Chronically administered 3-nitropropionic acid induces striatal lesions attributed to dysfunction of the blood-brain barrier

Neurosci Lett. 1995 Feb 17;186(2-3):161-4. doi: 10.1016/0304-3940(95)11311-j.

Abstract

3-Nitropropionic acid (3-NPA), an irreversible inhibitor of succinate dehydrogenase, was administered to rats and the characteristics of the neuronal damage were investigated. Injections of 3-NPA (15 mg/kg s.c.) every 2 or 3 days for 1-2 weeks induced a mild neuronal loss and neutrophil invasions in the striatum (STR). The same administration for 4 weeks induced specific symmetric lesions in the lateral STR although the size was variable in each animal. Inside the lesions, strong neutrophil invasions and a strong immunoreaction for IgG, C3 as well as complement factor C3b/C4b receptor (C3b/C4br) were detected. Lesioned sites lost the immunoreaction for GFAP while the marginal areas contained abundant GFAP-labeled astrocytes around the vessels. In intoxicated animals, there was a weak but stout immunoreaction for IgG and C3b/C4br localizing around vessels in the STR even when there were no lesions or neuronal loss. The data suggest that the blood-brain barrier dysfunction is responsible for the specific vulnerability of the STR for the toxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antihypertensive Agents / toxicity*
  • Blood-Brain Barrier / drug effects*
  • Brain Diseases / chemically induced
  • Brain Diseases / pathology*
  • Complement C3b / metabolism
  • Complement C4b / metabolism
  • Glial Fibrillary Acidic Protein / metabolism
  • Immunoglobulin G
  • Immunohistochemistry
  • Male
  • Neostriatum / pathology*
  • Nerve Degeneration / drug effects
  • Nitro Compounds
  • Propionates / toxicity*
  • Rats
  • Rats, Wistar

Substances

  • Antihypertensive Agents
  • Glial Fibrillary Acidic Protein
  • Immunoglobulin G
  • Nitro Compounds
  • Propionates
  • Complement C3b
  • Complement C4b
  • 3-nitropropionic acid