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Reactivating hippocampal-mediated memories during reconsolidation to disrupt fear

Memories are stored in the brain as cellular ensembles activated during learning and reactivated during retrieval. Using the Tet-tag system in mice, we label dorsal dentate gyrus neurons activated by positive, neutral or negative experiences with channelrhodopsin-2. Following fear-conditioning, thes...

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Autores principales: Grella, Stephanie L., Fortin, Amanda H., Ruesch, Evan, Bladon, John H., Reynolds, Leanna F., Gross, Abby, Shpokayte, Monika, Cincotta, Christine, Zaki, Yosif, Ramirez, Steve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468169/
https://www.ncbi.nlm.nih.gov/pubmed/36096993
http://dx.doi.org/10.1038/s41467-022-32246-8
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author Grella, Stephanie L.
Fortin, Amanda H.
Ruesch, Evan
Bladon, John H.
Reynolds, Leanna F.
Gross, Abby
Shpokayte, Monika
Cincotta, Christine
Zaki, Yosif
Ramirez, Steve
author_facet Grella, Stephanie L.
Fortin, Amanda H.
Ruesch, Evan
Bladon, John H.
Reynolds, Leanna F.
Gross, Abby
Shpokayte, Monika
Cincotta, Christine
Zaki, Yosif
Ramirez, Steve
author_sort Grella, Stephanie L.
collection PubMed
description Memories are stored in the brain as cellular ensembles activated during learning and reactivated during retrieval. Using the Tet-tag system in mice, we label dorsal dentate gyrus neurons activated by positive, neutral or negative experiences with channelrhodopsin-2. Following fear-conditioning, these cells are artificially reactivated during fear memory recall. Optical stimulation of a competing positive memory is sufficient to update the memory during reconsolidation, thereby reducing conditioned fear acutely and enduringly. Moreover, mice demonstrate operant responding for reactivation of a positive memory, confirming its rewarding properties. These results show that interference from a rewarding experience can counteract negative affective states. While memory-updating, induced by memory reactivation, involves a relatively small set of neurons, we also find that activating a large population of randomly labeled dorsal dentate gyrus neurons is effective in promoting reconsolidation. Importantly, memory-updating is specific to the fear memory. These findings implicate the dorsal dentate gyrus as a potential therapeutic node for modulating memories to suppress fear.
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spelling pubmed-94681692022-09-14 Reactivating hippocampal-mediated memories during reconsolidation to disrupt fear Grella, Stephanie L. Fortin, Amanda H. Ruesch, Evan Bladon, John H. Reynolds, Leanna F. Gross, Abby Shpokayte, Monika Cincotta, Christine Zaki, Yosif Ramirez, Steve Nat Commun Article Memories are stored in the brain as cellular ensembles activated during learning and reactivated during retrieval. Using the Tet-tag system in mice, we label dorsal dentate gyrus neurons activated by positive, neutral or negative experiences with channelrhodopsin-2. Following fear-conditioning, these cells are artificially reactivated during fear memory recall. Optical stimulation of a competing positive memory is sufficient to update the memory during reconsolidation, thereby reducing conditioned fear acutely and enduringly. Moreover, mice demonstrate operant responding for reactivation of a positive memory, confirming its rewarding properties. These results show that interference from a rewarding experience can counteract negative affective states. While memory-updating, induced by memory reactivation, involves a relatively small set of neurons, we also find that activating a large population of randomly labeled dorsal dentate gyrus neurons is effective in promoting reconsolidation. Importantly, memory-updating is specific to the fear memory. These findings implicate the dorsal dentate gyrus as a potential therapeutic node for modulating memories to suppress fear. Nature Publishing Group UK 2022-09-12 /pmc/articles/PMC9468169/ /pubmed/36096993 http://dx.doi.org/10.1038/s41467-022-32246-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Grella, Stephanie L.
Fortin, Amanda H.
Ruesch, Evan
Bladon, John H.
Reynolds, Leanna F.
Gross, Abby
Shpokayte, Monika
Cincotta, Christine
Zaki, Yosif
Ramirez, Steve
Reactivating hippocampal-mediated memories during reconsolidation to disrupt fear
title Reactivating hippocampal-mediated memories during reconsolidation to disrupt fear
title_full Reactivating hippocampal-mediated memories during reconsolidation to disrupt fear
title_fullStr Reactivating hippocampal-mediated memories during reconsolidation to disrupt fear
title_full_unstemmed Reactivating hippocampal-mediated memories during reconsolidation to disrupt fear
title_short Reactivating hippocampal-mediated memories during reconsolidation to disrupt fear
title_sort reactivating hippocampal-mediated memories during reconsolidation to disrupt fear
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468169/
https://www.ncbi.nlm.nih.gov/pubmed/36096993
http://dx.doi.org/10.1038/s41467-022-32246-8
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