Age dependence of striatal neuronal death caused by mitochondrial dysfunction

Neuroreport. 1993 Jan;4(1):73-6. doi: 10.1097/00001756-199301000-00019.

Abstract

Several lines of evidence point to a decline in mitochondrial efficiency with age. The relationship between age and sensitivity to Huntington disease-like neuronal death in the striatum induced by the mitochondrial inhibitor 3-nitropropionic acid (3-NP) was examined. 3-NP has been shown to cause degeneration of striatum, hippocampus, and thalamus in rat and of caudate-putamen in humans. We administered single doses of 3-NP intraperitoneally to rats of various ages. Animals older than 4 months exhibited a far greater susceptibility to striatal neurotoxicity and mortality compared with younger animals. These results are discussed in the context of age-dependent metabolic impairment, which may be a key factor in the etiology of neurodegenerative disorders such as Huntington's disease and Alzheimer's disease.

Publication types

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

MeSH terms

  • Acetylcholinesterase / metabolism
  • Aging / physiology*
  • Animals
  • Cell Death / drug effects
  • Cell Death / physiology
  • Corpus Striatum / cytology
  • Corpus Striatum / pathology*
  • Histocytochemistry
  • Male
  • Mitochondria / drug effects
  • Mitochondria / enzymology
  • Mitochondria / physiology*
  • Nitro Compounds
  • Oxygen Consumption / drug effects
  • Oxygen Consumption / physiology
  • Propionates / pharmacology
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Nitro Compounds
  • Propionates
  • Acetylcholinesterase
  • 3-nitropropionic acid