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首页> 外文期刊>Biological psychiatry >Neurobiological basis of failure to recall extinction memory in posttraumatic stress disorder.
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Neurobiological basis of failure to recall extinction memory in posttraumatic stress disorder.

机译:创伤后应激障碍未能唤起灭绝记忆的神经生物学基础。

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摘要

BACKGROUND: A clinical characteristic of posttraumatic stress disorder (PTSD) is persistently elevated fear responses to stimuli associated with the traumatic event. The objective herein is to determine whether extinction of fear responses is impaired in PTSD and whether such impairment is related to dysfunctional activation of brain regions known to be involved in fear extinction, viz., amygdala, hippocampus, ventromedial prefrontal cortex (vmPFC), and dorsal anterior cingulate cortex (dACC). METHODS: Sixteen individuals diagnosed with PTSD and 15 trauma-exposed non-PTSD control subjects underwent a 2-day fear conditioning and extinction protocol in a 3-T functional magnetic resonance imaging scanner. Conditioning and extinction training were conducted on day 1. Extinction recall (or extinction memory) test was conducted on day 2 (extinguished conditioned stimuli presented in the absence of shock). Skin conductance response (SCR) was scored throughout the experiment as an index of the conditioned response. RESULTS: The SCR data revealed no significant differences between groups during acquisition and extinction of conditioned fear on day 1. On day 2, however, PTSD subjects showed impaired recall of extinction memory. Analysis of functional magnetic resonance imaging data showed greater amygdala activation in the PTSD group during day 1 extinction learning. During extinction recall, lesser activation in hippocampus and vmPFC and greater activation in dACC were observed in the PTSD group. The magnitude of extinction memory across all subjects was correlated with activation of hippocampus and vmPFC during extinction recall testing. CONCLUSIONS: These findings support the hypothesis that fear extinction is impaired in PTSD. They further suggest that dysfunctional activation in brain structures that mediate fear extinction learning, and especially its recall, underlie this impairment.
机译:背景:创伤后应激障碍(PTSD)的临床特征是对与创伤事件相关的刺激的恐惧反应持续升高。本文的目的是确定在PTSD中恐惧反应的消除是否受损,以及这种损害是否与已知参与恐惧消除的杏仁区域,杏仁核,海马,腹膜前额叶皮层(vmPFC)的功能异常激活有关,以及背前扣带回皮层(dACC)。方法:在3-T功能磁共振成像扫描仪中,对16名被诊断为PTSD的个体和15名暴露于非PTSD的对照受试者进行了为期2天的恐惧条件和消光方案。在第1天进行条件和灭绝训练。在第2天进行灭绝回想(或灭绝记忆)测试(在没有电击的情况下熄灭的条件刺激)。在整个实验中对皮肤电导反应(SCR)进行评分,作为条件反应的指标。结果:SCR数据显示第1天在获得和消除条件性恐惧的过程中各组之间无显着差异。然而,在第2天,PTSD受试者显示了对记忆消失的记忆受损。功能磁共振成像数据分析显示,在第1天的消光学习过程中,PTSD组的杏仁核活化程度更高。在灭绝记忆中,PTSD组的海马和vmPFC激活较少,而dACC激活较大。在灭绝回忆测试期间,所有受试者的灭绝记忆大小与海马和vmPFC的激活相关。结论:这些发现支持以下假设,即在PTSD中恐惧绝种受损。他们进一步表明,介导恐惧绝种学习,尤其是其回忆的大脑结构失调激活是这种损害的基础。

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