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Cholinergic manipulations bidirectionally regulate object memory destabilization
Consolidated memories can become destabilized and open to modification upon retrieval. Destabilization is most reliably prompted when novel information is present during memory reactivation. We hypothesized that the neurotransmitter acetylcholine (ACh) plays an important role in novelty-induced memo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371172/ https://www.ncbi.nlm.nih.gov/pubmed/25776038 http://dx.doi.org/10.1101/lm.037713.114 |
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author | Stiver, Mikaela L. Jacklin, Derek L. Mitchnick, Krista A. Vicic, Nevena Carlin, Justine O'Hara, Matthew Winters, Boyer D. |
author_facet | Stiver, Mikaela L. Jacklin, Derek L. Mitchnick, Krista A. Vicic, Nevena Carlin, Justine O'Hara, Matthew Winters, Boyer D. |
author_sort | Stiver, Mikaela L. |
collection | PubMed |
description | Consolidated memories can become destabilized and open to modification upon retrieval. Destabilization is most reliably prompted when novel information is present during memory reactivation. We hypothesized that the neurotransmitter acetylcholine (ACh) plays an important role in novelty-induced memory destabilization because of its established involvement in new learning. Accordingly, we investigated the effects of cholinergic manipulations in rats using an object recognition paradigm that requires reactivation novelty to destabilize object memories. The muscarinic receptor antagonist scopolamine, systemically or infused directly into the perirhinal cortex, blocked this novelty-induced memory destabilization. Conversely, systemic oxotremorine or carbachol, muscarinic receptor agonists, administered systemically or intraperirhinally, respectively, mimicked the destabilizing effect of novel information during reactivation. These bidirectional effects suggest a crucial influence of ACh on memory destabilization and the updating functions of reconsolidation. This is a hitherto unappreciated mnemonic role for ACh with implications for its potential involvement in cognitive flexibility and the dynamic process of long-term memory storage. |
format | Online Article Text |
id | pubmed-4371172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43711722016-04-01 Cholinergic manipulations bidirectionally regulate object memory destabilization Stiver, Mikaela L. Jacklin, Derek L. Mitchnick, Krista A. Vicic, Nevena Carlin, Justine O'Hara, Matthew Winters, Boyer D. Learn Mem Research Consolidated memories can become destabilized and open to modification upon retrieval. Destabilization is most reliably prompted when novel information is present during memory reactivation. We hypothesized that the neurotransmitter acetylcholine (ACh) plays an important role in novelty-induced memory destabilization because of its established involvement in new learning. Accordingly, we investigated the effects of cholinergic manipulations in rats using an object recognition paradigm that requires reactivation novelty to destabilize object memories. The muscarinic receptor antagonist scopolamine, systemically or infused directly into the perirhinal cortex, blocked this novelty-induced memory destabilization. Conversely, systemic oxotremorine or carbachol, muscarinic receptor agonists, administered systemically or intraperirhinally, respectively, mimicked the destabilizing effect of novel information during reactivation. These bidirectional effects suggest a crucial influence of ACh on memory destabilization and the updating functions of reconsolidation. This is a hitherto unappreciated mnemonic role for ACh with implications for its potential involvement in cognitive flexibility and the dynamic process of long-term memory storage. Cold Spring Harbor Laboratory Press 2015-04 /pmc/articles/PMC4371172/ /pubmed/25776038 http://dx.doi.org/10.1101/lm.037713.114 Text en © 2015 Stiver et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Stiver, Mikaela L. Jacklin, Derek L. Mitchnick, Krista A. Vicic, Nevena Carlin, Justine O'Hara, Matthew Winters, Boyer D. Cholinergic manipulations bidirectionally regulate object memory destabilization |
title | Cholinergic manipulations bidirectionally regulate object memory destabilization |
title_full | Cholinergic manipulations bidirectionally regulate object memory destabilization |
title_fullStr | Cholinergic manipulations bidirectionally regulate object memory destabilization |
title_full_unstemmed | Cholinergic manipulations bidirectionally regulate object memory destabilization |
title_short | Cholinergic manipulations bidirectionally regulate object memory destabilization |
title_sort | cholinergic manipulations bidirectionally regulate object memory destabilization |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371172/ https://www.ncbi.nlm.nih.gov/pubmed/25776038 http://dx.doi.org/10.1101/lm.037713.114 |
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