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Developmental onset distinguishes three types of spontaneous recognition memory in mice
Spontaneous recognition memory tasks build on an animal’s natural preference for novelty to assess the what, where and when components of episodic memory. Their simplicity, ethological relevance and cross-species adaptability make them extremely useful to study the physiology and pathology of memory...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326931/ https://www.ncbi.nlm.nih.gov/pubmed/32606443 http://dx.doi.org/10.1038/s41598-020-67619-w |
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author | Cruz-Sanchez, Arely Dematagoda, Shadini Ahmed, Ridda Mohanathaas, Sakhithya Odenwald, Nicole Arruda-Carvalho, Maithe |
author_facet | Cruz-Sanchez, Arely Dematagoda, Shadini Ahmed, Ridda Mohanathaas, Sakhithya Odenwald, Nicole Arruda-Carvalho, Maithe |
author_sort | Cruz-Sanchez, Arely |
collection | PubMed |
description | Spontaneous recognition memory tasks build on an animal’s natural preference for novelty to assess the what, where and when components of episodic memory. Their simplicity, ethological relevance and cross-species adaptability make them extremely useful to study the physiology and pathology of memory. Recognition memory deficits are common in rodent models of neurodevelopmental disorders, and yet very little is known about the expression of spontaneous recognition memory in young rodents. This is exacerbated by the paucity of data on the developmental onset of recognition memory in mice, a major animal model of disease. To address this, we characterized the ontogeny of three types of spontaneous recognition memory in mice: object location, novel object recognition and temporal order recognition. We found that object location is the first to emerge, at postnatal day (P)21. This was followed by novel object recognition (24 h delay), at P25. Temporal order recognition was the last to emerge, at P28. Elucidating the developmental expression of recognition memory in mice is critical to improving our understanding of the ontogeny of episodic memory, and establishes a necessary blueprint to apply these tasks to probe cognitive deficits at clinically relevant time points in animal models of developmental disorders. |
format | Online Article Text |
id | pubmed-7326931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73269312020-07-01 Developmental onset distinguishes three types of spontaneous recognition memory in mice Cruz-Sanchez, Arely Dematagoda, Shadini Ahmed, Ridda Mohanathaas, Sakhithya Odenwald, Nicole Arruda-Carvalho, Maithe Sci Rep Article Spontaneous recognition memory tasks build on an animal’s natural preference for novelty to assess the what, where and when components of episodic memory. Their simplicity, ethological relevance and cross-species adaptability make them extremely useful to study the physiology and pathology of memory. Recognition memory deficits are common in rodent models of neurodevelopmental disorders, and yet very little is known about the expression of spontaneous recognition memory in young rodents. This is exacerbated by the paucity of data on the developmental onset of recognition memory in mice, a major animal model of disease. To address this, we characterized the ontogeny of three types of spontaneous recognition memory in mice: object location, novel object recognition and temporal order recognition. We found that object location is the first to emerge, at postnatal day (P)21. This was followed by novel object recognition (24 h delay), at P25. Temporal order recognition was the last to emerge, at P28. Elucidating the developmental expression of recognition memory in mice is critical to improving our understanding of the ontogeny of episodic memory, and establishes a necessary blueprint to apply these tasks to probe cognitive deficits at clinically relevant time points in animal models of developmental disorders. Nature Publishing Group UK 2020-06-30 /pmc/articles/PMC7326931/ /pubmed/32606443 http://dx.doi.org/10.1038/s41598-020-67619-w 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 Cruz-Sanchez, Arely Dematagoda, Shadini Ahmed, Ridda Mohanathaas, Sakhithya Odenwald, Nicole Arruda-Carvalho, Maithe Developmental onset distinguishes three types of spontaneous recognition memory in mice |
title | Developmental onset distinguishes three types of spontaneous recognition memory in mice |
title_full | Developmental onset distinguishes three types of spontaneous recognition memory in mice |
title_fullStr | Developmental onset distinguishes three types of spontaneous recognition memory in mice |
title_full_unstemmed | Developmental onset distinguishes three types of spontaneous recognition memory in mice |
title_short | Developmental onset distinguishes three types of spontaneous recognition memory in mice |
title_sort | developmental onset distinguishes three types of spontaneous recognition memory in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326931/ https://www.ncbi.nlm.nih.gov/pubmed/32606443 http://dx.doi.org/10.1038/s41598-020-67619-w |
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