首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >The potential involvement of miR-204-3p-axon guidance network in methamphetamine-induced locomotor sensitization of mice
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The potential involvement of miR-204-3p-axon guidance network in methamphetamine-induced locomotor sensitization of mice

机译:miR-204-3P-AXON引导网络在甲基苯丙胺诱导的小鼠致甲羟类致甲胺的潜在累积

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MicroRNAs (miRNAs) are gene expression regulators that play an important role in drug addiction. We previously reported miR-204-3p was the only up-regulated miRNA in the nucleus accumbens (NAc) in methamphetamine (METH)-sensitized mice. In this study, we are reporting a miR-204-3p potential mechanism in METH sensitization. We first measured the expression changes of miR-204-3p in the NAc of METH- sensitized mice. Then we predicted the targets of miR-204-3p by bioinformatics tools and combined the potential targets with the METH-responsive genes from the ArrayExpress database. KEGG pathway analyses were performed to investigate the prospective mechanisms and four enriched genes were validated by RT-PCR. As a result, miR-204-3p showed a shift from down-regulation to up-regulation in the NAc from the development to the expression of METH sensitization. Bioinformatics analysis predicted 1834 putative targets, 259 of which were differentially expressed in the NAc in response to METH. These targets were significantly enriched in axon guidance (P = 9.59 x 10(-6)). Four putative targets (Sema3A, Plxna4, Rac1, and Pak3) enriched in axon guidance also exhibited significant changes in the NAc after METH challenge injection. Moreover, expression levels of miR-204-3p, Sema3A and Plxna4 exhibited a negative association in the expression of METH sensitization. It appeared that miR-204-3p may be involved in the expression of METH sensitization by regulating the expression of Sema3A and Plxna4. Our study provided a potential network of miR-204-3p-axon guidance in the NAc in the expression of METH-induced behavioral sensitization.
机译:微小RNA(miRNA)是基因表达调节是发挥药物成瘾的重要作用。我们以前报道的miR-204-3p在伏隔核的唯一上调的miRNA(NAC)的甲基苯丙胺(冰毒)致敏小鼠。在这项研究中,我们报告了METH致敏的miR-204-3p的潜在机制。我们首先测定的miR-204-3p的在甲 - 的伏隔核表达的变化致敏小鼠。然后,我们通过生物信息学工具预测的miR-204-3p的目标,并结合从ArrayExpress数据库冰毒反应基因的潜在目标。进行KEGG途径分析来调查潜在的机制和四个富集的基因通过RT-PCR进行了验证。其结果是,的miR-204-3p显示从下调到上调NAc中的从开发到METH致敏的表达的转变。生物信息学分析预测1834个推定的目标,其中259被差异NAc中的响应于METH表达。这些目标在轴突导向被显著富集的(P = 9.59×10(-6))。在轴突导向富含四个假定目标(检测Sema3A,PLXNA4与Rac1和PAK3)也表现出了伏隔核后METH注射挑战变化显著。此外,的miR-204-3p的表达水平,检测Sema3A和PLXNA4表现出致敏METH的表达呈负相关。它出现了miR-204-3p可以METH致敏的表达通过调节检测Sema3A和PLXNA4的表达有关。我们的研究在METH诱导行为敏化的表达提供的miR-204-3p轴突导向的潜在网络中的NAC。

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