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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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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. |
format | Online Article Text |
id | pubmed-5736595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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