The metabotropic glutamate 5 receptor modulates extinction and reinstatement of methamphetamine-seeking in mice

Rose Chesworth, Robyn M. Brown, Jee Hyun Kim, Andrew J. Lawrence

Research output: Contribution to journalArticlepeer-review

46 Citations (Scopus)

Abstract

Methamphetamine (METH) is a highly addictive psychostimulant with no therapeutics registered to assist addicts in discontinuing use. Glutamatergic dysfunction has been implicated in the development and maintenance of addiction. We sought to assess the involvement of the metabotropic glutamate 5 receptor (mGlu5) in behaviours relevant to METH addiction because this receptor has been implicated in the actions of other drugs of abuse, including alcohol, cocaine and opiates. mGlu5 knockout (KO) mice were tested in intravenous self-administration, conditioned place preference and locomotor sensitization. Self-administration of sucrose was used to assess the response of KO mice to a natural reward. Acquisition and maintenance of self-administration, as well as the motivation to self-administer METH was intact in mGlu5 KO mice. Importantly, mGlu5 KO mice required more extinction sessions to extinguish the operant response for METH, and exhibited an enhanced propensity to reinstate operant responding following exposure to drug-associated cues. This phenotype was not present when KO mice were tested in an equivalent paradigm assessing operant responding for sucrose. Development of conditioned place preference and locomotor sensitization were intact in KO mice; however, conditioned hyperactivity to the context previously paired with drug was elevated in KO mice. These data demonstrate a role for mGlu5 in the extinction and reinstatement of METH-seeking, and suggests a role for mGlu5 in regulating contextual salience.
Original languageEnglish
Article numbere68371
Number of pages11
JournalPLoS One
Volume8
Issue number7
Publication statusPublished - 4 Jul 2013

Keywords

  • extinction
  • glutamate
  • methamphetamine
  • mice as laboratory animals
  • psychotropic drugs
  • receptors

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