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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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