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SELF ADMINISTRATION OF OXYCODONE ALTERS SYNAPTIC PLASTICITY GENE EXPRESSION IN THE HIPPOCAMPUS DIFFERENTIALLY IN MALE ADOLESCENT AND ADULT MICE
Zhang Y; Brownstein AJ; Buonora M; Niikura K; Ho A; da Rosa JC; Kreek MJ; Ott J
通讯作者邮箱zhangyo@rockefeller.edu
心理所单位排序4
摘要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.
关键词oxycodone self-administration adult hippocampus adolescent synaptic plasticity gene expression
学科领域生理心理学/生物心理学
2015
语种英语
DOI10.1016/j.neuroscience.2014.11.013
发表期刊Neuroscience
卷号285期号:1页码:34-46
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收录类别SCI
资助项目NIH 1R01DA029147 (YZ) ; Dr. Miriam and Sheldon G. Adelson Medical Research Foundation (MJK)
资助机构NIH ; Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
引用统计
被引频次:33[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.psych.ac.cn/handle/311026/10194
专题健康与遗传心理学研究室
通讯作者Zhang Y
推荐引用方式
GB/T 7714
Zhang Y,Brownstein AJ,Buonora M,et al. SELF ADMINISTRATION OF OXYCODONE ALTERS SYNAPTIC PLASTICITY GENE EXPRESSION IN THE HIPPOCAMPUS DIFFERENTIALLY IN MALE ADOLESCENT AND ADULT MICE[J]. Neuroscience,2015,285(1):34-46.
APA Zhang Y.,Brownstein AJ.,Buonora M.,Niikura K.,Ho A.,...&Ott J.(2015).SELF ADMINISTRATION OF OXYCODONE ALTERS SYNAPTIC PLASTICITY GENE EXPRESSION IN THE HIPPOCAMPUS DIFFERENTIALLY IN MALE ADOLESCENT AND ADULT MICE.Neuroscience,285(1),34-46.
MLA Zhang Y,et al."SELF ADMINISTRATION OF OXYCODONE ALTERS SYNAPTIC PLASTICITY GENE EXPRESSION IN THE HIPPOCAMPUS DIFFERENTIALLY IN MALE ADOLESCENT AND ADULT MICE".Neuroscience 285.1(2015):34-46.
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