Yuferov Vadim, Zhang Yong, Liang Yupu, Zhao Connie, Randesi Matthew, Kreek Mary J
Laboratory of the Biology of Addictive Diseases, The Rockefeller University, New York, NY, United States.
Research Bioinformatics, Clinical and Translational Science Award, The Rockefeller University, New York, NY, United States.
Front Psychiatry. 2018 Jun 12;9:257. doi: 10.3389/fpsyt.2018.00257. eCollection 2018.
Oxycodone is one a commonly used medication for pain, and is also a widely abused prescription opioid, like other short-acting MOPr agonists. Neurochemical and structural adaptations in brain following chronic MOPr-agonist administration are thought to underlie pathogenesis and persistence of opiate addiction. Many axon guidance molecules, such as integrins, semaphorins, and ephrins may contribute to oxycodone-induced neuroadaptations through alterations in axon-target connections and synaptogenesis, that may be implicated in the behaviors associated with opiate addiction. However, little is known about this important area. The aim of this study is to investigate alterations in expression of selected integrin, semaphorin, ephrins, netrin, and slit genes in the nucleus accumbens (NAc) and caudate putamen (CPu) of mice following extended 14-day oxycodone self-administration (SA), using RNAseq. Total RNA from the NAc and CPu were isolated from adult male C57BL/6J mice within 1 h after the last session of oxycodone in a 14-day self-administration paradigm (4h/day, 0.25 mg/kg/infusion, FR1) or from yoked saline controls. Gene expressions were examined using RNA sequencing (RNA-Seq) technology. RNA-Seq libraries were prepared using Illumina's TruSeq® Stranded Total RNA LT kit. The reads were aligned to the mouse reference genome (version mm10) using STAR. DESeq2 was applied to the counts of protein coding genes to estimate the fold change between the treatment groups. False Discovery Rate (FDR) < 0.1 were used to select genes that have a significant expression change. For selection of a subset of genes related to axon guidance pathway, REACTOME was used. Among 38 known genes of the integrin, semaphorin, and ephrin gene families, RNA-seq data revealed up-regulation of six genes in the NAc: heterodimer receptor, integrins , and , and its ligand semaphorin , two semaphorin receptors, plexins and . There was down-regulation of eight genes in this region: two integrin genes and , semaphorins , semaphorin receptor neuropilin , and ephrin receptor . In the CPu, there were five differentially expressed axon guidance genes: up-regulation of three integrin genes, , and down-regulation of and ephrin were thus observed. No significant alterations in expression of Netrin-1 or Slit were observed. We provide evidence for alterations in the expression of selective axon guidance genes in adult mouse brain following chronic self-administration of oxycodone. Further examination of oxycodone-induced changes in the expression of these specific axon guidance molecules and integrin genes in relation to behavior may provide new insights into development of addiction to oxycodone.
羟考酮是一种常用的镇痛药,与其他短效μ阿片受体激动剂一样,也是一种被广泛滥用的处方类阿片。长期使用μ阿片受体激动剂后大脑中的神经化学和结构适应性变化被认为是阿片类药物成瘾的发病机制和持续性的基础。许多轴突导向分子,如整合素、信号素和 Ephrin 蛋白,可能通过改变轴突与靶标的连接和突触形成,导致羟考酮诱导的神经适应性变化,这可能与阿片类药物成瘾相关的行为有关。然而,关于这一重要领域的了解甚少。本研究的目的是使用RNA测序技术,研究成年雄性C57BL/6J小鼠在14天延长的羟考酮自我给药(SA)后,伏隔核(NAc)和尾状壳核(CPu)中选定的整合素、信号素、Ephrin 蛋白、网蛋白和 Slit 基因的表达变化。在14天自我给药范式(每天4小时,0.25毫克/千克/输注,固定比率1)的最后一次羟考酮给药后1小时内,从成年雄性C57BL/6J小鼠的NAc和CPu中分离总RNA,或从配对的生理盐水对照组中分离。使用RNA测序(RNA-Seq)技术检测基因表达。使用Illumina的TruSeq®链特异性总RNA LT试剂盒制备RNA-Seq文库。使用STAR将读数与小鼠参考基因组(版本mm10)进行比对。将DESeq2应用于蛋白质编码基因的计数,以估计治疗组之间的倍数变化。使用错误发现率(FDR)<0.1来选择具有显著表达变化的基因。为了选择与轴突导向途径相关的基因子集,使用了REACTOME。在整合素、信号素和Ephrin基因家族的38个已知基因中,RNA测序数据显示NAc中有6个基因上调:异二聚体受体整合素α3β1、α5β1及其配体信号素3A、两个信号素受体丛蛋白A1和A2。该区域有8个基因下调:两个整合素基因α1和α2、信号素3B、信号素受体神经纤毛蛋白1和Ephrin受体EphB1。在CPu中,有5个差异表达的轴突导向基因:3个整合素基因α1、α3和α5上调,α2和Ephrin B2下调。未观察到网蛋白-1或Slit表达的显著变化。我们提供了慢性自我给药羟考酮后成年小鼠大脑中选择性轴突导向基因表达变化的证据。进一步研究羟考酮诱导的这些特定轴突导向分子和整合素基因表达变化与行为的关系,可能为羟考酮成瘾的发展提供新的见解。