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Evidence for Neuronal Origin and Metabotropic Receptor‐Mediated Regulation of Extracellular Glutamate and Aspartate in Rat Striatum In Vivo Following Electrical Stimulation of the Prefrontal Cortex
Author(s) -
Lada Mark W.,
Vickroy Thomas W.,
Kennedy Robert T.
Publication year - 1998
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1998.70020617.x
Subject(s) - metabotropic glutamate receptor , neuroscience , stimulation , striatum , metabotropic glutamate receptor 5 , glutamate receptor , metabotropic receptor , prefrontal cortex , chemistry , extracellular , in vivo , metabotropic glutamate receptor 8 , biology , receptor , biochemistry , dopamine , cognition , microbiology and biotechnology
Extracellular levels of glutamate (Glu) and aspartate (Asp) were measured at 5‐s intervals in the striatum of chloral hydrate‐anesthetized rats by using microdialysis coupled to an automated assay system based on capillary electrophoresis with laser‐induced fluorescence. Application of a single 10‐s train of depolarizing pulses to the prefrontal cortex caused a rapid increase in Glu and Asp concentrations (200–300% of basal value), which returned to basal level within 60 s. The stimulated rise in Glu and Asp concentrations was blocked completely by 2 µ M tetrodotoxin or depletion of extracellular Ca 2+ , suggesting a neuronal origin of the Glu and Asp. Infusion of the Glu transport inhibitor l ‐ trans ‐pyrrolidine‐2,4‐dicarboxylic acid (200 µ M ) increased resting Glu and Asp levels by 300–500% without altering electrically stimulated changes in Glu and Asp concentration. Stimulated Glu and Asp concentration changes were suppressed by 91 and 73%, respectively, by the metabotropic Glu receptor agonist (1 S ,3 R )‐1‐aminocyclopentane‐ trans ‐1,3‐dicarboxylate (200 µ M ). This effect was blocked by the metabotropic Glu receptor antagonist ( RS )‐α‐methylcarboxyphenylglycine (MCPG; 200 µ M ). MCPG alone produced no effect on electrically stimulated changes in Glu and Asp levels; however, in the presence of l ‐ trans ‐pyrrolidine‐2,4‐dicarboxylic acid, MCPG produced a five‐ to sixfold increase in stimulated overflow. Based on these results, it is concluded that release of Glu and Asp from corticostriatal neurons can be inhibited by activation of metabotropic Glu autoreceptors, which may be an important determinant of excitatory transmission at striatal synapses.