Pharmacological facilitation of fear extinction and the search for adjunct treatments for anxiety disorders - the case of yohimbine

被引:89
作者
Holmes, Andrew [1 ]
Quirk, Gregory J. [2 ,3 ]
机构
[1] NIAAA, Sect Behav Sci & Genet, Lab Integrat Neurosci, NIH, Bethesda, MD 20852 USA
[2] Univ Puerto Rico, Sch Med, Dept Psychiat, San Juan, PR 00936 USA
[3] Univ Puerto Rico, Sch Med, Dept Anat & Neurobiol, San Juan, PR 00936 USA
关键词
CONDITIONED FEAR; SEROTONIN TRANSPORTER; FRONTAL-CORTEX; INFRALIMBIC CORTEX; INDUCED INCREASES; 5-HT1A RECEPTORS; D-CYCLOSERINE; STRESS; RATS; NORADRENALINE;
D O I
10.1016/j.tips.2009.10.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
There is current interest in identifying drugs that facilitate fear extinction, as this form of learning is the basis of certain cognitive therapies for anxiety disorders. Following an initial report several years ago that the alpha 2-adrenoreceptor antagonist yohimbine facilitated extinction in mice, more recent studies have shown mixed effects or even impairment. It has become clear that the effect of yohimbine on extinction depends on a number of factors, including genetic background, contextual variables and the presence of competing behaviors. To what extent theses effects of yohimbine are mediated through the alpha 2-adrenoreceptor, as opposed to other sites of action, is also uncertain. More work is needed before this drug can be approved as a pharmacological adjunct for extinction-based therapies. More generally, the case of yohimbine may serve as a model for the development of other extinction facilitators.
引用
收藏
页码:2 / 7
页数:6
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