Neurobiology of Addiction Laboratory, School of Biomedical Sciences and Pharmacy and the Centre for Translational Neuroscience and Mental Health Research, University of Newcastle and the Hunter Medical Research Institute, Australia.
Brain Health Institute, Rutgers University, USA.
Addict Biol. 2018 Mar;23(2):631-642. doi: 10.1111/adb.12520. Epub 2017 Jun 13.
MicroRNAs (miRNAs) within the ventral and dorsal striatum have been shown to regulate addiction-relevant behaviours. However, it is unclear how cocaine experience alone can alter the expression of addiction-relevant miRNAs within striatal subregions. Further, it is not known whether differential expression of miRNAs in the striatum contributes to individual differences in addiction vulnerability. We first examined the effect of cocaine self-administration on the expression of miR-101b, miR-137, miR-212 and miR-132 in nucleus accumbens core and nucleus accumbens shell (NAcSh), as well as dorsomedial striatum and dorsolateral striatum (DLS). We then examined the expression of these same miRNAs in striatal subregions of animals identified as being 'addiction-prone', either immediately following self-administration training or following extinction and relapse testing. Cocaine self-administration was associated with changes in miRNA expression in a regionally discrete manner within the striatum, with the most marked changes occurring in the nucleus accumbens core. When we examined the miRNA profile of addiction-prone rats following self-administration, we observed increased levels of miR-212 in the dorsomedial striatum. After extinction and relapse testing, addiction-prone rats showed significant increases in the expression of miR-101b, miR-137, miR-212 and miR-132 in NAcSh, and miR-137 in the DLS. This study identifies temporally specific changes in miRNA expression consistent with the engagement of distinct striatal subregions across the course of the addiction cycle. Increased dysregulation of miRNA expression in NAcSh and DLS at late stages of the addiction cycle may underlie habitual drug seeking, and may therefore aid in the identification of targets designed to treat addiction.
腹侧纹状体和背侧纹状体中的 microRNAs(miRNAs)已被证明可调节与成瘾相关的行为。然而,尚不清楚可卡因体验本身如何改变纹状体亚区中与成瘾相关的 miRNAs 的表达。此外,尚不清楚纹状体中 miRNAs 的差异表达是否有助于个体对成瘾易感性的差异。我们首先研究了可卡因自我给药对伏隔核核心和伏隔核壳(NAcSh)以及背侧纹状体和背外侧纹状体(DLS)中 miR-101b、miR-137、miR-212 和 miR-132 表达的影响。然后,我们研究了在自我给药训练后或在消退和复发测试后被鉴定为“易成瘾”的动物的纹状体内这些相同 miRNAs 的表达。可卡因自我给药与纹状体中区域离散方式的 miRNA 表达变化有关,其中最明显的变化发生在伏隔核核心。当我们研究自我给药后易成瘾大鼠的 miRNA 谱时,我们观察到背侧纹状体中 miR-212 的水平升高。在消退和复发测试后,易成瘾大鼠在 NAcSh 中显示 miR-101b、miR-137、miR-212 和 miR-132 的表达显著增加,在 DLS 中 miR-137 的表达增加。这项研究确定了 miRNA 表达的时间特异性变化,与成瘾周期过程中不同纹状体亚区的参与一致。在成瘾周期的后期,miRNA 表达的失调增加可能是习惯性药物寻求的基础,因此可能有助于识别旨在治疗成瘾的靶点。