Demirel Goksun, Guzel Esra, Creighton Chad J, Ozturk Yeter Erol, Kucuk Ceyhun, Asliyuksek Hızır, Yurdun Türkan
Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Biruni University, Istanbul, Turkey.
Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Çukurova University, Adana, Turkey.
Iran J Pharm Res. 2019 Fall;18(4):1989-1999. doi: 10.22037/ijpr.2019.15097.12874.
3,4-methylenedioxymethamphetamine (MDMA) is one of the most widespread illegal drugs, that have been used particularly by young people in the 15-34 age group. MicroRNAs (miRNAs) are endogenously synthesized, non-coding, and small RNAs that post-transcriptionally regulate their target genes' expression by inhibiting protein translation or degradation. miRNAs are increasingly implicated in drug-related gene expressions and functions. Notably, there are no reports of miRNA variation in the human brain in MDMA abuse. We here present a miRNA profiling study - the first such study, to the best of our knowledge - into the post-mortem human brains of a sample of people with MDMA abuse, along with non-drug dependent controls. The miRNA profiling of nucleus accumbens (NAc) and ventral tegmental areas (VTA) was performed by microarray analysis. Subsequently, two candidate miRNA putative biomarkers were selected according to significant regional differential expression (miR-1202 and miR-7975), using quantitative reverse-transcription PCR (qRT-PCR). We showed that the expression level of miR-7975 was significantly lower in the VTA regions of the 30 MDMA users, as compared with the 30 control samples. Another significantly deregulated miR-1202 was down-regulated in the NAc regions of 30 MDMA samples in comparison to the control samples. Alteration of these miRNAs can potentially serve as novel biomarkers for MDMA abuse, and warrant further research in independent and larger samples of patients.
3,4-亚甲基二氧甲基苯丙胺(摇头丸)是最普遍使用的非法药物之一,尤其在15至34岁的年轻人中被使用。微小RNA(miRNA)是内源性合成的非编码小RNA,通过抑制蛋白质翻译或降解在转录后调节其靶基因的表达。miRNA越来越多地涉及与药物相关的基因表达和功能。值得注意的是,尚无关于摇头丸滥用者人脑miRNA变异的报道。在此,我们进行了一项miRNA谱研究——据我们所知这是第一项此类研究——针对一组摇头丸滥用者的尸检人脑以及非药物依赖对照。通过微阵列分析对伏隔核(NAc)和腹侧被盖区(VTA)进行miRNA谱分析。随后,根据显著的区域差异表达(miR-1202和miR-7975),使用定量逆转录PCR(qRT-PCR)选择了两个候选miRNA假定生物标志物。我们发现,与30个对照样本相比,30名摇头丸使用者的VTA区域中miR-7975的表达水平显著降低。与对照样本相比,另一个显著失调的miR-1202在30个摇头丸样本的NAc区域中下调。这些miRNA的改变可能作为摇头丸滥用的新型生物标志物,值得在独立且更大的患者样本中进一步研究。