Self administration of oxycodone alters synaptic plasticity gene expression in the hippocampus differentially in male adolescent and adult mice. (29th January 2015)

• Record Type: Journal Article
• Authors: Zhang, Y.; Brownstein, A.J.; Buonora, M.; Niikura, K.; Ho, A.; Correa da Rosa, J.; Kreek, M.J.; Ott, J.
• Is Part Of: Neuroscience. Volume 285(2015)
• Page Start: 34
• Page End: 46
• Publication Date: 2015-01-29
• Subjects: LTP long-term potentiation -- MOP-r Mu opioid receptor -- PCR polymerase chain reaction; oxycodone self-administration -- hippocampus -- synaptic plasticity -- gene expression -- adult -- adolescent; Neurochemistry -- Periodicals; Neurophysiology -- Periodicals; Neurology -- Periodicals; Neurochimie -- Périodiques; Neurophysiologie -- Périodiques; Neurochemistry; Neurophysiology; Electronic journals; Periodicals; Electronic journals; 612.8
• DOI: 10.1016/j.neuroscience.2014.11.013
• Languages: English
• ISSNs: 0306-4522

Abstract

Highlights: Adolescent and adult control mice significantly differed in Mapk1, Camk2g, Gria2, Grm5 . Oxycodone SA increased hippocampal Pim1 and Art1 mRNA levels. Cdh2 and Crem mRNA significantly differed between oxycodone and saline adult mice. Abstract: Abuse and addiction to prescription opioids such as oxycodone (a short-acting Mu opioid receptor (MOP-r) agonist) in adolescence is a pressing public health issue. We have previously shown differences in oxycodone self-administration behaviors between adolescent and adult C57BL/6J mice and expression of striatal neurotransmitter receptor genes, in areas involved in reward. In this study, we aimed to determine whether oxycodone self-administration differentially affects genes regulating synaptic plasticity in the hippocampus of adolescent compared to adult mice, since the hippocampus may be involved in learning aspects associated with chronic drug self administration. Hippocampus was isolated for mRNA analysis from mice that had self administered oxycodone (0.25 mg/kg/infusion) 2 h/day for 14 consecutive days or from yoked saline controls. Gene expression was analyzed with real-time polymerase chain reaction (PCR) using a commercially available "synaptic plasticity" PCR array containing 84 genes. We found that adolescent and adult control mice significantly differed in the expression of several genes in the absence of oxycodone exposure, including those coding for mitogen-activated protein kinase, calcium/calmodulin-dependent protein kinase II gamma subunit, glutamate receptor, ionotropic AMPA2 and metabotropic 5. Chronic oxycodone self administration increased proviral integration site 1 ( Pim1 ) and thymoma viral proto-oncogene 1 mRNA levels compared to controls in both age groups. Both Pim1 and cadherin 2 mRNAs showed a significant combined effect of Drug Condition and Age × Drug Condition. Furthermore, the mRNA levels of both cadherin 2 and cAMP response element modulators showed an experiment-wise significant difference between oxycodone and saline control in adult but not in adolescent mice. Overall, this study demonstrates for the first time that chronic oxycodone self-administration differentially alters synaptic plasticity gene expression in the hippocampus of adolescent and adult mice.