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Expression Levels of the Tyrosine Hydroxylase Gene and Histone Modifications Around its Promoter in the Locus Coeruleus and Ventral Tegmental Area of Rats during Forced Abstinence from Morphine

机译:酪氨酸羟化酶基因的表达水平及其启动子局部促进剂的促进剂和腹侧大鼠腹部腹膜腹部的促进剂

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Background: Epigenetic mechanisms such as histone modifications may be involved in the structural and behavioral changes associated with addiction. We studied whether morphine-induced changes in mRNA levels of the catecholamine biosynthesis enzyme, tyrosine hydroxylase (TH), are associated with histone modifications around the promoter of this gene in the locus coeruleus (LC) and ventral tegmental area (VTA) of rats. Methods: Dependence was induced in rats by intraperitoneal injections of morphine for 11 days. The animals were killed 2 h (chronic morphine), 24 h and 7 days (spontaneous withdrawal) after the last injection of morphine. Results: Analysis of our real-time quantitative reverse transcription PCR results by 1-way ANOVA showed significant upregulation (5.13 +/- 0.39 folds) of LC levels of the TH transcript 24 h after the last injection of morphine to rats, when compared with 2 h and 7 days time points. Chronic morphine and morphine abstinence failed to cause any significant changes in the levels of TH mRNA in the VTA after cessation of morphine. Consistently, chromatin immunoprecipitation real-time quantitative PCR assays revealed that 24 h after the last injection of morphine, levels of H3 acetylation were significantly increased (4.12 +/- 0.38 folds) at the promoter of the TH gene in the LC but not in the VTA. Our data also showed that histone H3 trimethylation failed to change around the TH gene promoter either in the VTA or in the LC after morphine abstinence. Conclusions: Results of the present study, for the first time, demonstrate the involvement of histone H3 acetylation in the regulation of TH gene expression in the LC of rats during forced abstinence from morphine. (C) 2018 S. Karger AG, Basel
机译:背景:诸如组蛋白修饰的表观遗传机制可以参与与成瘾相关的结构和行为变化。我们研究了吗啡诱导的吗啡素生物合成酶的mRNA水平的变化,酪氨酸羟化酶(TH)与局部基因库(LC)和大鼠腹侧腹部区域(VTA)的该基因的启动子周围的组蛋白修饰相关。方法:通过腹膜内注射吗啡在大鼠中诱导依赖性11天。在最后一次注射吗啡后,动物被杀死2小时(慢性吗啡),24小时和7天(自发戒断)。结果:通过单向ANOVA进行实时定量逆转录PCR的实时定量逆转录PCR结果表明,在最后一次注射吗啡的情况后,TH转录的LC水平的显着上调(5.13 +/- 0.39倍)。 2小时和7天的时间点。慢性吗啡和吗啡禁因未能在随访后导致vTA在vta中的任何显着变化。始终如一地,染色质免疫沉淀实时定量PCR测定显示,在最后一次注射吗啡后24小时,在LC的TH基因的启动子上显着增加(4.12 +/- 0.38倍)的水平,但不在VTA。我们的数据还表明,组蛋白H3三甲基化未能在vTA或吗啡禁止后在VTA或LC中围绕该基因启动剂改变。结论:本研究的结果首次证明了组蛋白H3乙酰化在转霉戒断中大鼠LC的调节中的调节中的调控。 (c)2018年S. Karger AG,巴塞尔

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