Induced expression of early response genes/oxidative injury in rat pheochromocytoma (PC12) cell line by 6-hydroxydopamine: implication for Parkinson's disease

Neurosci Lett. 2002 Sep 13;330(1):89-93. doi: 10.1016/s0304-3940(02)00714-0.

Abstract

The expression of early response gene proteins c-Fos, c-Jun, and GAP-43 and their association with 6-hydroxydopamine (6-OHDA)-mediated oxidative injury were investigated using catecholaminergic PC12 cell line. Significant induction in the expression of c-Fos (P < 0.01), c-Jun (P < 0.001) and GAP-43 (P < 0.05) was observed following 2 h exposure to 6-OHDA (10(-6) M), which persisted during 24 h of observation. The exposed cells exhibited an increase in lipid peroxidation (48, 59 and 33%) along with decreased catalase activity (49, 30 and 13%) and glutathione levels (39, 28 and 16%) following 24, 48 and 72 h exposure, respectively. A concentration-dependent functional impairment of mitochondria as studied by 3-(4,5-dimethyl thiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay and decreased cell survival were also observed following 6-OHDA (10(-4), 10(-5) M) exposure for 24, 48 and 72 h. The results indicate a role of the early response gene in oxidative stress-mediated dopaminergic cell death by 6-OHDA. Similar mechanisms may also be operative in the development of Parkinson's disease, as an increased presence/formation of endogenous 6-OHDA has been reported in Parkinson's patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • GAP-43 Protein / biosynthesis
  • GAP-43 Protein / genetics*
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Genes, fos / drug effects*
  • Genes, jun / drug effects*
  • Oxidative Stress / drug effects
  • Oxidative Stress / genetics*
  • Oxidopamine / metabolism
  • Oxidopamine / toxicity*
  • PC12 Cells
  • Parkinson Disease / genetics*
  • Parkinson Disease / metabolism*
  • Rats

Substances

  • GAP-43 Protein
  • Oxidopamine