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Activation of cortical M(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating

Reactivated long-term memories can become labile and sensitive to modification. Memories in this destabilized state can be weakened or strengthened, but there is limited research characterizing the mechanisms underlying retrieval-induced qualitative updates (i.e., information integration). We have p...

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Autores principales: Jardine, Kristen H., Wideman, Cassidy E., MacGregor, Chelsea, Sgarbossa, Cassandra, Orr, Dean, Mitchnick, Krista A., Winters, Boyer D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280228/
https://www.ncbi.nlm.nih.gov/pubmed/32514039
http://dx.doi.org/10.1038/s41598-020-65836-x
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author Jardine, Kristen H.
Wideman, Cassidy E.
MacGregor, Chelsea
Sgarbossa, Cassandra
Orr, Dean
Mitchnick, Krista A.
Winters, Boyer D.
author_facet Jardine, Kristen H.
Wideman, Cassidy E.
MacGregor, Chelsea
Sgarbossa, Cassandra
Orr, Dean
Mitchnick, Krista A.
Winters, Boyer D.
author_sort Jardine, Kristen H.
collection PubMed
description Reactivated long-term memories can become labile and sensitive to modification. Memories in this destabilized state can be weakened or strengthened, but there is limited research characterizing the mechanisms underlying retrieval-induced qualitative updates (i.e., information integration). We have previously implicated cholinergic transmission in object memory destabilization. Here we present a novel rodent paradigm developed to assess the role of this cholinergic mechanism in qualitative object memory updating. The post-reactivation object memory modification (PROMM) task exposes rats to contextual information following object memory reactivation. Subsequent object exploratory performance suggests that the contextual information is integrated with the original memory in a reactivation- and time-dependent manner. This effect is blocked by interference with M(1) muscarinic receptors and several downstream signals in perirhinal cortex. These findings therefore demonstrate a hitherto unacknowledged cognitive function for acetylcholine with important implications for understanding the dynamic nature of long-term memory storage in the normal and aging brain.
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spelling pubmed-72802282020-06-15 Activation of cortical M(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating Jardine, Kristen H. Wideman, Cassidy E. MacGregor, Chelsea Sgarbossa, Cassandra Orr, Dean Mitchnick, Krista A. Winters, Boyer D. Sci Rep Article Reactivated long-term memories can become labile and sensitive to modification. Memories in this destabilized state can be weakened or strengthened, but there is limited research characterizing the mechanisms underlying retrieval-induced qualitative updates (i.e., information integration). We have previously implicated cholinergic transmission in object memory destabilization. Here we present a novel rodent paradigm developed to assess the role of this cholinergic mechanism in qualitative object memory updating. The post-reactivation object memory modification (PROMM) task exposes rats to contextual information following object memory reactivation. Subsequent object exploratory performance suggests that the contextual information is integrated with the original memory in a reactivation- and time-dependent manner. This effect is blocked by interference with M(1) muscarinic receptors and several downstream signals in perirhinal cortex. These findings therefore demonstrate a hitherto unacknowledged cognitive function for acetylcholine with important implications for understanding the dynamic nature of long-term memory storage in the normal and aging brain. Nature Publishing Group UK 2020-06-08 /pmc/articles/PMC7280228/ /pubmed/32514039 http://dx.doi.org/10.1038/s41598-020-65836-x 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
Jardine, Kristen H.
Wideman, Cassidy E.
MacGregor, Chelsea
Sgarbossa, Cassandra
Orr, Dean
Mitchnick, Krista A.
Winters, Boyer D.
Activation of cortical M(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating
title Activation of cortical M(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating
title_full Activation of cortical M(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating
title_fullStr Activation of cortical M(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating
title_full_unstemmed Activation of cortical M(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating
title_short Activation of cortical M(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating
title_sort activation of cortical m(1) muscarinic receptors and related intracellular signaling is necessary for reactivation-induced object memory updating
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280228/
https://www.ncbi.nlm.nih.gov/pubmed/32514039
http://dx.doi.org/10.1038/s41598-020-65836-x
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