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Temporally specific miRNA miRNA expression patterns in the dorsal and ventral striatum of addiction‐prone rats

机译:逐步特异性miRNA miRNA表达模式,易于大鼠的背部和腹侧纹状体

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Abstract 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.
机译:腹侧和背纹体内的摘要MicroRNAS(miRNA)已显示调节瘾相关行为。但是,目前尚不清楚可卡因的体验是如何改变纹纹亚区域内成瘾相关miRNA的表达。此外,尚不知道纹状体中miRNA的差异表达是否有助于上瘾脆弱性的个体差异。我们首先检查了可卡因自我给药对细胞核核心核心核心和核心腺壳(NACSH)的miR-101b,miR-137,miR-212和miR-132表达的影响,以及背侧纹状体和背侧纹状体( DLS)。然后,我们在被确定为“成瘾”的动物的纹状体次区域中,在自我管理培训或灭绝后立即进行了灭绝和复发测试,检查了这些相同的miRNA的表达。可卡因自我管理与在纹状体内以区域离散方式的miRNA表达的变化有关,并且在核心核心中发生的最明显的变化。当我们检测自我管理后的成瘾易一只大鼠的miRNA谱时,我们观察了背部纹状体中的miR-212水平增加。消失和复发测试后,易患大鼠在NACSH中的miR-101b,miR-137,miR-212和miR-132中的表达显着增加,并且在DLS中的miR-137。该研究识别与在成瘾周期的过程中不同的纹状体子区域的接合一致的miRNA表达中的时间特异性变化。在成瘾循环后期的NACSH和DLS中miRNA表达的增加可能提高了习惯性药物,因此可能有助于鉴定旨在治疗成瘾的目标。

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