Morphine prevents the development of stress-enhanced fear learning

被引:33
作者
Szczytkowski-Thomson, Jennifer L. [1 ,2 ]
Lebonville, Christina L. [1 ]
Lysle, Donald T. [1 ]
机构
[1] Univ N Carolina, Dept Psychol, Chapel Hill, NC 27599 USA
[2] Messiah Coll, Dept Psychol, Mechanicsburg, PA 17055 USA
基金
美国国家卫生研究院;
关键词
Morphine; Post-traumatic stress disorder; Stress-enhanced fear learning; Fear conditioning; Foot shock; KINASE M-ZETA; POSTTRAUMATIC-STRESS; MEMORY PROCESSES; DISORDER; HIPPOCAMPUS; RATS; RESPONSES; EXPOSURE; AMYGDALA; INTERLEUKIN-1-BETA;
D O I
10.1016/j.pbb.2012.10.013
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The current study investigates the pharmacotherapeutic use of morphine as a preventative treatment for stress-enhanced fear learning, an animal model that closely mimics symptoms of post-traumatic stress disorder (PTSD). PTSD is a chronic and debilitating anxiety disorder characterized by exaggerated fear and/or anxiety that may develop as a result of exposure to a traumatic event. In this model, rats are exposed to a severe stressor (15 foot shocks) in one environment (Context A) and then subsequently exposed to a milder form of the same stressor (single foot shock) in a different environment (Context B). Animals that did not receive prior shock treatment exhibit fear responsiveness to Context B in line with the severity of the single shock given in this context. Animals that had received prior shock treatment in Context A exhibit an exaggerated learned fear response to Context B. Furthermore, animals receiving a single dose of morphine immediately following the severe stressor in Context A continue to show an enhanced fear response in Context B. However, animals receiving repeated morphine administration (three injections) after exposure to the severe stressor in Context A or a single dose of morphine at 48 h after the severe stressor no longer exhibit an enhancement in fear learning to Context B. These results are consistent with clinical studies suggesting that morphine treatment following a severe stressor may be useful in preventing or reducing the severity of PTSD in at-risk populations. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:672 / 677
页数:6
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