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创伤后应激障碍可能与恐惧抑制受损有关:与症状严重程度的关系。

Posttraumatic stress disorder may be associated with impaired fear inhibition: relation to symptom severity.

作者信息

Jovanovic Tanja, Norrholm Seth D, Fennell Jennifer E, Keyes Megan, Fiallos Ana M, Myers Karyn M, Davis Michael, Duncan Erica J

机构信息

Mental Health Service, Atlanta Veterans' Affairs Medical Center, Decatur, GA 30033, USA.

出版信息

Psychiatry Res. 2009 May 15;167(1-2):151-60. doi: 10.1016/j.psychres.2007.12.014. Epub 2009 Apr 5.

Abstract

One of the central problems in posttraumatic stress disorder (PTSD) is the inability to suppress fear even under safe conditions. The neural underpinnings of fear are clinically relevant but poorly understood. This study assessed fear potentiation and fear inhibition using fear-potentiated startle in a conditional discrimination procedure (AX+/BX-). We hypothesized that patients with PTSD would show normal fear potentiation and impaired fear inhibition. Subjects comprised 28 healthy volunteers and 27 PTSD patients (14 with low current symptoms, 13 with high current symptoms) who were presented with one set of colored lights (AX trials) paired with aversive air blasts to the throat, and a different series of lights (BX trials) presented without air blasts. We then presented A and B together (AB trials) to see whether B would inhibit fear potentiation to A. All groups showed robust fear potentiation in that they had significantly greater startle magnitude on AX trials than on noise-alone trials. However, the high-symptom PTSD group did not show fear inhibition: these subjects had significantly greater fear potentiation on the AB trials than both the controls and the low-symptom PTSD patients.

摘要

创伤后应激障碍(PTSD)的核心问题之一是即使在安全条件下也无法抑制恐惧。恐惧的神经基础具有临床相关性,但了解甚少。本研究在条件辨别程序(AX+/BX-)中使用恐惧增强惊吓反应来评估恐惧增强和恐惧抑制。我们假设PTSD患者会表现出正常的恐惧增强和受损的恐惧抑制。研究对象包括28名健康志愿者和27名PTSD患者(14名当前症状较轻,13名当前症状较重),他们观看一组与吹向喉咙的厌恶性气团配对的彩色灯光(AX试验),以及另一组不伴有气团的不同系列灯光(BX试验)。然后我们同时呈现A和B(AB试验),以观察B是否会抑制对A的恐惧增强。所有组都表现出强烈的恐惧增强,因为他们在AX试验中的惊吓幅度明显大于仅噪声试验。然而,高症状PTSD组没有表现出恐惧抑制:这些受试者在AB试验中的恐惧增强明显大于对照组和低症状PTSD患者。

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