Dopamine-glutamate interactions in methamphetamine-induced neurotoxicity

J Neural Transm Gen Sect. 1993;91(2-3):241-54. doi: 10.1007/BF01245234.

Abstract

Repeated administration of methamphetamine (m-AMPH) to rats induces dopamine (DA) terminal damage, and coadministration of antagonists of the N-methyl-D-aspartate (NMDA) or dopamine D1 or D2 receptors are protective. Striatal microdialysis of rats given a neurotoxic regimen of 4 x m-AMPH (4 mg/kg, s.c.) treatments revealed a dramatic and prolonged elevation of extracellular DA after the final m-AMPH administration. Neuroprotective regimens of MK-801, SCH 23390, or eticlopride greatly attenuated the overflow of DA resulting from the fourth m-AMPH treatment. By itself, MK-801 had no significant influence on striatal DA overflow, whereas either DA antagonist given alone elevated dialysate DA concentrations. A significant correlation was found between the magnitude of the m-AMPH-induced DA overflow of individual microdialyzed rats and their striatal DA content at sacrifice one week later. We conclude that the ability of non-competitive NMDA antagonists and of the D1 or D2 antagonists to protect against m-AMPH-induced striatal DA terminal injury can be accounted for by their attenuation of m-AMPH-evoked DA overflow. These findings underscore the important role played by elevated extracellular DA concentrations to the injurious effects of this stimulant drug.

Publication types

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

MeSH terms

  • Animals
  • Benzazepines / pharmacology
  • Chromatography, High Pressure Liquid
  • Corpus Striatum / drug effects*
  • Corpus Striatum / metabolism
  • Dialysis
  • Dizocilpine Maleate / pharmacology
  • Dopamine / metabolism*
  • Dopamine Antagonists*
  • Glutamates / metabolism*
  • Glutamic Acid
  • Male
  • Methamphetamine / antagonists & inhibitors
  • Methamphetamine / pharmacology
  • Methamphetamine / toxicity*
  • Microchemistry
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Dopamine / classification
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
  • Salicylamides / pharmacology

Substances

  • Benzazepines
  • Dopamine Antagonists
  • Glutamates
  • Receptors, Dopamine
  • Receptors, N-Methyl-D-Aspartate
  • Salicylamides
  • Glutamic Acid
  • Methamphetamine
  • Dizocilpine Maleate
  • eticlopride
  • Dopamine