Yerkes National Primate Research Center , Atlanta, GA , USA ; Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine , Atlanta, GA , USA.
Front Psychiatry. 2013 Jul 1;4:62. doi: 10.3389/fpsyt.2013.00062. eCollection 2013.
This review examines recent work on epigenetic mechanisms underlying animal models of fear learning as well as its translational implications in disorders of fear regulation, such as Post-traumatic Stress Disorder (PTSD). Specifically, we will examine work outlining roles of differential histone acetylation and DNA-methylation associated with consolidation, reconsolidation, and extinction in Pavlovian fear paradigms. We then focus on the numerous studies examining the epigenetic modifications of the Brain-derived neurotrophin factor (BDNF) pathway and the extension of these findings from animal models to recent work in human clinical populations. We will also review recently published data on FKBP5 regulation of glucocorticoid receptor function, and how this is modulated in animal models of PTSD and in human clinical populations via epigenetic mechanisms. As glucocorticoid regulation of memory consolidation is well established in fear models, we examine how these recent data contribute to our broader understanding of fear memory formation. The combined recent progress in epigenetic modulation of memory with the advances in fear neurobiology suggest that this area may be critical to progress in our understanding of fear-related disorders with implications for new approaches to treatment and prevention.
这篇综述考察了近期有关动物恐惧学习模型中表观遗传机制的研究,以及其在恐惧调节障碍(如创伤后应激障碍,PTSD)中的转化意义。具体来说,我们将探讨与巩固、再巩固和消退相关的组蛋白乙酰化和 DNA 甲基化差异的作用,这些作用在经典条件恐惧范式中得到了阐明。然后,我们将重点关注大量研究,这些研究检查了脑源性神经营养因子(BDNF)通路的表观遗传修饰,以及这些发现如何从动物模型扩展到人类临床人群中的最新研究。我们还将回顾最近关于 FKBP5 调节糖皮质激素受体功能的研究数据,以及 PTSD 动物模型和人类临床人群中如何通过表观遗传机制来调节这些发现。鉴于糖皮质激素对记忆巩固的调节在恐惧模型中已得到充分证实,我们将探讨这些最新数据如何有助于我们更全面地理解恐惧记忆的形成。记忆的表观遗传调节方面的最新进展与恐惧神经生物学方面的进展相结合,表明这一领域对于我们理解与恐惧相关的障碍至关重要,这对于治疗和预防这些障碍的新方法具有重要意义。