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母婴分离与成年大鼠的DNA甲基化及行为变化有关。

Maternal separation is associated with DNA methylation and behavioural changes in adult rats.

作者信息

Anier Kaili, Malinovskaja Kristina, Pruus Katrin, Aonurm-Helm Anu, Zharkovsky Alexander, Kalda Anti

机构信息

Department of Pharmacology, Institute of Bio- and Translational Medicine, University of Tartu, 19 Ravila street, Tartu 50411, Estonia.

Department of Pharmacology, Institute of Bio- and Translational Medicine, University of Tartu, 19 Ravila street, Tartu 50411, Estonia.

出版信息

Eur Neuropsychopharmacol. 2014 Mar;24(3):459-68. doi: 10.1016/j.euroneuro.2013.07.012. Epub 2013 Aug 6.

Abstract

Early life stress is known to promote long-term neurobiological changes, which may underlie the increased risk of psychopathology. Maternal separation (MS) is used as an early life stressor that causes profound neurochemical and behavioural changes in the pups that persist into adulthood. However, the exact mechanism of how MS alters these behavioural changes is not yet understood. Epigenetic modifications, such as DNA methylation, are critical regulators of persistent gene expression changes and may be related to behavioural disorders. The aim of the present study was to investigate whether early life stress on rats could alter cocaine-induced behavioural sensitisation in adulthood via aberrant DNA methylation. We have three main findings: (1) MS increased DNA methyltransferases (DNMTs) expression in the nucleus accumbens (NAc) of infant and adult rats; (2) MS induced DNA hypomethylation on a global level in the NAc, and hypermethylation of the promoter regions of the protein phosphatase 1 catalytic subunit (PP1C) and adenosine A2Areceptor (A2AR) genes, which was associated with their transcriptional downregulation in the NAc; (3) MS-induced molecular changes paralleled an increased response to cocaine-induced locomotor activity and exploratory behaviour in adult rats. Thus, our results suggest that stressful experiences in early life may create a background, via aberrant DNA methylation, which promotes the development of cocaine-induced behavioural sensitisation in adulthood.

摘要

已知早期生活应激会促进长期的神经生物学变化,这可能是精神病理学风险增加的潜在原因。母婴分离(MS)被用作一种早期生活应激源,它会导致幼崽出现深刻的神经化学和行为变化,并持续到成年期。然而,MS如何改变这些行为变化的确切机制尚不清楚。表观遗传修饰,如DNA甲基化,是持续基因表达变化的关键调节因子,可能与行为障碍有关。本研究的目的是调查大鼠早期生活应激是否会通过异常的DNA甲基化改变成年期可卡因诱导的行为敏化。我们有三个主要发现:(1)MS增加了幼鼠和成年大鼠伏隔核(NAc)中DNA甲基转移酶(DNMTs)的表达;(2)MS在NAc中诱导了整体水平的DNA低甲基化,以及蛋白磷酸酶1催化亚基(PP1C)和腺苷A2A受体(A2AR)基因启动子区域的高甲基化,这与其在NAc中的转录下调有关;(3)MS诱导的分子变化与成年大鼠对可卡因诱导的运动活动和探索行为的反应增加平行。因此,我们的结果表明,早期生活中的应激经历可能通过异常的DNA甲基化创造一种背景,促进成年期可卡因诱导的行为敏化的发展。

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