Tyler Christina R Steadman, Smoake Jane J W, Solomon Elizabeth R, Villicana Estrella, Caldwell Kevin K, Allan Andrea M
Bioenergy and Biome Sciences, Los Alamos National Laboratory, Los Alamos, NM, United States.
Department of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, United States.
Front Genet. 2018 Jun 15;9:200. doi: 10.3389/fgene.2018.00200. eCollection 2018.
Several studies have demonstrated that exposure to arsenic in drinking water adversely affects brain development and cognitive function in adulthood. While the mechanism by which arsenic induces adverse neurological outcomes remains elusive, studies suggest a link between reduced levels of histone acetylation and impaired performance on a variety of behavioral tasks following arsenic exposure. Using our developmental arsenic exposure (DAE) paradigm, we have previously reported reduced histone acetylation and associated histone acetyltransferase enzyme expression in the frontal cortex of C57BL/6J adult male mice, with no changes observed in the female frontal cortex. In the present study, we sought to determine if DAE produced sex-dependent deficits in frontal cortical executive function using the Y-maze acquisition and reversal learning tasks, which are specific for assessing cognitive flexibility. Further, we tested whether the administration of valproic acid, a class I-IIa histone deacetylase inhibitor, was able to mitigate behavioral and biochemical changes resulting from DAE. As anticipated, DAE inhibited acquisition and reversal learning performance in adult male, but not female, mice. Valproate treatment for 2 weeks restored reversal performance in the male arsenic-exposed offspring, while not affecting female performance. Protein levels of HDACs 1, 2, and 5 were elevated following behavioral assessment but only in DAE male mice; restoration of appropriate HDAC levels occurred after valproate treatment and was concurrent with improved behavioral performance, particularly during reversal learning. Female frontal cortical levels of HDAC enzymes were not impacted by DAE or valproate treatment. Finally, mRNA expression levels of brain-derived neurotrophic factor, Bdnf, which has been implicated in the control of frontal cortical flexibility and is regulated by HDAC5, were elevated in DAE male mice and restored to normal levels following HDACi treatment. Levels of mRNA encoding glutamate receptor ionotropic NMDA type subunits, which have been linked to cognitive flexibility, were not related to the reversal learning deficit in the DAE mice and were not altered by HDACi treatments. These findings demonstrate that DAE alters frontal cortical HDAC levels and Bdnf expression in males, but not females, and that these molecular changes are associated with sex-dependent differences in cognitive flexibility in a reversal-learning task.
多项研究表明,饮用水中砷的暴露会对成年期的大脑发育和认知功能产生不利影响。虽然砷诱导不良神经学后果的机制仍不清楚,但研究表明,砷暴露后组蛋白乙酰化水平降低与各种行为任务表现受损之间存在联系。使用我们的发育性砷暴露(DAE)模型,我们之前报道过,C57BL/6J成年雄性小鼠额叶皮质中的组蛋白乙酰化及相关组蛋白乙酰转移酶表达降低,而雌性额叶皮质未观察到变化。在本研究中,我们试图通过Y迷宫获取和逆向学习任务来确定DAE是否会在额叶皮质执行功能方面产生性别依赖性缺陷,这些任务专门用于评估认知灵活性。此外,我们测试了I-IIa类组蛋白脱乙酰酶抑制剂丙戊酸的给药是否能够减轻DAE导致的行为和生化变化。正如预期的那样,DAE抑制了成年雄性小鼠(而非雌性小鼠)的获取和逆向学习表现。丙戊酸盐治疗2周恢复了砷暴露雄性后代的逆向学习表现,而未影响雌性的表现。行为评估后,HDACs 1、2和5的蛋白水平升高,但仅在DAE雄性小鼠中出现;丙戊酸盐治疗后HDAC水平恢复正常,并与行为表现改善同时出现,特别是在逆向学习期间。雌性额叶皮质中HDAC酶的水平不受DAE或丙戊酸盐治疗的影响。最后,在DAE雄性小鼠中,与额叶皮质灵活性控制相关且受HDAC5调节的脑源性神经营养因子Bdnf的mRNA表达水平升高,HDACi治疗后恢复到正常水平。编码与认知灵活性相关的离子型NMDA型谷氨酸受体亚基的mRNA水平与DAE小鼠的逆向学习缺陷无关,且未因HDACi治疗而改变。这些发现表明,DAE改变了雄性而非雌性的额叶皮质HDAC水平和Bdnf表达,并且这些分子变化与逆向学习任务中认知灵活性的性别依赖性差异相关。