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Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition
Acetylcholine (ACh), released in the hippocampus from fibers originating in the medial septum/diagonal band of Broca (MSDB) complex, is crucial for learning and memory. The CA2 region of the hippocampus has received increasing attention in the context of social memory. However, the contribution of A...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547952/ https://www.ncbi.nlm.nih.gov/pubmed/34696824 http://dx.doi.org/10.7554/eLife.65580 |
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author | Pimpinella, Domenico Mastrorilli, Valentina Giorgi, Corinna Coemans, Silke Lecca, Salvatore Lalive, Arnaud L Ostermann, Hannah Fuchs, Elke C Monyer, Hannah Mele, Andrea Cherubini, Enrico Griguoli, Marilena |
author_facet | Pimpinella, Domenico Mastrorilli, Valentina Giorgi, Corinna Coemans, Silke Lecca, Salvatore Lalive, Arnaud L Ostermann, Hannah Fuchs, Elke C Monyer, Hannah Mele, Andrea Cherubini, Enrico Griguoli, Marilena |
author_sort | Pimpinella, Domenico |
collection | PubMed |
description | Acetylcholine (ACh), released in the hippocampus from fibers originating in the medial septum/diagonal band of Broca (MSDB) complex, is crucial for learning and memory. The CA2 region of the hippocampus has received increasing attention in the context of social memory. However, the contribution of ACh to this process remains unclear. Here, we show that in mice, ACh controls social memory. Specifically, MSDB cholinergic neurons inhibition impairs social novelty discrimination, meaning the propensity of a mouse to interact with a novel rather than a familiar conspecific. This effect is mimicked by a selective antagonist of nicotinic AChRs delivered in CA2. Ex vivo recordings from hippocampal slices provide insight into the underlying mechanism, as activation of nAChRs by nicotine increases the excitatory drive to CA2 principal cells via disinhibition. In line with this observation, optogenetic activation of cholinergic neurons in MSDB increases the firing of CA2 principal cells in vivo. These results point to nAChRs as essential players in social novelty discrimination by controlling inhibition in the CA2 region. |
format | Online Article Text |
id | pubmed-8547952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-85479522021-10-27 Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition Pimpinella, Domenico Mastrorilli, Valentina Giorgi, Corinna Coemans, Silke Lecca, Salvatore Lalive, Arnaud L Ostermann, Hannah Fuchs, Elke C Monyer, Hannah Mele, Andrea Cherubini, Enrico Griguoli, Marilena eLife Neuroscience Acetylcholine (ACh), released in the hippocampus from fibers originating in the medial septum/diagonal band of Broca (MSDB) complex, is crucial for learning and memory. The CA2 region of the hippocampus has received increasing attention in the context of social memory. However, the contribution of ACh to this process remains unclear. Here, we show that in mice, ACh controls social memory. Specifically, MSDB cholinergic neurons inhibition impairs social novelty discrimination, meaning the propensity of a mouse to interact with a novel rather than a familiar conspecific. This effect is mimicked by a selective antagonist of nicotinic AChRs delivered in CA2. Ex vivo recordings from hippocampal slices provide insight into the underlying mechanism, as activation of nAChRs by nicotine increases the excitatory drive to CA2 principal cells via disinhibition. In line with this observation, optogenetic activation of cholinergic neurons in MSDB increases the firing of CA2 principal cells in vivo. These results point to nAChRs as essential players in social novelty discrimination by controlling inhibition in the CA2 region. eLife Sciences Publications, Ltd 2021-10-26 /pmc/articles/PMC8547952/ /pubmed/34696824 http://dx.doi.org/10.7554/eLife.65580 Text en © 2021, Pimpinella et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Pimpinella, Domenico Mastrorilli, Valentina Giorgi, Corinna Coemans, Silke Lecca, Salvatore Lalive, Arnaud L Ostermann, Hannah Fuchs, Elke C Monyer, Hannah Mele, Andrea Cherubini, Enrico Griguoli, Marilena Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition |
title | Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition |
title_full | Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition |
title_fullStr | Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition |
title_full_unstemmed | Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition |
title_short | Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition |
title_sort | septal cholinergic input to ca2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547952/ https://www.ncbi.nlm.nih.gov/pubmed/34696824 http://dx.doi.org/10.7554/eLife.65580 |
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