p-Quinone mediates 6-hydroxydopamine-induced dopaminergic neuronal death and ferrous iron accelerates the conversion of p-quinone into melanin extracellularly

J Neurosci Res. 2005 Mar 15;79(6):849-60. doi: 10.1002/jnr.20382.

Abstract

Parkinson's disease (PD) is characterized by the selective loss of dopaminergic neurons in the substantia nigra (SN). 6-Hydroxydopamine (6-OHDA), a dopaminergic neurotoxin, is detected in human brains and the urine of PD patients. Using SH-SY5Y, a human neuroblastoma cell line, we demonstrated that 6-OHDA toxicity was determined by the amount of p-quinone produced in 6-OHDA auto-oxidation rather than by reactive oxygen species (ROS). Glutathione (GSH), which conjugated with p-quinone, provided significant protection whereas catalase, which detoxified hydrogen peroxide and superoxide anions, failed to block cell death caused by 6-OHDA. Although iron accumulated in the SN of patients with PD can cause dopaminergic neuronal degeneration by enhancing oxidative stress, we found that extracellular ferrous iron promoted the formation of melanin and reduced the amount of p-quinone. The addition of ferrous iron to the culture medium inhibited caspase-3 activation and apoptotic nuclear morphologic changes and blocked 6-OHDA-induced cytotoxicity in SH-SY5Y cells and primary cultured mesencephalic dopaminergic neurons. These data suggested that generation of p-quinone played a pivotal role in 6-OHDA-induced toxicity and extracellular iron in contrast to intracellular iron was protective rather than harmful because it accelerated the conversion of p-quinone into melanin.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Antioxidants / pharmacology
  • Benzoquinones / pharmacology*
  • Bisbenzimidazole
  • Caspase 3
  • Caspases / metabolism
  • Cell Death / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Chromatography, High Pressure Liquid / methods
  • Dopamine / metabolism*
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Electrochemistry / methods
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Immunohistochemistry / methods
  • Iron / pharmacology*
  • L-Lactate Dehydrogenase / metabolism
  • Melanins / metabolism*
  • Mesencephalon / cytology
  • Models, Biological
  • Neuroblastoma
  • Neurons / drug effects*
  • Neurons / metabolism*
  • Oxidopamine / pharmacology
  • Rats
  • Reactive Oxygen Species
  • Tetrazolium Salts
  • Thiazoles
  • Time Factors
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Antioxidants
  • Benzoquinones
  • Melanins
  • Reactive Oxygen Species
  • Tetrazolium Salts
  • Thiazoles
  • quinone
  • Oxidopamine
  • Hydrogen Peroxide
  • Iron
  • L-Lactate Dehydrogenase
  • Tyrosine 3-Monooxygenase
  • CASP3 protein, human
  • Casp3 protein, rat
  • Caspase 3
  • Caspases
  • thiazolyl blue
  • Bisbenzimidazole
  • Dopamine