Reduced d-serine levels in the nucleus accumbens of cocaine-treated rats hinder the induction of NMDA receptor-dependent synaptic plasticity

Livia Curcio, Maria V. Podda, Lucia Leone, Roberto Piacentini, Alessia Mastrodonato, Pamela Cappelletti, Silvia Sacchi, Loredano Pollegioni, Claudio Grassi, Marcello D'Ascenzo

Research output: Contribution to journalArticlepeer-review

Abstract

Cocaine seeking behaviour and relapse have been linked to impaired potentiation and depression at excitatory synapses in the nucleus accumbens, but the mechanism underlying this process is poorly understood. We show that, in the rat nucleus accumbens core, d-serine is the endogenous coagonist of N-methyl-d-aspartate receptors, and its presence is essential for N-methyl-d-aspartate receptor-dependent potentiation and depression of synaptic transmission. Nucleus accumbens core slices obtained from cocaine-treated rats after 1 day of abstinence presented significantly reduced d-serine concentrations, increased expression of the d-serine degrading enzyme, d-amino acid oxidase, and downregulated expression of serine racemase, the enzyme responsible for d-serine synthesis. The d-serine deficit was associated with impairment of potentiation and depression of glutamatergic synaptic transmission, which was restored by slice perfusion with exogenous d-serine. Furthermore, in vivo administration of d-serine directly into the nucleus accumbens core blocked behavioural sensitization to cocaine. These results provide evidence for a critical role of d-serine signalling in synaptic plasticity relevant to cocaine addiction.

Original languageEnglish
Pages (from-to)1216-1230
Number of pages15
JournalBrain
Volume136
Issue number4
DOIs
Publication statusPublished - 2013

Keywords

  • cocaine
  • D-serine
  • NMDA receptors
  • nucleus accumbens
  • synaptic plasticity

ASJC Scopus subject areas

  • Clinical Neurology

Fingerprint Dive into the research topics of 'Reduced d-serine levels in the nucleus accumbens of cocaine-treated rats hinder the induction of NMDA receptor-dependent synaptic plasticity'. Together they form a unique fingerprint.

Cite this