Post-retrieval late process contributes to persistence of reactivated fear memory

被引:15
|
作者
Nakayama, Daisuke [1 ]
Yamasaki, Yoshiko [1 ]
Matsuki, Norio [1 ]
Nomura, Hiroshi [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Chem Pharmacol Lab, Bunkyo Ku, Tokyo 1130033, Japan
关键词
LONG-TERM-MEMORY; PROTEIN-SYNTHESIS INHIBITOR; MESSENGER-RNA SYNTHESIS; STRUCTURAL PLASTICITY; BASOLATERAL AMYGDALA; DENDRITIC SPINES; RECONSOLIDATION; CONSOLIDATION; HIPPOCAMPUS; REQUIRES;
D O I
10.1101/lm.029660.112
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several studies have demonstrated the mechanisms involved in memory persistence after learning. However, little is known about memory persistence after retrieval. In this study, a protein synthesis inhibitor, anisomycin, was infused into the basolateral amygdala of mice 9.5 h after retrieval of contextual conditioned fear. Anisomycin attenuated fear memory after 7 d, but not after 2 d. In contrast, infusion of anisomycin 5- or 24-h post-retrieval was ineffective. These findings indicate that anisomycin attenuates the persistence of reactivated fear memory in a time-dependent manner. We propose that late protein synthesis is required for memory persistence after retrieval.
引用
收藏
页码:307 / 310
页数:4
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