Prefrontal dopamine regulates fear reinstatement through the downregulation of extinction circuits

被引:24
作者
Hitora-Imamura, Natsuko [1 ]
Miura, Yuki [1 ]
Teshirogi, Chie [1 ]
Ikegaya, Yuji [1 ,2 ]
Matsuki, Norio [1 ]
Nomura, Hiroshi [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Chem Pharmacol, Tokyo, Japan
[2] Ctr Informat & Neural Networks, Osaka, Japan
来源
ELIFE | 2015年 / 4卷
基金
日本学术振兴会;
关键词
FREELY-MOVING RATS; SYNAPTIC-TRANSMISSION; CONDITIONED FEAR; C-FOS; BASOLATERAL AMYGDALA; CENTRAL NUCLEUS; ANXIETY DISORDERS; DISSOCIABLE ROLES; PRELIMBIC CORTEX; EXPOSURE THERAPY;
D O I
10.7554/eLife.08274
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Prevention of relapses is a major challenge in treating anxiety disorders. Fear reinstatement can cause relapse in spite of successful fear reduction through extinction-based exposure therapy. By utilising a contextual fear-conditioning task in mice, we found that reinstatement was accompanied by decreased c-Fos expression in the infralimbic cortex (IL) with reduction of synaptic input and enhanced c-Fos expression in the medial subdivision of the central nucleus of the amygdala (CeM). Moreover, we found that IL dopamine plays a key role in reinstatement. A reinstatement-inducing reminder shock induced c-Fos expression in the IL-projecting dopaminergic neurons in the ventral tegmental area, and the blocking of IL D1 signalling prevented reduction of synaptic input, CeM c-Fos expression, and fear reinstatement. These findings demonstrate that a dopamine-dependent inactivation of extinction circuits underlies fear reinstatement and may explain the comorbidity of substance use disorders and anxiety disorders.
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页数:15
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