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Expression levels of the BDNF gene and histone modifications around its promoters in the ventral tegmental area and locus ceruleus of rats during forced abstinence from morphine

机译:强制戒除吗啡期间大鼠腹侧被盖区和蓝斑中BDNF基因的表达水平及其启动子周围的组蛋白修饰

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Brain-derived neurotrophic factor (BDNF) plays a role in mediating molecular, cellular, and behavioral adaptations underlying drug addiction. Here, we examined the influence of withdrawal from repeated morphine treatment on the expression of BDNF mRNA in the ventral tegmental area (VTA) and locus coeruleus (LC) of the rat brain. We also studied whether alternations in mRNA levels of BDNF in these tissues are associated with histone modifications around promoters II and III of the BDNF gene. Thus, chromatin immunoprecipitation (CHIP) and quantitative (q)-PCR were employed to assess acetylation of histone H3 at K9/K14 and trimethylation of histone H3 at K9. Results of qRT-PCR showed that levels of BDNF mRNA in both VTA and LC were significantly increased 7 days rather than 2 h or 24 h following the last injection of morphine. Consistently, CHIP and qPCR analysis revealed that on day 7 of morphine abstinence, both VTA and LC levels of histone methylation at BDNF promoters II and III of morphine treated rats were significantly lower than control animals. Morphine withdrawal caused only a significant increase in H3 acetylation at the promoter II in the LC. These data demonstrate the involvement of histone H3 methylation in the regulation of gene expression in the VTA and LC of rats during forced abstinence of morphine.
机译:脑源性神经营养因子(BDNF)在介导潜在的药物成瘾的分子,细胞和行为适应中起作用。在这里,我们检查了重复吗啡治疗退出对大鼠脑腹侧被盖区(VTA)和蓝斑轨迹(LC)中BDNF mRNA表达的影响。我们还研究了这些组织中BDNF mRNA水平的变化是否与BDNF基因启动子II和III周围的组蛋白修饰有关。因此,染色质免疫沉淀(CHIP)和定量(q)-PCR用于评估K9 / K14处组蛋白H3的乙酰化和K9处组蛋白H3的三甲基化。 qRT-PCR的结果表明,VTA和LC中BDNF mRNA的水平显着增加了7天,而不是最后一次注射吗啡后2小时或24小时。一致地,CHIP和qPCR分析显示,在吗啡戒断的第7天,吗啡治疗大鼠的BDNF启动子II和III的组蛋白甲基化的VTA和LC水平均显着低于对照动物。吗啡戒断仅引起LC启动子II处H3乙酰化的显着增加。这些数据证明在强制戒断吗啡期间,组蛋白H3甲基化参与了大鼠VTA和LC中基因表达的调节。

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