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Excitation of prefrontal cortical neurons during conditioning enhances fear memory formation

Animals can remember a situation associated with an aversive event. Contextual fear memory is initially encoded and consolidated in the hippocampus and gradually consolidated in multiple brain regions over time, including the medial prefrontal cortex (PFC). However, it is not fully understood how PF...

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Autores principales: Shibano, Natsumi, Yamazaki, Mio, Arima, Tomoki, Abe, Konami, Kuroda, Marin, Kobayashi, Yuki, Itohara, Shigeyoshi, Furuichi, Teiichi, Sano, Yoshitake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248099/
https://www.ncbi.nlm.nih.gov/pubmed/32451463
http://dx.doi.org/10.1038/s41598-020-65597-7
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author Shibano, Natsumi
Yamazaki, Mio
Arima, Tomoki
Abe, Konami
Kuroda, Marin
Kobayashi, Yuki
Itohara, Shigeyoshi
Furuichi, Teiichi
Sano, Yoshitake
author_facet Shibano, Natsumi
Yamazaki, Mio
Arima, Tomoki
Abe, Konami
Kuroda, Marin
Kobayashi, Yuki
Itohara, Shigeyoshi
Furuichi, Teiichi
Sano, Yoshitake
author_sort Shibano, Natsumi
collection PubMed
description Animals can remember a situation associated with an aversive event. Contextual fear memory is initially encoded and consolidated in the hippocampus and gradually consolidated in multiple brain regions over time, including the medial prefrontal cortex (PFC). However, it is not fully understood how PFC neurons contribute to contextual fear memory formation during learning. In the present study, neuronal activity was increased in PFC neurons utilizing the pharmacogenetic hM3Dq-system in male mice. We show that fear expression and memory formation are enhanced by increasing neuronal activity in PFC during conditioning phase. Previous studies showed that the activation of hM3Dq receptor in a subset of amygdala neurons enhanced fear memory formation and biased which neurons are allocated to a memory trace, in which immediate early gene c-fos was preferentially expressed following memory retrieval in these pre-activated neurons. In this study, hM3Dq activation in PFC could not change the probability of c-fos expression in pre-activated neurons flowing memory retrieval. Instead, the number c-fos positive neurons following memory retrieval was significantly increased in the basolateral amygdala. Our results suggest that neuronal activity in PFC at the time of learning modulates fear memory formation and downstream cellular activity at an early phase.
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spelling pubmed-72480992020-06-04 Excitation of prefrontal cortical neurons during conditioning enhances fear memory formation Shibano, Natsumi Yamazaki, Mio Arima, Tomoki Abe, Konami Kuroda, Marin Kobayashi, Yuki Itohara, Shigeyoshi Furuichi, Teiichi Sano, Yoshitake Sci Rep Article Animals can remember a situation associated with an aversive event. Contextual fear memory is initially encoded and consolidated in the hippocampus and gradually consolidated in multiple brain regions over time, including the medial prefrontal cortex (PFC). However, it is not fully understood how PFC neurons contribute to contextual fear memory formation during learning. In the present study, neuronal activity was increased in PFC neurons utilizing the pharmacogenetic hM3Dq-system in male mice. We show that fear expression and memory formation are enhanced by increasing neuronal activity in PFC during conditioning phase. Previous studies showed that the activation of hM3Dq receptor in a subset of amygdala neurons enhanced fear memory formation and biased which neurons are allocated to a memory trace, in which immediate early gene c-fos was preferentially expressed following memory retrieval in these pre-activated neurons. In this study, hM3Dq activation in PFC could not change the probability of c-fos expression in pre-activated neurons flowing memory retrieval. Instead, the number c-fos positive neurons following memory retrieval was significantly increased in the basolateral amygdala. Our results suggest that neuronal activity in PFC at the time of learning modulates fear memory formation and downstream cellular activity at an early phase. Nature Publishing Group UK 2020-05-25 /pmc/articles/PMC7248099/ /pubmed/32451463 http://dx.doi.org/10.1038/s41598-020-65597-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shibano, Natsumi
Yamazaki, Mio
Arima, Tomoki
Abe, Konami
Kuroda, Marin
Kobayashi, Yuki
Itohara, Shigeyoshi
Furuichi, Teiichi
Sano, Yoshitake
Excitation of prefrontal cortical neurons during conditioning enhances fear memory formation
title Excitation of prefrontal cortical neurons during conditioning enhances fear memory formation
title_full Excitation of prefrontal cortical neurons during conditioning enhances fear memory formation
title_fullStr Excitation of prefrontal cortical neurons during conditioning enhances fear memory formation
title_full_unstemmed Excitation of prefrontal cortical neurons during conditioning enhances fear memory formation
title_short Excitation of prefrontal cortical neurons during conditioning enhances fear memory formation
title_sort excitation of prefrontal cortical neurons during conditioning enhances fear memory formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248099/
https://www.ncbi.nlm.nih.gov/pubmed/32451463
http://dx.doi.org/10.1038/s41598-020-65597-7
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