Toffoli L V, Volpini V L, Nascimento L M, Silva W R, Verissimo L F, Estrada V B, Pelosi G G, Gomes M V
Research Centre on Health Sciences, University of Northern Parana (UNOPAR), Londrina, Parana, Brazil.
Centre of Biological Sciences, Department of Physiological Sciences, State University of Londrina (UEL), Londrina, Parana, Brazil.
Behav Brain Res. 2017 Jul 28;331:188-192. doi: 10.1016/j.bbr.2017.03.023. Epub 2017 Mar 22.
The potential of behavioral stress to affect epigenetic mechanisms of non-encephalic tissues is still underestimated. In the present study we evaluated the effects of chronic behavioral stress on the DNA methylation profile of rat lung cells. Furthermore, we evaluated the potential of physical exercise to modulate the changes evoked by behavioral stress in lung cells. Male Wistar rats were divided into four experimental groups: (1) animals submitted to chronic restraint stress (CRS) (ST group) during the period of the 67th-80th postnatal day (PND); (2) animals submitted to physical exercise (EX group) during the 53rd-79th PND; (3) animals submitted to swimming during the 53rd-79th PND and to CRS during the 67th-80th PND (EX-ST group); and (4) animals not submitted to stress or swimming protocols (CTL). Global DNA methylation was quantified using an ELISA-based approach and gene expression was evaluated by real time PCR. A decreased global DNA methylation profile was observed in the ST group, however physical exercise demonstrated protection of lung cells from this stress-related hypomethylation. Increased expression of the Dnmt1 gene was evidenced in the ST group, whereas physical exercise was shown to protect lung cells from this stress-related effect in the EX-ST group. Comparative analysis of the ST and EX groups revealed opposite effects on the expression of Dnmt3a and Dnmt3b; however, a stress-related increase in expression of Dnmt3a and Dnmt3b was not seen in the EX-ST group. Our data showed that behavioral stress induced significant changes in the DNA methylation profile of rat lung cells and that this could be modulated by physical exercise.
行为应激对非脑组织表观遗传机制的影响潜力仍被低估。在本研究中,我们评估了慢性行为应激对大鼠肺细胞DNA甲基化谱的影响。此外,我们还评估了体育锻炼调节行为应激在肺细胞中引发变化的潜力。雄性Wistar大鼠被分为四个实验组:(1) 在出生后第67 - 80天(PND)期间接受慢性束缚应激(CRS)的动物(ST组);(2) 在第53 - 79天PND期间进行体育锻炼的动物(EX组);(3) 在第53 - 79天PND期间游泳且在第67 - 80天PND期间接受CRS的动物(EX - ST组);以及(4) 未接受应激或游泳方案的动物(CTL组)。使用基于ELISA的方法对全局DNA甲基化进行定量,并通过实时PCR评估基因表达。在ST组中观察到全局DNA甲基化谱降低,然而体育锻炼显示出可保护肺细胞免受这种与应激相关的低甲基化影响。在ST组中证实Dnmt1基因表达增加,而在EX - ST组中体育锻炼显示出可保护肺细胞免受这种与应激相关的影响。ST组和EX组的比较分析揭示了对Dnmt3a和Dnmt3b表达的相反影响;然而,在EX - ST组中未观察到与应激相关的Dnmt3a和Dnmt3b表达增加。我们的数据表明,行为应激诱导大鼠肺细胞DNA甲基化谱发生显著变化,并且这种变化可通过体育锻炼进行调节。