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调节中前额叶多巴胺电路介导了生命早期应激引起的前额叶皮层突触失衡。

Dysregulation of the mesoprefrontal dopamine circuit mediates an early-life stress-induced synaptic imbalance in the prefrontal cortex.

机构信息

Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA; Department of Pharmacology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA.

Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.

出版信息

Cell Rep. 2021 May 4;35(5):109074. doi: 10.1016/j.celrep.2021.109074.

Abstract

Stress adversely affects an array of cognitive functions. Although stress-related disorders are often addressed in adulthood, far less is known about how early-life stress (ELS) affects the developing brain in early postnatal periods. Here we show that ELS, induced by maternal separation, leads to synaptic alteration of layer 2/3 pyramidal neurons in the prefrontal cortex (PFC) of mice. We find that layer 2/3 neurons show increased excitatory synapse numbers following ELS and that this is accompanied by hyperexcitability of PFC-projecting dopamine (DA) neurons in the ventral tegmental area. Notably, excitatory synaptic change requires local signaling through DA D2 receptors. In vivo pharmacological treatment with a D2 receptor agonist in the PFC of control mice mimics the effects of ELS on synaptic alterations. Our findings reveal a neuromodulatory mechanism underlying ELS-induced PFC dysfunction, and this mechanism may facilitate a more comprehensive understanding of how ELS leads to mental disorders.

摘要

压力会对一系列认知功能产生不良影响。尽管与压力相关的疾病通常在成年期得到解决,但人们对早期生活压力 (ELS) 如何在出生后早期影响发育中的大脑知之甚少。在这里,我们表明,由母体分离引起的 ELS 会导致前额叶皮层 (PFC) 中 2/3 层锥体神经元的突触改变。我们发现,ELS 后 2/3 层神经元的兴奋性突触数量增加,并且伴随着腹侧被盖区中投射到 PFC 的多巴胺 (DA) 神经元的过度兴奋。值得注意的是,兴奋性突触变化需要通过 DA D2 受体进行局部信号转导。在控制小鼠的 PFC 中进行体内药理学治疗,用 D2 受体激动剂模拟 ELS 对突触改变的影响。我们的研究结果揭示了 ELS 诱导的 PFC 功能障碍的神经调节机制,这一机制可能有助于更全面地了解 ELS 如何导致精神障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98bb/8138943/5814fafdfd7d/nihms-1700571-f0002.jpg

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