Role of oxidative damage in Friedreich's ataxia

Neurochem Res. 2004 Mar;29(3):561-7. doi: 10.1023/b:nere.0000014826.00881.c3.


Plasma malondialdehyde (MDA) levels were raised in Friedreich's ataxia (FRDA) patients. These levels correlated with increasing age and disease duration, suggesting lipid peroxidation increased with disease progression. Using fibroblasts from FRDA patients we observed that GSH levels and aconitase activities were normal, suggesting their antioxidant status was unchanged. When exposed to various agents to increase free radical generation we observed that intracellular superoxide generation induced by paraquat caused enhanced oxidative damage. This correlated with the size of the GAA1 expansion, suggesting decreased frataxin levels may render the cells more vulnerable to mild oxidative stress. More severe oxidative stress induced by hydrogen peroxide caused increased cell death in FRDA fibroblasts but was not significantly different from control cells. We propose that abnormal respiratory chain function and iron accumulation may lead to a progressive increase in oxidative damage, but increased sensitivity to free radicals may not require detectable respiratory chain dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aconitate Hydratase / metabolism
  • Adolescent
  • Adult
  • Age of Onset
  • Biomarkers / blood
  • Cell Survival / drug effects
  • Child
  • Chlorides
  • Ferric Compounds / pharmacology
  • Fibroblasts / drug effects
  • Fibroblasts / enzymology
  • Fibroblasts / metabolism
  • Friedreich Ataxia / blood
  • Friedreich Ataxia / metabolism*
  • Glutathione / metabolism
  • Humans
  • Malondialdehyde / blood*
  • Oxidative Stress*
  • Reference Values


  • Biomarkers
  • Chlorides
  • Ferric Compounds
  • Malondialdehyde
  • Aconitate Hydratase
  • Glutathione
  • ferric chloride