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恐惧消退能否增强?药理学与行为学研究结果综述。

Can fear extinction be enhanced? A review of pharmacological and behavioral findings.

作者信息

Fitzgerald Paul J, Seemann Jocelyn R, Maren Stephen

机构信息

Department of Psychology, Texas A&M University, College Station, TX 77843-4235, United States.

Institute for Neuroscience, Texas A&M University, College Station, TX 77843-4235, United States.

出版信息

Brain Res Bull. 2014 Jun;105:46-60. doi: 10.1016/j.brainresbull.2013.12.007. Epub 2013 Dec 25.

DOI:10.1016/j.brainresbull.2013.12.007
PMID:24374101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4039692/
Abstract

There is considerable interest, from both a basic and clinical standpoint, in gaining a greater understanding of how pharmaceutical or behavioral manipulations alter fear extinction in animals. Not only does fear extinction in rodents model exposure therapy in humans, where the latter is a cornerstone of behavioral intervention for anxiety disorders such as post-traumatic stress disorder and specific phobias, but also understanding more about extinction provides basic information into learning and memory processes and their underlying circuitry. In this paper, we briefly review three principal approaches that have been used to modulate extinction processes in animals and humans: a purely pharmacological approach, the more widespread approach of combining pharmacology with behavior, and a purely behavioral approach. The pharmacological studies comprise modulation by: brain derived neurotrophic factor (BDNF), d-cycloserine, serotonergic and noradrenergic drugs, neuropeptides, endocannabinoids, glucocorticoids, histone deacetylase (HDAC) inhibitors, and others. These studies strongly suggest that extinction can be modulated by drugs, behavioral interventions, or their combination, although not always in a lasting manner. We suggest that pharmacotherapeutic manipulations provide considerable promise for promoting effective and lasting fear reduction in individuals with anxiety disorders. This article is part of a Special Issue entitled 'Memory enhancement'.

摘要

从基础和临床角度来看,人们对更深入了解药物或行为操作如何改变动物的恐惧消退有着浓厚兴趣。啮齿动物的恐惧消退不仅是人类暴露疗法的模型,而暴露疗法是创伤后应激障碍和特定恐惧症等焦虑症行为干预的基石,而且对消退的更多了解还能为学习和记忆过程及其潜在神经回路提供基础信息。在本文中,我们简要回顾三种用于调节动物和人类消退过程的主要方法:纯粹的药理学方法、药理学与行为相结合的更广泛方法以及纯粹的行为方法。药理学研究包括通过以下物质进行调节:脑源性神经营养因子(BDNF)、d - 环丝氨酸、血清素能和去甲肾上腺素能药物、神经肽、内源性大麻素、糖皮质激素、组蛋白脱乙酰酶(HDAC)抑制剂等。这些研究有力地表明,消退可以通过药物、行为干预或它们的组合来调节,尽管并非总是能持久。我们认为药物治疗操作在促进焦虑症患者有效且持久地减轻恐惧方面具有很大潜力。本文是名为“记忆增强”的特刊的一部分。

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Extinction during reconsolidation of threat memory diminishes prefrontal cortex involvement.威胁记忆再巩固过程中的消除会减少前额叶皮层的参与。
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Extinction of reinstated or ABC renewed fear responses renders them resistant to subsequent ABA renewal.恢复的或ABC重新引发的恐惧反应的消退使它们对随后的ABA重新出现具有抗性。
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