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Ventral hippocampus-lateral septum circuitry promotes foraging-related memory
Remembering the location of a food or water source is essential for survival. Here, we reveal that spatial memory for food location is reflected in ventral hippocampus (HPCv) neuron activity and is impaired by HPCv lesion. HPCv mediation of foraging-related memory involves communication to the later...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605732/ https://www.ncbi.nlm.nih.gov/pubmed/36170832 http://dx.doi.org/10.1016/j.celrep.2022.111402 |
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author | Décarie-Spain, Léa Liu, Clarissa M. Lauer, Logan Tierno Subramanian, Keshav Bashaw, Alexander G. Klug, Molly E. Gianatiempo, Isabella H. Suarez, Andrea N. Noble, Emily E. Donohue, Kristen N. Cortella, Alyssa M. Hahn, Joel D. Davis, Elizabeth A. Kanoski, Scott E. |
author_facet | Décarie-Spain, Léa Liu, Clarissa M. Lauer, Logan Tierno Subramanian, Keshav Bashaw, Alexander G. Klug, Molly E. Gianatiempo, Isabella H. Suarez, Andrea N. Noble, Emily E. Donohue, Kristen N. Cortella, Alyssa M. Hahn, Joel D. Davis, Elizabeth A. Kanoski, Scott E. |
author_sort | Décarie-Spain, Léa |
collection | PubMed |
description | Remembering the location of a food or water source is essential for survival. Here, we reveal that spatial memory for food location is reflected in ventral hippocampus (HPCv) neuron activity and is impaired by HPCv lesion. HPCv mediation of foraging-related memory involves communication to the lateral septum (LS), as either reversible or chronic disconnection of HPCv-to-LS signaling impairs spatial memory retention for food or water location. This neural pathway selectively encodes appetitive spatial memory, as HPCv-LS disconnection does not affect spatial memory for escape location in a negative reinforcement procedure, food intake, or social and olfactory-based appetitive learning. Neural pathway tracing and functional mapping analyses reveal that LS neurons recruited during the appetitive spatial memory procedure are primarily GABAergic neurons that project to the lateral hypothalamus. Collective results emphasize that the neural substrates controlling spatial memory are outcome specific based on reinforcer modality. |
format | Online Article Text |
id | pubmed-9605732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-96057322022-10-26 Ventral hippocampus-lateral septum circuitry promotes foraging-related memory Décarie-Spain, Léa Liu, Clarissa M. Lauer, Logan Tierno Subramanian, Keshav Bashaw, Alexander G. Klug, Molly E. Gianatiempo, Isabella H. Suarez, Andrea N. Noble, Emily E. Donohue, Kristen N. Cortella, Alyssa M. Hahn, Joel D. Davis, Elizabeth A. Kanoski, Scott E. Cell Rep Article Remembering the location of a food or water source is essential for survival. Here, we reveal that spatial memory for food location is reflected in ventral hippocampus (HPCv) neuron activity and is impaired by HPCv lesion. HPCv mediation of foraging-related memory involves communication to the lateral septum (LS), as either reversible or chronic disconnection of HPCv-to-LS signaling impairs spatial memory retention for food or water location. This neural pathway selectively encodes appetitive spatial memory, as HPCv-LS disconnection does not affect spatial memory for escape location in a negative reinforcement procedure, food intake, or social and olfactory-based appetitive learning. Neural pathway tracing and functional mapping analyses reveal that LS neurons recruited during the appetitive spatial memory procedure are primarily GABAergic neurons that project to the lateral hypothalamus. Collective results emphasize that the neural substrates controlling spatial memory are outcome specific based on reinforcer modality. 2022-09-27 /pmc/articles/PMC9605732/ /pubmed/36170832 http://dx.doi.org/10.1016/j.celrep.2022.111402 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Décarie-Spain, Léa Liu, Clarissa M. Lauer, Logan Tierno Subramanian, Keshav Bashaw, Alexander G. Klug, Molly E. Gianatiempo, Isabella H. Suarez, Andrea N. Noble, Emily E. Donohue, Kristen N. Cortella, Alyssa M. Hahn, Joel D. Davis, Elizabeth A. Kanoski, Scott E. Ventral hippocampus-lateral septum circuitry promotes foraging-related memory |
title | Ventral hippocampus-lateral septum circuitry promotes foraging-related memory |
title_full | Ventral hippocampus-lateral septum circuitry promotes foraging-related memory |
title_fullStr | Ventral hippocampus-lateral septum circuitry promotes foraging-related memory |
title_full_unstemmed | Ventral hippocampus-lateral septum circuitry promotes foraging-related memory |
title_short | Ventral hippocampus-lateral septum circuitry promotes foraging-related memory |
title_sort | ventral hippocampus-lateral septum circuitry promotes foraging-related memory |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605732/ https://www.ncbi.nlm.nih.gov/pubmed/36170832 http://dx.doi.org/10.1016/j.celrep.2022.111402 |
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