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伏隔核中 miR-124、Let-7d 和 miR-181a 的调节影响可卡因诱导的条件性位置偏爱表达、消退和复燃。

Regulation of MiR-124, Let-7d, and MiR-181a in the accumbens affects the expression, extinction, and reinstatement of cocaine-induced conditioned place preference.

机构信息

Division of Biochemistry, Department of Medicine, University of Fribourg, Fribourg, Switzerland.

出版信息

Neuropsychopharmacology. 2011 May;36(6):1149-64. doi: 10.1038/npp.2010.250. Epub 2011 Feb 9.

Abstract

Molecular adaptations underlying drug seeking and relapse remain largely unknown. Studies highlight post-transcriptional modifications mediated by microRNAs (miRNAs) in addiction and other neurological disorders. We have previously shown that chronic cocaine suppresses miR-124 and let-7d and induces the expression of miR-181a in mesolimbic pathway. To further address the role and target gene regulation network of these miRNAs in vivo in cocaine addiction, we developed lentiviral vector (LV)-expressing miRNAs and their corresponding silencers for stable and regulatable miRNA expression. We tested in vivo miRNA gain and loss of function on cocaine-induced conditioned place preference (CPP) by localized LV-miRNA regulation in the nucleus accumbens (NAc). LV-miR-124 and let-7d expression in the NAc attenuates cocaine CPP, whereas LV-miR-181a enhances it. Silencing miRNAs by corresponding LV-miRNA silencers expressing perfect miRNA target sequences inversed this effect on cocaine CPP. Doxycycline treatment for switching off silencer expression abolished the observed behavioral changes. Behavioral changes mediated by LV-miRNA regulation resulted in dynamic alterations in transcription factors, receptors, and other effector genes involved in cocaine-induced plasticity. Our results describe a complex regulatory pathway mediated by miRNAs in cocaine-mediated neuronal adaptations.

摘要

分子适应药物寻求和复发在很大程度上仍然未知。研究强调了 miRNA(miRNAs)在成瘾和其他神经障碍中的转录后修饰。我们之前已经表明,慢性可卡因抑制 miR-124 和 let-7d,并诱导中脑边缘通路中 miR-181a 的表达。为了进一步探讨这些 miRNA 在可卡因成瘾中的体内作用和靶基因调控网络,我们开发了表达 miRNA 及其相应抑制剂的慢病毒载体(LV),用于稳定和可调节的 miRNA 表达。我们通过在伏隔核(NAc)中局部 LV-miRNA 调节来测试体内 miRNA 功能增益和缺失对可卡因诱导的条件性位置偏爱(CPP)的影响。NAc 中的 LV-miR-124 和 let-7d 表达减弱了可卡因 CPP,而 LV-miR-181a 则增强了它。通过表达完美 miRNA 靶序列的相应 LV-miRNA 抑制剂沉默 miRNA,会使可卡因 CPP 产生相反的效果。用强力霉素治疗以关闭抑制剂表达会消除观察到的行为变化。LV-miRNA 调节介导的行为变化导致参与可卡因诱导可塑性的转录因子、受体和其他效应基因的动态改变。我们的研究结果描述了 miRNA 介导的可卡因介导的神经元适应中的一个复杂调控途径。

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