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Consolidation of fear extinction requires NMDA receptor-dependent bursting in the ventromedial prefrontal cortex.

机译:恐惧消除的巩固需要腹侧前额叶皮层中NMDA受体依赖性的爆发。

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Extinction of conditioned fear is an active learning process requiring N-methyl-D-aspartate receptors (NMDARs), but the timing, location, and neural mechanisms of NMDAR-mediated processing in extinction are a matter of debate. Here we show that infusion of the NMDAR antagonist CPP into the ventromedial prefrontal cortex (vmPFC) prior to, or immediately after, extinction training impaired 24 hr recall of extinction. These findings indicate that consolidation of extinction requires posttraining activation of NMDARs within the vmPFC. Using multichannel unit recording, we observed that CPP selectively reduced burst firing in vmPFC neurons, suggesting that bursting in vmPFC is necessary for consolidation of extinction. In support of this, we found that the degree of bursting in infralimbic vmPFC neurons shortly after extinction predicted subsequent recall of extinction. We suggest that NMDAR-dependent bursting in the infralimbic vmPFC initiates calcium-dependent molecular cascades that stabilize extinction memory, thereby allowing for successful recall of extinction.
机译:消除条件性恐惧是一个需要N-甲基-D-天冬氨酸受体(NMDARs)的活跃学习过程,但是NMDAR介导的灭绝过程的时机,位置和神经机制尚有争议。在这里,我们显示,在灭绝训练之前或之后,将NMDAR拮抗剂CPP注入腹侧前额叶皮层(vmPFC)会损害24小时的灭绝记忆。这些发现表明灭绝的巩固要求在vmPFC内对NMDAR进行训练后激活。使用多通道单位记录,我们观察到CPP有选择地减少了vmPFC神经元的爆发放电,这表明vmPFC爆发对于巩固灭绝是必要的。为此,我们发现灭绝后不久的下肢vmPFC神经元的爆发程度预示了随后的灭绝。我们建议在下缘的vmPFC中依赖NMDAR的爆发引发钙依赖性的分子级联反应,从而稳定灭绝记忆,从而使灭绝成功。

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