Rg1 against iron toxicity are attributed to the anti-oxidative properties by activating Akt/Nrf2 pathway and increasing Nrf2-induced expression of HO-1 and Cu/Zn SOD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cell Survival / drug effects
  • Down-Regulation
  • Ferrous Compounds / antagonists & inhibitors*
  • Ferrous Compounds / toxicity
  • Ginsenosides / pharmacology*
  • Heme Oxygenase-1 / metabolism*
  • Humans
  • Iron / toxicity*
  • Membrane Potential, Mitochondrial / drug effects
  • NF-E2-Related Factor 2 / metabolism*
  • Neuroprotective Agents / pharmacology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Reactive Oxygen Species / metabolism
  • Superoxide Dismutase / metabolism
  • Up-Regulation

Substances

  • Ferrous Compounds
  • Ginsenosides
  • NF-E2-Related Factor 2
  • Neuroprotective Agents
  • Reactive Oxygen Species
  • ferrous sulfate
  • Iron
  • Heme Oxygenase-1
  • Superoxide Dismutase
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt