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Hippocampal inactivation during rearing on hind legs impairs spatial memory

Spatial memory requires an intact hippocampus. Hippocampal function during epochs of locomotion and quiet rest (e.g., grooming and reward consumption) has been the target of extensive study. However, during navigation rats frequently rear up onto their hind legs, and the importance of hippocampal ac...

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Autores principales: Layfield, Dylan, Sidell, Nathan, Blankenberger, Kevin, Newman, Ehren Lee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105745/
https://www.ncbi.nlm.nih.gov/pubmed/37061540
http://dx.doi.org/10.1038/s41598-023-33209-9
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author Layfield, Dylan
Sidell, Nathan
Blankenberger, Kevin
Newman, Ehren Lee
author_facet Layfield, Dylan
Sidell, Nathan
Blankenberger, Kevin
Newman, Ehren Lee
author_sort Layfield, Dylan
collection PubMed
description Spatial memory requires an intact hippocampus. Hippocampal function during epochs of locomotion and quiet rest (e.g., grooming and reward consumption) has been the target of extensive study. However, during navigation rats frequently rear up onto their hind legs, and the importance of hippocampal activity during these periods of attentive sampling for spatial memory is unknown. To address this, we tested the necessity of dorsal hippocampal activity during rearing epochs in the study phase of a delayed win-shift task for memory performance in the subsequent test phase. Hippocampal activity was manipulated with closed-loop, bilateral, optogenetic inactivation. Spatial memory accuracy was significantly and selectively reduced when the dorsal hippocampus was inactivated during rearing epochs at encoding. These data show that hippocampal activity during periods of rearing can be important for spatial memory, revealing a novel link between hippocampal function during epochs of rearing and spatial memory.
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spelling pubmed-101057452023-04-17 Hippocampal inactivation during rearing on hind legs impairs spatial memory Layfield, Dylan Sidell, Nathan Blankenberger, Kevin Newman, Ehren Lee Sci Rep Article Spatial memory requires an intact hippocampus. Hippocampal function during epochs of locomotion and quiet rest (e.g., grooming and reward consumption) has been the target of extensive study. However, during navigation rats frequently rear up onto their hind legs, and the importance of hippocampal activity during these periods of attentive sampling for spatial memory is unknown. To address this, we tested the necessity of dorsal hippocampal activity during rearing epochs in the study phase of a delayed win-shift task for memory performance in the subsequent test phase. Hippocampal activity was manipulated with closed-loop, bilateral, optogenetic inactivation. Spatial memory accuracy was significantly and selectively reduced when the dorsal hippocampus was inactivated during rearing epochs at encoding. These data show that hippocampal activity during periods of rearing can be important for spatial memory, revealing a novel link between hippocampal function during epochs of rearing and spatial memory. Nature Publishing Group UK 2023-04-15 /pmc/articles/PMC10105745/ /pubmed/37061540 http://dx.doi.org/10.1038/s41598-023-33209-9 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Layfield, Dylan
Sidell, Nathan
Blankenberger, Kevin
Newman, Ehren Lee
Hippocampal inactivation during rearing on hind legs impairs spatial memory
title Hippocampal inactivation during rearing on hind legs impairs spatial memory
title_full Hippocampal inactivation during rearing on hind legs impairs spatial memory
title_fullStr Hippocampal inactivation during rearing on hind legs impairs spatial memory
title_full_unstemmed Hippocampal inactivation during rearing on hind legs impairs spatial memory
title_short Hippocampal inactivation during rearing on hind legs impairs spatial memory
title_sort hippocampal inactivation during rearing on hind legs impairs spatial memory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105745/
https://www.ncbi.nlm.nih.gov/pubmed/37061540
http://dx.doi.org/10.1038/s41598-023-33209-9
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