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The interhemispheric CA1 circuit governs rapid generalisation but not fear memory

Encoding specificity theory predicts most effective recall by the original conditions at encoding, while generalization endows recall flexibly under circumstances which deviate from the originals. The CA1 regions have been implicated in memory and generalization but whether and which locally separat...

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Autores principales: Zhou, Heng, Xiong, Gui-Jing, Jing, Liang, Song, Ning-Ning, Pu, De-Lin, Tang, Xun, He, Xiao-Bing, Xu, Fu-Qiang, Huang, Jing-Fei, Li, Ling-Jiang, Richter-Levin, Gal, Mao, Rong-Rong, Zhou, Qi-Xin, Ding, Yu-Qiang, Xu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736595/
https://www.ncbi.nlm.nih.gov/pubmed/29259187
http://dx.doi.org/10.1038/s41467-017-02315-4
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author Zhou, Heng
Xiong, Gui-Jing
Jing, Liang
Song, Ning-Ning
Pu, De-Lin
Tang, Xun
He, Xiao-Bing
Xu, Fu-Qiang
Huang, Jing-Fei
Li, Ling-Jiang
Richter-Levin, Gal
Mao, Rong-Rong
Zhou, Qi-Xin
Ding, Yu-Qiang
Xu, Lin
author_facet Zhou, Heng
Xiong, Gui-Jing
Jing, Liang
Song, Ning-Ning
Pu, De-Lin
Tang, Xun
He, Xiao-Bing
Xu, Fu-Qiang
Huang, Jing-Fei
Li, Ling-Jiang
Richter-Levin, Gal
Mao, Rong-Rong
Zhou, Qi-Xin
Ding, Yu-Qiang
Xu, Lin
author_sort Zhou, Heng
collection PubMed
description Encoding specificity theory predicts most effective recall by the original conditions at encoding, while generalization endows recall flexibly under circumstances which deviate from the originals. The CA1 regions have been implicated in memory and generalization but whether and which locally separated mechanisms are involved is not clear. We report here that fear memory is quickly formed, but generalization develops gradually over 24 h. Generalization but not fear memory is impaired by inhibiting ipsilateral (ips) or contralateral (con) CA1, and by optogenetic silencing of the ipsCA1 projections onto conCA1. By contrast, in vivo fEPSP recordings reveal that ipsCA1–conCA1 synaptic efficacy is increased with delay over 24 h when generalization is formed but it is unchanged if generalization is disrupted. Direct excitation of ipsCA1–conCA1 synapses using chemogenetic hM3Dq facilitates generalization formation. Thus, rapid generalization is an active process dependent on bilateral CA1 regions, and encoded by gradual synaptic learning in ipsCA1–conCA1 circuit.
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spelling pubmed-57365952017-12-21 The interhemispheric CA1 circuit governs rapid generalisation but not fear memory Zhou, Heng Xiong, Gui-Jing Jing, Liang Song, Ning-Ning Pu, De-Lin Tang, Xun He, Xiao-Bing Xu, Fu-Qiang Huang, Jing-Fei Li, Ling-Jiang Richter-Levin, Gal Mao, Rong-Rong Zhou, Qi-Xin Ding, Yu-Qiang Xu, Lin Nat Commun Article Encoding specificity theory predicts most effective recall by the original conditions at encoding, while generalization endows recall flexibly under circumstances which deviate from the originals. The CA1 regions have been implicated in memory and generalization but whether and which locally separated mechanisms are involved is not clear. We report here that fear memory is quickly formed, but generalization develops gradually over 24 h. Generalization but not fear memory is impaired by inhibiting ipsilateral (ips) or contralateral (con) CA1, and by optogenetic silencing of the ipsCA1 projections onto conCA1. By contrast, in vivo fEPSP recordings reveal that ipsCA1–conCA1 synaptic efficacy is increased with delay over 24 h when generalization is formed but it is unchanged if generalization is disrupted. Direct excitation of ipsCA1–conCA1 synapses using chemogenetic hM3Dq facilitates generalization formation. Thus, rapid generalization is an active process dependent on bilateral CA1 regions, and encoded by gradual synaptic learning in ipsCA1–conCA1 circuit. Nature Publishing Group UK 2017-12-19 /pmc/articles/PMC5736595/ /pubmed/29259187 http://dx.doi.org/10.1038/s41467-017-02315-4 Text en © The Author(s) 2017 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
Zhou, Heng
Xiong, Gui-Jing
Jing, Liang
Song, Ning-Ning
Pu, De-Lin
Tang, Xun
He, Xiao-Bing
Xu, Fu-Qiang
Huang, Jing-Fei
Li, Ling-Jiang
Richter-Levin, Gal
Mao, Rong-Rong
Zhou, Qi-Xin
Ding, Yu-Qiang
Xu, Lin
The interhemispheric CA1 circuit governs rapid generalisation but not fear memory
title The interhemispheric CA1 circuit governs rapid generalisation but not fear memory
title_full The interhemispheric CA1 circuit governs rapid generalisation but not fear memory
title_fullStr The interhemispheric CA1 circuit governs rapid generalisation but not fear memory
title_full_unstemmed The interhemispheric CA1 circuit governs rapid generalisation but not fear memory
title_short The interhemispheric CA1 circuit governs rapid generalisation but not fear memory
title_sort interhemispheric ca1 circuit governs rapid generalisation but not fear memory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736595/
https://www.ncbi.nlm.nih.gov/pubmed/29259187
http://dx.doi.org/10.1038/s41467-017-02315-4
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