Role of dietary iron restriction in a mouse model of Parkinson's disease

Exp Neurol. 2004 Dec;190(2):506-14. doi: 10.1016/j.expneurol.2004.08.014.

Abstract

There is a growing body of evidence suggesting that iron chelation may be a useful therapy in the treatment of Parkinson's Disease (PD). Experiments were designed to test the impact of dietary iron availability on the pathogenic process and functional outcome in a mouse model of PD. Mice were fed diets containing low (4 ppm) or adequate (48 ppm) amounts of iron for 6 weeks before the administration of MPTP, a mitochondrial toxin that damages nigrostriatal dopaminergic neurons and induces Parkinson-like symptoms. Low dietary iron increased serum total iron binding capacity (P < 0.001). Consistent with neuronal protection, iron restriction increased sphingomyelin C16:0 and decreased ceramide C16:0. However, there was a 35% decrease in striatal dopamine (DA) in iron-restricted mice. Motor behavior was also impaired in these animals. In vitro studies suggested that severe iron restriction could lead to p53-mediated neuronal apoptosis. Administration of MPTP reduced striatal DA (P < 0.01) and impaired motor behavior in iron-adequate mice. However, in iron-restricted mice, striatal dopamine levels and motor behavior were unchanged compared to saline-treated mice. Thus, while reduced iron may provide protection against PD-inducing insults such as MPTP, the role of iron in the synthesis of DA and neuronal survival should be considered, particularly in the development of iron-chelating agents to be used chronically in the clinical setting.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / physiology
  • Cells, Cultured
  • Ceramides / metabolism
  • Corpus Striatum / drug effects*
  • Corpus Striatum / pathology
  • Dopamine / metabolism
  • Immunohistochemistry
  • Iron, Dietary / pharmacology*
  • MPTP Poisoning / physiopathology*
  • Male
  • Mice
  • Microscopy, Confocal
  • Motor Activity / drug effects
  • Motor Activity / physiology
  • Neurons / drug effects
  • Neurons / pathology
  • Sphingomyelins / metabolism
  • Tumor Suppressor Protein p53 / drug effects
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Ceramides
  • Iron, Dietary
  • Sphingomyelins
  • Tumor Suppressor Protein p53
  • Dopamine