The mitochondrial toxin, 3-nitropropionic acid, induces extracellular Zn2+ accumulation in rat hippocampus slices

Neurosci Lett. 2004 Nov 11;370(2-3):118-22. doi: 10.1016/j.neulet.2004.08.027.

Abstract

3-nitropropionic acid (3-NPA), a suicide inhibitor of succinate dehydrogenase (SDH; complex II), has been used to provide useful experimental models of Huntington's disease (HD) and "chemical hypoxia" in rodents. The trace ion Zn2+ has been shown to cause neurodegeneration. Employing real-time Newport Green fluorescence imaging of extracellular Zn2+, we found that 3-NPA (10-100 microM) caused a concentration-dependent increase in the concentration of extracellular Zn2+ ([Zn2+]o) in acute rat hippocampus slices. This increase in [Zn2+]o was abolished by 10 mM CaEDTA. The increase of [Zn2+]o was also accompanied by a rapid increase of cytoplasmic-free Zn2+ concentration ([Zn2+]i). The induction of Zn2+ release by 3-MPA in hippocampus slices points to a potential mechanism by which 3-NPA might induce neurodegeneration.

Publication types

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

MeSH terms

  • Animals
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Edetic Acid / pharmacology
  • Extracellular Space / drug effects*
  • Hippocampus / drug effects*
  • Hippocampus / metabolism
  • In Vitro Techniques
  • Microscopy, Fluorescence / methods
  • Nitro Compounds
  • Propionates / pharmacology*
  • Rats
  • Succinate Dehydrogenase / antagonists & inhibitors*
  • Time Factors
  • Zinc / metabolism*

Substances

  • Nitro Compounds
  • Propionates
  • Edetic Acid
  • Succinate Dehydrogenase
  • Zinc
  • 3-nitropropionic acid