Extinction-dependent alterations in corticostriatal mGluR2/3 and mGluR7 receptors following chronic methamphetamine self-administration in rats

• Published in: PloS one 2012-03, Vol.7 (3), p.e34299
• Main Authors: Schwendt, Marek, Reichel, Carmela M, See, Ronald E
• Format: Article
• Language: English
• Subjects: Alcohol; Amphetamines; Animal cognition; Animals; Biology; Biotin; Caudate-putamen; Cerebral Cortex - drug effects; Circuits; Cognition - drug effects; Cognitive ability; Cognitive disorders; Corpus Striatum - drug effects; Cortex; Drug abuse; Drug dosages; Extinction; Extinction, Psychological - drug effects; Gene Expression Regulation - drug effects; Glutamate; Glutamic acid receptors (metabotropic); Laboratory animals; Learning; Male; Medicine; Memory; Methamphetamine; Methamphetamine - administration & dosage; Motivation - drug effects; Neostriatum; Neurotransmission; Nucleus accumbens; Prefrontal cortex; Prefrontal Cortex - drug effects; Psychosis; Rats; Rats, Long-Evans; Receptors; Receptors, Metabotropic Glutamate - metabolism; Rodents; Schizophrenia; Self Administration; Serotonin; Substance abuse treatment; Surgery; Sympathomimetics - administration & dosage; Synaptosomes
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0034299

Methamphetamine (meth) is a highly addictive and widely abused psychostimulant. Repeated use of meth can quickly lead to dependence, and may be accompanied by a variety of persistent psychiatric symptoms and cognitive impairments. The neuroadaptations underlying motivational and cognitive deficits produced by chronic meth intake remain poorly understood. Altered glutamate neurotransmission within the prefrontal cortex (PFC) and striatum has been linked to both persistent drug-seeking and cognitive dysfunction. Therefore, the current study investigated changes in presynaptic mGluR receptors within corticostriatal circuitry after extended meth self-administration. Rats self-administered meth (or received yoked-saline) in 1 hr/day sessions for 7 days (short-access) followed by 14 days of 6 hrs/day (long-access). Rats displayed a progressive escalation of daily meth intake up to 6 mg/kg per day. After cessation of meth self-administration, rats underwent daily extinction or abstinence without extinction training for 14 days before being euthanized. Synaptosomes from the medial PFC, nucleus accumbens (NAc), and the dorsal striatum (dSTR) were isolated and labeled with membrane-impermeable biotin in order to measure surface mGluR2/3 and mGluR7 receptors. Extended access to meth self-administration followed by abstinence decreased surface and total levels of mGluR2/3 receptors in the NAc and dSTR, while in the PFC, only a loss of surface mGluR2/3 and mGluR7 receptors was detected. Daily extinction trials reversed the downregulation of mGluR2/3 receptors in the NAc and dSTR and mGluR7 in the PFC, but downregulation of surface mGluR2/3 receptors in the PFC was present regardless of post-meth experience. Thus, extinction learning can selectively restore some populations of downregulated mGluRs after prolonged exposure to meth. The present findings could have implications for our understanding of the persistence (or recovery) of meth-induced motivational and cognitive deficits.