Role of reactive oxygen species in extracellular signal-regulated protein kinase phosphorylation and 6-hydroxydopamine cytotoxicity

J Biosci. 2003 Feb;28(1):83-9. doi: 10.1007/BF02970136.

Abstract

A number of reports indicate the potential for redox signalling via extracellular signal-regulated protein kinases (ERK) during neuronal injury. We have previously found that sustained ERK activation contributes to toxicity elicited by 6-hydroxydopamine (6-OHDA) in the B65 neuronal cell line. To determine whether reactive oxygen species (ROS) play a role in mediating ERK activation and 6-OHDA toxicity, we examined the effects of catalase, superoxide dismutase (SOD1), and metalloporphyrin antioxidants ('SOD mimetics') on 6-OHDA-treated cells. We found that catalase and metalloporphyrin antioxidants not only conferred protection against 6-OHDA but also inhibited development of sustained ERK phosphorylation in both differentiated and undifferentiated B65 cells. However, exogenously added SOD1 and heat-inactivated catalase had no effect on either toxicity or sustained ERK phosphorylation. This correlation between antioxidant protection and inhibition of 6-OHDA-induced sustained ERK phosphorylation suggests that redox regulation of ERK signalling cascades may contribute to neuronal toxicity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Antioxidants / pharmacology
  • Catalase / metabolism
  • Catalase / pharmacology
  • Cell Differentiation / drug effects
  • Cell Line, Tumor
  • Enzyme Activation
  • Metalloporphyrins / metabolism
  • Metalloporphyrins / pharmacology
  • Mitogen-Activated Protein Kinases / metabolism*
  • Neurons / drug effects*
  • Oxidopamine / toxicity*
  • Phosphorylation
  • Rats
  • Reactive Oxygen Species / metabolism*
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase / pharmacology

Substances

  • Antioxidants
  • Metalloporphyrins
  • Reactive Oxygen Species
  • Oxidopamine
  • Catalase
  • Superoxide Dismutase
  • Mitogen-Activated Protein Kinases