IFEC-CONICET, Departamento de Farmacología, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.
Departamento de Farmacologia, CCB, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.
Neurobiol Learn Mem. 2018 Nov;155:412-421. doi: 10.1016/j.nlm.2018.09.002. Epub 2018 Sep 6.
Fear extinction is defined as a decline in fear-conditioned responses following non-reinforced exposure to a fear conditioned stimulus, therefore the conditioned stimulus gains new predictive properties. Patients with anxiety related disorders (e.g.: PTSD) subjected to extinction-like exposure treatments often experience a relapse of symptoms. Stress is a risk factor for those psychiatric disorders and a critical modulator of fear learning that turns the memory resistant to the extinction process. Dendritic spines are the anatomical sites where neuronal activity reshapes brain networks during learning and memory processes. Thus, we planned to characterize the dynamics of synaptic remodeling before and after contextual fear extinction in the dorsal hippocampus (DH), and how this process is affected by a previous stress experience. Animals with or without previous stress were contextually fear conditioned and one day later trained in an extinction paradigm. Rats were sacrificed one day after conditioning (pre-extinction) or one day after extinction for spine density analysis in the DH. We confirmed that stress exposure induced a deficit in extinction learning. Further, a higher density of dendritic spines, particularly mature ones, was observed in the DH of non-stressed conditioned animals at pre-extinction. Interestingly, after extinction, the spine levels returned to the control values. Conversely, stressed animals did not show such spines boost (pre-extinction) or any other change (post-extinction). In contrast, such standard dynamics of dendritic changes as well as the behavioral extinction was recovered when stressed animals received an intra-basolateral amygdala infusion of midazolam prior to stress. Altogether, these findings suggest that stress hinders the normal dynamic of dendritic remodeling after fear extinction and this could be part of the neurobiological substrate that makes those memories resistant to be extinguished.
恐惧消退是指在非强化暴露于恐惧条件刺激后,恐惧条件反应的下降,因此条件刺激获得了新的预测属性。患有焦虑相关障碍(例如 PTSD)的患者接受类似消退的暴露治疗后,常出现症状复发。应激是这些精神障碍的一个风险因素,也是恐惧学习的关键调节剂,使记忆对消退过程产生抗性。树突棘是神经元活动在学习和记忆过程中重塑大脑网络的解剖部位。因此,我们计划在背侧海马体(DH)中描述恐惧消退前后突触重塑的动力学,以及这一过程如何受到先前应激体验的影响。有或没有先前应激的动物进行情境恐惧条件化,一天后在消退范式中进行训练。在条件化后一天(消退前)或消退后一天,对 DH 中的棘密度进行分析,以确定动物是否进行了条件化。我们证实,应激暴露会导致消退学习的缺陷。进一步,在非应激条件化动物的 DH 中,在消退前观察到树突棘密度增加,尤其是成熟的树突棘密度增加。有趣的是,在消退后,棘突水平恢复到对照值。相反,应激动物在消退前或消退后都没有表现出这种棘突增加(消退前)或任何其他变化(消退后)。相比之下,当应激动物在应激前接受内侧基底外侧杏仁核中咪达唑仑输注时,它们的树突变化和行为消退的这种标准动力学得以恢复。总之,这些发现表明,应激会阻碍恐惧消退后树突重塑的正常动态,这可能是使这些记忆难以消除的神经生物学基础的一部分。