Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex

被引:2
|
作者
Kong, Mi-Seon [1 ]
Kim, Namsoo [2 ]
Jo, Kyeong Im [3 ]
Kim, Sung -Phil [4 ]
Choi, June -Seek [3 ]
机构
[1] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA
[2] Howard Hughes Med Inst, Janelia Res Campus, Ashburn, VA 20147 USA
[3] Korea Univ, Sch Psychol, Seoul 02841, South Korea
[4] Ulsan Natl Inst Sci & Technol UNIST, Dept Biomed Engn, Ulsan 44919, South Korea
基金
新加坡国家研究基金会;
关键词
Fear; Memory; Conditioning; Entorhinal cortex; MEDIAL PREFRONTAL CORTEX; PERSISTENT ACTIVITY; PERIRHINAL CORTEX; NMDA RECEPTORS; SINGLE NEURONS; HIPPOCAMPUS; ASSOCIATION; CIRCUITS; AMYGDALA; CELLS;
D O I
10.5607/en22042
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Trace fear conditioning is characterized by a stimulus-free trace interval (TI) between the conditioned stimulus (CS) and the unconditioned stimu- lus (US), which requires an array of brain structures to support the formation and storage of associative memory. The entorhinal cortex (EC) has been proposed to provide essential neural code for resolving temporal discontinuity in conjunction with the hippocampus. However, how the CS and TI are encoded at the neuronal level in the EC is not clear. In Exp. 1, we tested the effect of bilateral pre-training electrolytic lesions of EC on trace vs. delay fear conditioning using rats as subjects. We found that the lesions impaired the acquisition of trace but not delay fear conditioning confirming that EC is a critical brain area for trace fear memory formation. In Exp. 2, single-unit activities from EC were recorded during the pre - training baseline and post-training retention sessions following trace or delay conditioning. The recording results showed that a significant propor- tion of the EC neurons modulated their firing during TI after the trace conditioning, but not after the delay fear conditioning. Further analysis re- vealed that the majority of modulated units decreased the firing rate during the TI or the CS. Taken together, these results suggest that EC critically contributes to trace fear conditioning by modulating neuronal activity during the TI to facilitate the association between the CS and US across a temporal gap.
引用
收藏
页码:20 / 30
页数:11
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