Canadian Centre for Behavioural Neuroscience, Department of Neuroscience, 4401 University Drive, Lethbridge, Alberta, Canada.
Department of Biology, University of Lethbridge, Lethbridge, AB T1K3M4 Canada.
Sci Rep. 2016 Nov 24;6:37814. doi: 10.1038/srep37814.
Ancestral stress can program stress sensitivity and health trajectories across multiple generations. While ancestral stress is uncontrollable to the filial generations, it is critical to identify therapies that overcome transgenerational programming. Here we report that prenatal stress in rats generates a transgenerationally heritable endocrine and epigenetic footprint and elevated stress sensitivity which can be alleviated by beneficial experiences in later life. Ancestral stress led to downregulated glucocorticoid receptor and prefrontal cortex neuronal densities along with precocious development of anxiety-like behaviours. Environmental enrichment (EE) during adolescence mitigated endocrine and neuronal markers of stress and improved miR-182 expression linked to brain-derived neurotrophic factor (BDNF) and neurotrophin-3 (NT-3) regulation in stressed lineages. Thus, EE may serve as a powerful intervention for adverse transgenerational programming through microRNA-mediated regulation of BDNF and NT-3 pathways. The identification of microRNAs that mediate the actions of EE highlights new therapeutic strategies for mental health conditions and psychiatric disease.
祖先压力可以在多代表现出压力敏感性和健康轨迹。虽然子孙后代无法控制祖先压力,但确定克服跨代编程的治疗方法至关重要。在这里,我们报告大鼠的产前压力会产生可遗传的内分泌和表观遗传痕迹,以及升高的压力敏感性,这种敏感性可以通过以后生活中的有益经历得到缓解。祖先压力导致糖皮质激素受体和前额叶皮层神经元密度降低,以及焦虑样行为的过早发展。青春期的环境丰富(EE)减轻了压力的内分泌和神经元标志物,并改善了与脑源性神经营养因子(BDNF)和神经营养因子-3(NT-3)调节相关的 miR-182 表达,从而减轻了压力谱系中的表达。因此,EE 可以通过 miRNA 介导的 BDNF 和 NT-3 通路调节作为一种强大的干预措施,用于治疗不利的跨代编程。鉴定介导 EE 作用的 microRNAs 突出了针对心理健康状况和精神疾病的新治疗策略。