Extinction of auditory fear conditioning requires MAPK/ERK activation in the basolateral amygdala

被引:167
作者
Herry, Cyril
Trifilieff, Pierre
Micheau, Jacques
Luethi, Andreas
Mons, Nicole
机构
[1] Friedrich Miescher Inst, CH-4058 Basel, Switzerland
[2] Univ Bordeaux 1, CNRS UMR 5106, Lab Neurosci Cognit, F-33405 Talence, France
关键词
U0126; amygdala; extinction; fear conditioning; MAP kinase;
D O I
10.1111/j.1460-9568.2006.04893.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Whereas the neuronal substrates underlying the acquisition of auditory fear conditioning have been widely studied, the substrates and mechanisms mediating the acquisition of fear extinction remain largely elusive. Previous reports indicate that consolidation of fear extinction depends on the mitogen-activated protein kinase/extracellular-signal regulated kinase (MAPK/ERK) signalling pathway and on protein synthesis in the medial prefrontal cortex (mPFC). Based on experiments using the fear-potentiated startle paradigm suggesting a role for neuronal plasticity in the basolateral amygdala (BLA) during fear extinction, we directly addressed whether MAPK/ERK signalling in the basolateral amygdala is necessary for the acquisition of fear extinction using conditioned freezing as a read-out. First, we investigated the regional and temporal pattern of MAPK/ERK activation in the BLA following extinction learning in C57Bl/6J mice. Our results indicate that acquisition of extinction is associated with an increase of phosphorylated MAPK/ERK in the BLA. Moreover, we found that inhibition of the MAPK/ERK signalling pathway by intrabasolateral amygdala infusion of the MEK inhibitor, U0126, completely blocks acquisition of extinction. Thus, our results indicate that the MAPK/ERK signalling pathway is required for extinction of auditory fear conditioning in the BLA, and support a role for neuronal plasticity in the BLA during the acquisition of fear extinction.
引用
收藏
页码:261 / 269
页数:9
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