Laboratory of Behavioral and Genomic Neuroscience, NIAAA, Bethesda, MD, USA.
Neuropsychopharmacology. 2012 May;37(6):1534-47. doi: 10.1038/npp.2011.340. Epub 2012 Feb 15.
Mood and anxiety disorders develop in some but not all individuals following exposure to stress and psychological trauma. However, the factors underlying individual differences in risk and resilience for these disorders, including genetic variation, remain to be determined. Isogenic inbred mouse strains provide a valuable approach to elucidating these factors. Here, we performed a comprehensive examination of the extinction-impaired 129S1/SvImJ (S1) inbred mouse strain for multiple behavioral, autonomic, neuroendocrine, and corticolimbic neuronal morphology phenotypes. We found that S1 exhibited fear overgeneralization to ambiguous contexts and cues, impaired context extinction and impaired safety learning, relative to the (good-extinguishing) C57BL/6J (B6) strain. Fear overgeneralization and impaired extinction was rescued by treatment with the front-line anxiety medication fluoxetine. Telemetric measurement of electrocardiogram signals demonstrated autonomic disturbances in S1 including poor recovery of fear-induced suppression of heart rate variability. S1 with a history of chronic restraint stress displayed an attenuated corticosterone (CORT) response to a novel, swim stressor. Conversely, previously stress-naive S1 showed exaggerated CORT responses to acute restraint stress or extinction training, insensitivity to dexamethasone challenge, and reduced hippocampal CA3 glucocorticoid receptor mRNA, suggesting downregulation of negative feedback control of the hypothalamic-pituitary-adrenal axis. Analysis of neuronal morphology in key neural nodes within the fear and extinction circuit revealed enlarged dendritic arbors in basolateral amygdala neurons in S1, but normal infralimbic cortex and prelimbic cortex dendritic arborization. Collectively, these data provide convergent support for the utility of the S1 strain as a tractable model for elucidating the neural, molecular and genetic basis of persistent, excessive fear.
情绪和焦虑障碍在一些人而非所有人中发展,这些人在经历压力和心理创伤后会出现这种情况。然而,导致这些障碍风险和弹性个体差异的因素,包括遗传变异,仍有待确定。同基因近交系小鼠品系为阐明这些因素提供了一种有价值的方法。在这里,我们对 129S1/SvImJ(S1)近交系小鼠进行了全面研究,以研究其多种行为、自主、神经内分泌和皮质边缘神经元形态表型。我们发现,与(良好消除)C57BL/6J(B6)品系相比,S1 表现出对模糊情境和线索的恐惧泛化过度、情境消除和安全学习受损。氟西汀(一线焦虑药物)的治疗挽救了 S1 的恐惧泛化过度和消除受损。心电图信号的遥测测量表明 S1 存在自主神经紊乱,包括恐惧引起的心率变异性抑制恢复不良。有慢性束缚应激史的 S1 对新的游泳应激源表现出皮质酮(CORT)反应减弱。相反,以前应激敏感的 S1 对急性束缚应激或消除训练表现出过度的 CORT 反应、对地塞米松挑战不敏感以及海马 CA3 糖皮质激素受体 mRNA 减少,表明下丘脑-垂体-肾上腺轴的负反馈控制下调。恐惧和消除回路中关键神经节点的神经元形态分析显示 S1 中的基底外侧杏仁核神经元的树突分支增大,但杏仁核内下皮质和前扣带皮质的树突分支正常。总的来说,这些数据为 S1 品系作为阐明持久、过度恐惧的神经、分子和遗传基础的可行模型的实用性提供了一致的支持。