Sulforaphane as an inducer of glutathione prevents oxidative stress-induced cell death in a dopaminergic-like neuroblastoma cell line

J Neurochem. 2009 Dec;111(5):1161-71. doi: 10.1111/j.1471-4159.2009.06394.x. Epub 2009 Sep 22.

Abstract

The total GSH depletion observed in the substantia nigra (SN) appears to be responsible for subsequent oxidative stress (OS), mitochondrial dysfunction, and dopaminergic cell loss in patients with Parkinson's disease. A strategy to prevent the OS of dopaminergic cells in the SN may be the use of chemopreventive agents as inducers of endogenous GSH, antioxidant and phase 2 enzymes. In this study, we demonstrated that treatment of the dopaminergic-like neuroblastoma SH-SY5Y cell line with sulforaphane (SF), a cruciferous vegetables inducer, resulted in significant increases of total GSH level, NAD(P)H : quinone oxidoreductase-1, GSH-transferase and -reductase, but not GSH-peroxidase, catalase and superoxide dismutase activities. Further, the elevation of GSH levels, GSH-transferase and NAD(P)H:quinone oxidoreductase-1 activities was correlated to an increase of the resistance of SH-SY5Y cells to toxicity induced by H(2)O(2) or 6-hydroxydopamine (6-OHDA). The pre-treatment of SH-SY5Y cells with SF was also shown to prevent various apoptotic events (mitochondrial depolarization, caspase 9 and 3 activation and DNA fragmentation) and necrosis elicited by 6-OHDA. Further, the impairment of antioxidant capacity and reactive oxygen species formation at intracellular level after exposure to 6-OHDA was effectively counteracted by pre-treatment with SF. Last, both the cytoprotective and antioxidant effects of SF were abolished by the addition of buthionine sulfoximine supporting the main role of GSH in the neuroprotective effects displayed by SF. These findings show that SF may play a role in preventing Parkinson's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic Agents / pharmacology
  • Analysis of Variance
  • Anticarcinogenic Agents / pharmacology*
  • Caspase 3 / metabolism
  • Caspase 9 / metabolism
  • Cell Death / drug effects
  • Cell Line, Tumor
  • DNA Fragmentation / drug effects
  • Dopamine / metabolism*
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Enzyme-Linked Immunosorbent Assay / methods
  • Glutathione / metabolism*
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Isothiocyanates
  • Membrane Potential, Mitochondrial / drug effects
  • Membrane Potential, Mitochondrial / physiology
  • Neuroblastoma / pathology
  • Oxidative Stress / drug effects*
  • Oxidative Stress / physiology*
  • Oxidopamine / pharmacology
  • Sulfoxides
  • Thiocyanates / pharmacology*
  • Time Factors

Substances

  • Adrenergic Agents
  • Anticarcinogenic Agents
  • Isothiocyanates
  • Sulfoxides
  • Thiocyanates
  • Oxidopamine
  • Hydrogen Peroxide
  • Caspase 3
  • Caspase 9
  • sulforaphane
  • Glutathione
  • Dopamine