Participation of par-4 in the degeneration of striatal neurons induced by metabolic compromise with 3-nitropropionic acid

Exp Neurol. 2000 Sep;165(1):1-11. doi: 10.1006/exnr.2000.7434.

Abstract

Huntington's disease (HD) is a progressive neurodegenerative disorder characterized by chorea, psychiatric disturbances, and dementia. It is caused by a polyglutamine repeat expansion in the huntingtin protein. The striatum is a major site of neuronal loss in HD, but the mechanisms underlying the neurodegenerative process have not been established. Systemic administration of the succinate dehydrogenase inhibitor 3-nitropropionic acid (3NP) to rodents results in motor dysfunction and degeneration of striatal neurons with features similar to those of HD. Here we report that levels of prostate apoptosis response-4 (Par-4; a protein recently linked to neuronal apoptosis) increase in striatum, and to a lesser extent in cortex and hippocampus, after systemic administration of 3NP to adult rats. The increase in Par-4 levels occurred within 6 h of 3NP administration and was followed by an increase in caspase activation which preceded neuronal loss. Exposure of cultured primary striatal neurons to 3NP induced a rapid increase of Par-4 levels and caspase activation. Treatment of striatal neurons with a Par-4 antisense oligonucleotide blocked Par-4 induction by 3NP, suppressed caspase activation, and attenuated neuronal apoptosis. The caspase-3 inhibitor DEVD suppressed 3NP-induced apoptosis of striatal neurons, but did not prevent induction of Par-4, indicating that Par-4 acts upstream of caspase-3 activation in the cell death pathway. Our results suggest that Par-4 plays an important role in the degeneration of striatal neurons in an experimental model of HD.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Apoptosis Regulatory Proteins
  • Carrier Proteins / metabolism
  • Carrier Proteins / physiology*
  • Caspases / metabolism
  • Corpus Striatum / metabolism
  • Corpus Striatum / pathology
  • Corpus Striatum / physiopathology*
  • Enzyme Activation
  • Intracellular Signaling Peptides and Proteins*
  • Male
  • Nerve Degeneration / physiopathology*
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / physiology*
  • Neurotoxins / pharmacology*
  • Nitro Compounds
  • Propionates / pharmacology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Apoptosis Regulatory Proteins
  • Carrier Proteins
  • Intracellular Signaling Peptides and Proteins
  • Neurotoxins
  • Nitro Compounds
  • Propionates
  • prostate apoptosis response-4 protein
  • Caspases
  • 3-nitropropionic acid