Potentiation of GluN2C/D NMDA Receptor Subtypes in the Amygdala Facilitates the Retention of Fear and Extinction Learning in Mice

被引:44
作者
Ogden, Kevin K. [1 ]
Khatri, Alpa [1 ]
Traynelis, Stephen F. [1 ]
Heldt, Scott A. [2 ,3 ]
机构
[1] Emory Univ, Dept Pharmacol, Atlanta, GA 30322 USA
[2] Univ Tennessee, Hlth Sci Ctr, Dept Anat & Neurobiol, Memphis, TN 38163 USA
[3] Univ Tennessee, Hlth Sci Ctr, Inst Neurosci, Memphis, TN 38163 USA
关键词
extinction; fear; NMDA; D-cycloserine; GluN2C; GluN2D; LONG-TERM POTENTIATION; KAPPA-OPIOID RECEPTORS; D-ASPARTATE RECEPTOR; D-CYCLOSERINE; CONDITIONED FEAR; BASOLATERAL AMYGDALA; SYNAPTIC-TRANSMISSION; PREPULSE INHIBITION; 5-HT6; RECEPTORS; PARTIAL AGONIST;
D O I
10.1038/npp.2013.241
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
NMDA receptors are glutamate receptor ion channels that contribute to synaptic plasticity and are important for many forms of learning and memory. In the amygdala, NMDA receptors are critical for the acquisition, retention, and extinction of classically conditioned fear responses. Although the GluN2B subunit has been implicated in both the acquisition and extinction of conditioned fear, GluN2C-knockout mice show reduced conditioned fear responses. Moreover, D-cycloserine ( DCS), which facilitates fear extinction, selectively enhances the activity of GluN2C-containing NMDA receptors. To further define the contribution of GluN2C receptors to fear learning, we infused the GluN2C/GluN2D-selective potentiator CIQ bilaterally into the basolateral amygdala ( 3, 10, or 30 mu g/side) following either fear conditioning or fear extinction training. CIQ both increased the expression of conditioned fear 24 h later and enhanced the extinction of the previously conditioned fear response. These results support a critical role for GluN2C receptors in the amygdala in the consolidation of learned fear responses and suggest that increased activity of GluN2C receptors may underlie the therapeutic actions of DCS.
引用
收藏
页码:625 / 637
页数:13
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