The transition metals copper and iron in neurodegenerative diseases

Chem Biol Interact. 2010 Jul 30;186(2):184-99. doi: 10.1016/j.cbi.2010.04.010. Epub 2010 May 14.

Abstract

Neurodegenerative diseases constitute a worldwide health problem. Metals like iron and copper are essential for life, but they are also involved in several neurodegenerative mechanisms such as protein aggregation, free radical generation and oxidative stress. The role of Fe and Cu, their pathogenic mechanisms and possible therapeutic relevance are discussed regarding four of the most common neurodegenerative diseases, Alzheimer's, Parkinson's and Huntington's diseases as well as amyotrophic lateral sclerosis. Metal-mediated oxidation by Fenton chemistry is a common feature for all those disorders and takes part of a self-amplifying damaging mechanism, leading to neurodegeneration. The interaction between metals and proteins in the nervous system seems to be a crucial factor for the development or absence of neurodegeneration. The present review also deals with the therapeutic strategies tested, mainly using metal chelating drugs. Metal accumulation within the nervous system observed in those diseases could be the result of compensatory mechanisms to improve metal availability for physiological processes.

Publication types

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

MeSH terms

  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / etiology
  • Alzheimer Disease / metabolism
  • Amyotrophic Lateral Sclerosis / drug therapy
  • Amyotrophic Lateral Sclerosis / etiology
  • Amyotrophic Lateral Sclerosis / metabolism
  • Carrier Proteins / metabolism
  • Chelating Agents / therapeutic use
  • Copper / metabolism*
  • Homeostasis
  • Humans
  • Huntington Disease / drug therapy
  • Huntington Disease / etiology
  • Huntington Disease / metabolism
  • Iron / metabolism*
  • Models, Biological
  • Neurodegenerative Diseases / etiology
  • Neurodegenerative Diseases / metabolism*
  • Parkinson Disease / drug therapy
  • Parkinson Disease / etiology
  • Parkinson Disease / metabolism

Substances

  • Carrier Proteins
  • Chelating Agents
  • Copper
  • Iron