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Methylenedioxymethamphetamine depresses glutamate-evoked neuronal firing and increases extracellular levels of dopamine and serotonin in the nucleus accumbens in vivo.

S R White, P Duffy, P W Kalivas

Neuroscience September 1994 DOI: 10.1016/0306-4522(94)90313-1 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical experimental study Peer reviewed
Population Rats
Interventions MDMA SCH39166 p-chlorophenylalanine
Topics MDMA Serotonin
Key findings Microiontophoretic MDMA inhibited glutamate-evoked firing in 83 of 86 nucleus accumbens cells tested; this inhibition was partially blocked by the dopamine antagonist SCH39166 and attenuated by combined pretreatment with p-chlorophenylalanine and alpha-methyl-tyrosine. MDMA applied via dialysis probe increased extracellular dopamine and serotonin in the nucleus accumbens and adjacent ventral striatum, suggesting the inhibition is mediated by these increased neurotransmitter levels.

Abstract

The nucleus accumbens has been implicated as an important site for the actions of many drugs that are used recreationally. This study examined the effects of methylenedioxymethamphetamine (MDMA), a euphoric and hallucinogenic drug, on glutamate-evoked neuronal firing and on extracellular levels of dopamine and serotonin in the nucleus accumbens of the rat. Microiontophoretic application of MDMA inhibited glutamate-evoked firing of most of the nucleus accumbens cells that were tested (83 of 86), as did microiontophoretic application of dopamine and serotonin. MDMA-induced inhibition of glutamate-evoked firing was partially blocked by the dopamine antagonist SCH39166 and was attenuated by combined pretreatment with inhibitors of both serotonin and catecholamine synthesis, p-chlorophenylalanine and alpha-methyl-p-tyrosine. MDMA applied directly into the nucleus accumbens and adjacent regions of the ventral striatum through a dialysis probe increased extracellular levels of both dopamine and serotonin. These results indicate that MDMA has inhibitory effects on glutamate-evoked neuronal firing in the nucleus accumbens and suggest that the inhibition is mediated by increased extracellular dopamine and serotonin. Furthermore, these results permit MDMA to be added to the extensive list of abused drugs that have been demonstrated to elevate extracellular levels of dopamine and serotonin in the nucleus accumbens.