Dayer Alexandre
Departments of Mental Health and Psychiatry and Basic Neurosciences, University of Geneva Medical School, Geneva, Switzerland.
Dialogues Clin Neurosci. 2014 Mar;16(1):29-41. doi: 10.31887/DCNS.2014.16.1/adayer.
Risk for adult psychiatric disorders is partially determined by early-life alterations occurring during neural circuit formation and maturation. In this perspective, recent data show that the serotonin system regulates key cellular processes involved in the construction of cortical circuits. Translational data for rodents indicate that early-life serotonin dysregulation leads to a wide range of behavioral alterations, ranging from stress-related phenotypes to social deficits. Studies in humans have revealed that serotonin-related genetic variants interact with early-life stress to regulate stress-induced cortisol responsiveness and activate the neural circuits involved in mood and anxiety disorders. Emerging data demonstrate that early-life adversity induces epigenetic modifications in serotonin-related genes. Finally, recent findings reveal that selective serotonin reuptake inhibitors can reinstate juvenile-like forms of neural plasticity, thus allowing the erasure of long-lasting fear memories. These approaches are providing new insights on the biological mechanisms and clinical application of antidepressants.
成人精神疾病的风险部分由神经回路形成和成熟过程中发生的早期生命改变所决定。从这个角度来看,最近的数据表明,血清素系统调节参与皮质回路构建的关键细胞过程。啮齿动物的转化数据表明,早期生命中的血清素失调会导致广泛的行为改变,从与压力相关的表型到社交缺陷。对人类的研究表明,与血清素相关的基因变异与早期生命压力相互作用,以调节压力诱导的皮质醇反应性,并激活参与情绪和焦虑障碍的神经回路。新出现的数据表明,早期生命逆境会诱导血清素相关基因的表观遗传修饰。最后,最近的研究结果表明,选择性血清素再摄取抑制剂可以恢复类似幼年的神经可塑性形式,从而消除长期的恐惧记忆。这些方法为抗抑郁药的生物学机制和临床应用提供了新的见解。