Biological Psychiatry Unit, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Via Pilastroni 4, 25125, Brescia, Italy.
Stress, Psychiatry and Immunology Laboratory, Department of Psychological Medicine, Institute of Psychiatry, King's College London, Coldharbour Lane, London, SE5 9NU, UK.
J Neural Transm (Vienna). 2019 Sep;126(9):1241-1258. doi: 10.1007/s00702-019-02048-2. Epub 2019 Jul 26.
The exposure to stressful experiences during the prenatal period and through the first years of life is known to affect the brain developmental trajectories, leading to an enhanced vulnerability for the development of several psychiatric disorders later in life. However, not all the subjects exposed to the same stressful experience develop a pathologic condition, as some of them, activating coping strategies, become more resilient. The disclosure of mechanisms associated with stress vulnerability or resilience may allow the identification of novel biological processes and potential molecules that, if properly targeted, may prevent susceptibility or potentiate resilience. Over the last years, miRNAs have been proposed as one of the epigenetic mechanisms mediating the long-lasting effects of stress. Accordingly, they are associated with the development of stress vulnerability or resilience-related strategies. Moreover, miRNAs have been proposed as possible biomarkers able to identify subjects at high risk to develop depression and to predict the response to pharmacological treatments. In this review, we aimed to provide an overview of findings from studies in rodents and humans focused on the involvement of miRNAs in the mechanisms of stress response with the final goal to identify distinct sets of miRNAs involved in stress vulnerability or resilience. In addition, we reviewed studies on alterations of miRNAs in the context of depression, showing data on the involvement of miRNAs in the pathogenesis of the disease and in the efficacy of pharmacological treatments, discussing the potential utility of miRNAs as peripheral biomarkers able to predict the treatment response.
在产前和生命早期经历应激体验已知会影响大脑发育轨迹,导致日后发生多种精神障碍的易感性增加。然而,并非所有经历相同应激体验的人都会出现病理状况,因为有些人会激活应对策略,从而变得更有韧性。揭示与应激易感性或韧性相关的机制,可以发现新的生物学过程和潜在的分子,如果靶向这些分子,可能会预防易感性或增强韧性。近年来,miRNAs 被提出作为介导应激的长期影响的表观遗传机制之一。因此,它们与应激易感性或韧性相关策略的发展有关。此外,miRNAs 被提出作为可能的生物标志物,能够识别有发展为抑郁症风险的个体,并预测对药物治疗的反应。在这篇综述中,我们旨在提供啮齿动物和人类研究中关于 miRNAs 参与应激反应机制的研究结果的概述,最终目的是确定参与应激易感性或韧性的不同 miRNA 集。此外,我们还回顾了关于 miRNAs 在抑郁症背景下改变的研究,展示了 miRNAs 参与疾病发病机制和药物治疗效果的数据,讨论了 miRNAs 作为能够预测治疗反应的外周生物标志物的潜在效用。