Kim Juhwan, Im Heh-In, Moon Changjong
Department of Veterinary Anatomy and Animal Behavior, College of Veterinary Medicine and BK21 Plus Project Team, Chonnam National University, Gwangju; Center for Neuroscience, Korea Institute of Science and Technology (KIST), Seoul, South Korea.
Center for Neuroscience, Korea Institute of Science and Technology (KIST); Convergence Research Center for Diagnosis, Treatment and Care System of Dementia; Division of Biomedical Science & Technology, KIST School, Korea University of Science and Technology, Seoul, South Korea.
Neural Regen Res. 2018 Jan;13(1):77-85. doi: 10.4103/1673-5374.224374.
A significant amount of evidence indicates that microRNAs (miRNAs) play an important role in drug addiction. The nucleus accumbens (NAc) is a critical part of the brain's reward circuit and is involved in a variety of psychiatric disorders, including depression, anxiety, and drug addiction. However, few studies have examined the expression of miRNAs and their functional roles in the NAc under conditions of morphine addiction. In this study, mice were intravenously infused with morphine (0.01, 0.03, 0.3, 1 and 3 mg/kg/infusion) and showed inverted U-shaped response. After morphine self-administration, NAc was used to analyze the functional networks of altered miRNAs and their putative target mRNAs in the NAc following intravenous self-administration of morphine. We utilized several bioinformatics tools, including Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway mapping and CyTargetLinker. We found that 62 miRNAs were altered and exhibited differential expression patterns. The putative targets were related to diverse regulatory functions, such as neurogenesis, neurodegeneration, and synaptic plasticity, as well as the pharmacological effects of morphine (receptor internalization/endocytosis). The present findings provide novel insights into the regulatory mechanisms of accumbal molecules under conditions of morphine addiction and identify several novel biomarkers associated with morphine addiction.
大量证据表明,微小RNA(miRNA)在药物成瘾中发挥着重要作用。伏隔核(NAc)是大脑奖赏回路的关键部分,与包括抑郁症、焦虑症和药物成瘾在内的多种精神疾病有关。然而,很少有研究探讨吗啡成瘾条件下NAc中miRNA的表达及其功能作用。在本研究中,给小鼠静脉注射吗啡(0.01、0.03、0.3、1和3mg/kg/次注射),小鼠呈现倒U形反应。在吗啡自我给药后,利用NAc分析静脉注射吗啡自我给药后NAc中miRNA及其假定靶mRNA的功能网络。我们使用了几种生物信息学工具,包括京都基因与基因组百科全书(KEGG)通路映射和CyTargetLinker。我们发现62种miRNA发生了改变并呈现出差异表达模式。假定的靶标与多种调节功能有关,如神经发生、神经退行性变和突触可塑性,以及吗啡的药理作用(受体内化/内吞作用)。本研究结果为吗啡成瘾条件下伏隔核分子的调节机制提供了新的见解,并鉴定了几种与吗啡成瘾相关的新型生物标志物。