Canadian Centre for Behavioural Neuroscience, Department of Neuroscience, University of Lethbridge, 4401 University Drive, Lethbridge, Alberta, T1K 3M4, Canada.
Department of Biological Sciences, University of Lethbridge, Lethbridge, Alberta, T1K 3M4, Canada.
Sci Rep. 2019 Apr 23;9(1):6389. doi: 10.1038/s41598-019-42691-z.
Experiences during early development are powerful determinants of lifetime mental health. Here we investigated if ancestral stress regulates the brain's epigenetic memory to alter neuromorphology and emotionality in the remote F4 progeny. Pregnant female rat dams of the parental F0 generation were exposed to stress on gestational days 12-18. To generate a transgenerational stress lineage, their pregnant daughters (F1), grand-daughters (F2) and great-grand-daughters (F3) remained undisturbed. To generate a multigenerational stress lineage, pregnant dams of each generation (F1-F3) were stressed. A lineage of non-stress controls (F0-F3) was also produced. Multigenerational stress exceeded the impact of transgenerational stress by increasing anxiety-like behaviours and stress response in young and middle-aged F4 males but not females. Functional changes were accompanied by reduced spine density in the male medial prefrontal cortex with opposite effects in the orbital frontal cortex. Ancestral stress regulated cortical miR-221 and miR-26 expression and their target genes, thus downregulating ntrk2 and map1a genes in males while downregulating crh and upregulating map1a genes in females. These miRNA-dependent pathways are candidates for developmental programming of lifetime mental health. Thus, multigenerational stress in particular determines sexually dimorphic predisposition to stress vulnerability and generates a phenotype resembling symptoms of post-traumatic stress disorder.
早期经历是决定终身心理健康的重要因素。在这里,我们研究了祖先应激是否调节大脑的表观遗传记忆,以改变远程 F4 后代的神经形态和情绪。在 F0 代的孕鼠母体中,在妊娠第 12-18 天进行应激处理。为了产生跨代应激谱系,它们的孕鼠女儿(F1)、孙女(F2)和曾孙女(F3)保持不受干扰。为了产生多代应激谱系,每一代(F1-F3)的孕鼠都受到应激处理。还产生了非应激对照(F0-F3)谱系。多代应激通过增加年轻和中年 F4 雄性的焦虑样行为和应激反应,超过了跨代应激的影响,但对雌性没有影响。功能变化伴随着雄性内侧前额皮质的棘密度减少,而眶额皮质则有相反的影响。祖先应激调节皮质 miR-221 和 miR-26 的表达及其靶基因,从而下调雄性中的 ntrk2 和 map1a 基因,同时下调雌性中的 crh 并上调 map1a 基因。这些 miRNA 依赖性途径是决定终身心理健康的发育编程的候选途径。因此,特别是多代应激决定了对压力易感性的性别二态倾向,并产生了类似于创伤后应激障碍症状的表型。