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应激游泳导致染色质改变,从而引起前强啡肽原转录增加。

Chromatin alterations in response to forced swimming underlie increased prodynorphin transcription.

机构信息

The Laboratory of the Biology of Addictive Diseases, The Rockefeller University, New York, NY 10065, USA.

出版信息

Neuroscience. 2012 Sep 18;220:109-18. doi: 10.1016/j.neuroscience.2012.06.006. Epub 2012 Jun 12.

Abstract

Antagonism of the kappa opioid receptor (KOR) has been reported to have anti-depressant-like properties. The dynorphin/KOR system is a crucial neurochemical substrate underlying the pathologies of addictive diseases, affective disorders and other disease states. However, the molecular underpinnings and neuroanatomical localization of the dysregulation of this system have not yet been fully elucidated. Utilizing the Porsolt Forced Swim Test (FST), an acute stressor commonly used as in rodent models measuring antidepressant efficacy, male Sprague-Dawley rats were subject to forced swimming for 15 min, treated 1h with vehicle or norbinaltorphimine (nor-BNI) (5 or 10mg/kg), and then 1 day later subject to FST for 5 min. In accordance with previous findings, nor-BNI dose dependently increased climbing time and reduced immobility. In comparison to control animals not exposed to FST, we observed a significant elevation in prodynorphin (pDyn) mRNA levels following FST using real-time optical polymerase chain reaction (PCR) in the caudate putamen but not in the nucleus accumbens, hypothalamus, amygdala, frontal cortex, or hippocampus. nor-BNI treatment did not affect pDyn mRNA levels in comparison to animals that received vehicle. The corresponding brain regions from the opposite hemisphere were analyzed for underlying chromatin modifications of the prodynorphin gene promoter region using chromatin immunoprecipitation with antibodies against specifically methylated histones H3K27Me2, H3K27Me3, H3K4Me2, and H3K4Me3, as well as CREB-1 and MeCP2. Significant alterations in proteins bound to DNA in the Cre-3, Cre-4, and Sp1 regions of the prodynorphin promoter were found in the caudate putamen of the FST saline-treated animals compared to control animals, with no changes observed in the hippocampus. Epigenetic changes resulting in elevated dynorphin levels specifically in the caudate putamen may in part underlie the enduring effects of stress.

摘要

κ 阿片受体(KOR)拮抗剂具有抗抑郁样作用。内啡肽/KOR 系统是成瘾性疾病、情感障碍和其他疾病状态的病理生理学的关键神经化学基础。然而,该系统失调的分子基础和神经解剖学定位尚未完全阐明。利用强迫游泳试验(FST),一种常用于测量抗抑郁疗效的啮齿动物模型中的急性应激源,雄性 Sprague-Dawley 大鼠被强迫游泳 15 分钟,用载体或 norbinaltorphimine(nor-BNI)(5 或 10mg/kg)处理 1 小时,然后在 1 天后进行 FST 5 分钟。与未暴露于 FST 的对照动物相比,我们使用实时光学聚合酶链反应(PCR)观察到在尾壳核中,而不是在伏隔核、下丘脑、杏仁核、前额皮质或海马体中,FST 后 prodynorphin(pDyn)mRNA 水平显著升高。与接受载体的动物相比,nor-BNI 处理并未影响 pDyn mRNA 水平。用针对特异性甲基化组蛋白 H3K27Me2、H3K27Me3、H3K4Me2 和 H3K4Me3 以及 CREB-1 和 MeCP2 的抗体进行染色质免疫沉淀,分析相反半球的相应脑区,以研究 prodynorphin 基因启动子区域的染色质修饰。与对照动物相比,在 FST 盐水处理的动物的尾壳核中发现 prodynorphin 启动子的 Cre-3、Cre-4 和 Sp1 区域与 DNA 结合的蛋白质发生了显著变化,而在海马体中则没有观察到变化。在尾壳核中特定 dynorphin 水平升高的表观遗传变化可能部分是应激的持久影响的基础。

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