Cell-type specificity of mGluR activation in striatal neuronal subtypes

Amino Acids. 2000;19(1):119-29. doi: 10.1007/s007260070040.

Abstract

The effects of metabotropic glutamate receptor (mGluR) activation were studied in medium spiny neurons and large aspiny (LA) interneurons by means of electrophysiological and optical recordings. DCG-IV and L-SOP, agonists for group II and III mGluRs, respectively, produced a presynaptic inhibitory effect on corticostriatal glutamatergic excitatory postsynaptic potentials (EPSPs) in both spiny and LA cells. Activation of group I mGluRs by the selective agonist 3,5-DHPG produced no effect on membrane properties and glutamatergic transmission in spiny neurons, whereas it did cause a membrane depolarization in LA interneurons coupled to increased input resistance. In combined optical and electrophysiological experiments, in spiny neurons 3,5-DHPG enhanced membrane depolarization and intracellular calcium (Ca2+) levels induced by NMDA applications, but not in LA interneurons. These data suggest the existence of a positive interaction between NMDA and group I mGlu receptors only in medium spiny cells which might, at least partially, account for the differential vulnerability to excitotoxic damage observed in striatal neuronal subtypes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Corpus Striatum / cytology
  • Corpus Striatum / metabolism*
  • Corpus Striatum / physiology
  • Excitatory Amino Acid Agonists / pharmacology
  • Excitatory Postsynaptic Potentials
  • Glycine / analogs & derivatives
  • Glycine / pharmacology
  • Male
  • Neurons / metabolism*
  • Neurons / physiology
  • Rats
  • Rats, Wistar
  • Receptors, Metabotropic Glutamate / agonists*
  • Receptors, Metabotropic Glutamate / metabolism
  • Resorcinols / pharmacology

Substances

  • Excitatory Amino Acid Agonists
  • Receptors, Metabotropic Glutamate
  • Resorcinols
  • 3,5-dihydroxyphenylglycine
  • Glycine