慢性社会隔离应激对性别特异性影响的神经回路和活动动力学。
Neural circuits and activity dynamics underlying sex-specific effects of chronic social isolation stress.
机构信息
Department of Physiology and Biophysics, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA.
Department of Physiology and Biophysics, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA; School of Biomedical Engineering and Technology, Tianjin Medical University, Tianjin 300070, China.
出版信息
Cell Rep. 2021 Mar 23;34(12):108874. doi: 10.1016/j.celrep.2021.108874.
Exposure to prolonged stress in critical developmental periods induces heightened vulnerability to psychiatric disorders, which may have sex-specific consequences. Here we investigate the neuronal circuits mediating behavioral changes in mice after chronic adolescent social isolation stress. Escalated aggression is exhibited in stressed males, while social withdrawal is shown in stressed females. In vivo multichannel recordings of free-moving animals indicate that pyramidal neurons in prefrontal cortex (PFC) from stressed males exhibit the significantly decreased spike activity during aggressive attacks, while PFC pyramidal neurons from stressed females show a blunted increase of discharge rates during sociability tests. Chemogenetic and electrophysiological evidence shows that PFC hypofunctioning and BLA principal neuron hyperactivity contribute to the elevated aggression in stressed males, while PFC hypofunctioning and VTA dopamine neuron hypoactivity contribute to the diminished sociability in stressed females. These results establish a framework for understanding the circuit and physiological mechanisms underlying sex-specific divergent effects of stress.
在关键发育阶段长期暴露于压力会导致对精神疾病的易感性增加,这可能具有性别特异性的后果。在这里,我们研究了慢性青春期社交隔离应激后小鼠行为变化的神经元回路。应激雄性表现出攻击性增强,而应激雌性则表现出社交回避。在自由活动动物的体内多通道记录中,应激雄性前额叶皮层(PFC)中的锥体神经元在攻击性行为期间表现出明显减少的放电活动,而应激雌性 PFC 锥体神经元在社交性测试期间显示放电率的钝性增加。化学遗传和电生理证据表明,PFC 功能低下和 BLA 主神经元过度活跃导致应激雄性攻击性增强,而 PFC 功能低下和 VTA 多巴胺神经元活性降低导致应激雌性社交性降低。这些结果为理解应激对雄性和雌性产生性别特异性不同影响的回路和生理机制奠定了框架。