The inflammatory reaction following 1-methyl-4-phenyl-1,2,3, 6-tetrahydropyridine intoxication in mouse

Exp Neurol. 1999 Mar;156(1):50-61. doi: 10.1006/exnr.1998.6993.

Abstract

In degenerative disorders of the CNS an immune system involvement in the pathological process is postulated. The MPTP model of Parkinson's disease seem to be a good model for studying an inflammation following toxic neurodegeneration. In this model, microglial and astroglial reactions were previously found around impaired neurons. In the present work we showed an immune reaction, including lymphocytic infiltration of CD4+ and CD8+ T cells in the substantia nigra and striatum and elevated MHC class I and II antigens expression on microglia. Many activated lymphocytes were present, showing increased LFA-1 and CD44 antigen expression. We found also that ICAM-1 expression increased on the endothelium and appeared on microglia in the injured regions. Treatment with dexamethasone inhibited T-cell infiltration and MHC class II expression, lessened the glial reaction, and also diminished neuronal impairment. These findings suggest that an immune mechanism may contribute to the neuronal damage following MPTP administration.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Dexamethasone / pharmacology
  • Dopamine / physiology
  • Dopamine Agents / toxicity*
  • Glial Fibrillary Acidic Protein / biosynthesis
  • Histocompatibility Antigens Class I / biosynthesis
  • Histocompatibility Antigens Class II / biosynthesis
  • Immunoglobulin G / metabolism
  • Immunohistochemistry
  • Inflammation / chemically induced
  • Inflammation / immunology*
  • Intercellular Adhesion Molecule-1 / metabolism
  • Lymphocyte Activation
  • MPTP Poisoning*
  • Mice
  • Mice, Inbred C57BL
  • Microglia / metabolism
  • Neostriatum / drug effects
  • Neostriatum / metabolism
  • Nerve Degeneration / immunology
  • Neuroglia / metabolism
  • Substantia Nigra / drug effects
  • Substantia Nigra / metabolism
  • T-Lymphocytes / immunology

Substances

  • Anti-Inflammatory Agents
  • Dopamine Agents
  • Glial Fibrillary Acidic Protein
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • Immunoglobulin G
  • Intercellular Adhesion Molecule-1
  • Dexamethasone
  • Dopamine