File Download

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

김성필

Kim, Sung-Phil
Brain-Computer Interface Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 30 -
dc.citation.number 1 -
dc.citation.startPage 20 -
dc.citation.title EXPERIMENTAL NEUROBIOLOGY -
dc.citation.volume 32 -
dc.contributor.author Kong, Mi-Seon -
dc.contributor.author Kim, Namsoo -
dc.contributor.author Jo, Kyeong Im -
dc.contributor.author Kim, Sung-Phil -
dc.contributor.author Choi, June -Seek -
dc.date.accessioned 2023-12-21T13:06:34Z -
dc.date.available 2023-12-21T13:06:34Z -
dc.date.created 2023-04-25 -
dc.date.issued 2023-02 -
dc.description.abstract 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. -
dc.identifier.bibliographicCitation EXPERIMENTAL NEUROBIOLOGY, v.32, no.1, pp.20 - 30 -
dc.identifier.doi 10.5607/en22042 -
dc.identifier.issn 1226-2560 -
dc.identifier.scopusid 2-s2.0-85153247537 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/64237 -
dc.identifier.wosid 000958503600003 -
dc.language 영어 -
dc.publisher KOREAN SOC BRAIN & NEURAL SCIENCE, KOREAN SOC NEURODEGENERATIVE DISEASE -
dc.title Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Medicine, Research & Experimental; Neurosciences -
dc.identifier.kciid ART002939298 -
dc.relation.journalResearchArea Research & Experimental Medicine; Neurosciences & Neurology -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.description.journalRegisteredClass kci -
dc.subject.keywordAuthor Fear -
dc.subject.keywordAuthor Memory -
dc.subject.keywordAuthor Conditioning -
dc.subject.keywordAuthor Entorhinal cortex -
dc.subject.keywordPlus MEDIAL PREFRONTAL CORTEX -
dc.subject.keywordPlus PERSISTENT ACTIVITY -
dc.subject.keywordPlus PERIRHINAL CORTEX -
dc.subject.keywordPlus NMDA RECEPTORS -
dc.subject.keywordPlus SINGLE NEURONS -
dc.subject.keywordPlus HIPPOCAMPUS -
dc.subject.keywordPlus ASSOCIATION -
dc.subject.keywordPlus CIRCUITS -
dc.subject.keywordPlus AMYGDALA -
dc.subject.keywordPlus CELLS -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.