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Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus

Cognitive function relies on a balanced interplay between excitatory and inhibitory neurons (INs), but the impact of estradiol on IN function is not fully understood. Here, we characterize the regulation of hippocampal INs by aromatase, the enzyme responsible for estradiol synthesis, using a combina...

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Autores principales: Hernández-Vivanco, Alicia, Cano-Adamuz, Nuria, Sánchez-Aguilera, Alberto, González-Alonso, Alba, Rodríguez-Fernández, Alberto, Azcoitia, Íñigo, de la Prida, Liset Menendez, Méndez, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262915/
https://www.ncbi.nlm.nih.gov/pubmed/35798748
http://dx.doi.org/10.1038/s41467-022-31635-3
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author Hernández-Vivanco, Alicia
Cano-Adamuz, Nuria
Sánchez-Aguilera, Alberto
González-Alonso, Alba
Rodríguez-Fernández, Alberto
Azcoitia, Íñigo
de la Prida, Liset Menendez
Méndez, Pablo
author_facet Hernández-Vivanco, Alicia
Cano-Adamuz, Nuria
Sánchez-Aguilera, Alberto
González-Alonso, Alba
Rodríguez-Fernández, Alberto
Azcoitia, Íñigo
de la Prida, Liset Menendez
Méndez, Pablo
author_sort Hernández-Vivanco, Alicia
collection PubMed
description Cognitive function relies on a balanced interplay between excitatory and inhibitory neurons (INs), but the impact of estradiol on IN function is not fully understood. Here, we characterize the regulation of hippocampal INs by aromatase, the enzyme responsible for estradiol synthesis, using a combination of molecular, genetic, functional and behavioral tools. The results show that CA1 parvalbumin-expressing INs (PV-INs) contribute to brain estradiol synthesis. Brain aromatase regulates synaptic inhibition through a mechanism that involves modification of perineuronal nets enwrapping PV-INs. In the female brain, aromatase modulates PV-INs activity, the dynamics of network oscillations and hippocampal-dependent memory. Aromatase regulation of PV-INs and inhibitory synapses is determined by the gonads and independent of sex chromosomes. These results suggest PV-INs are mediators of estrogenic regulation of behaviorally-relevant activity.
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spelling pubmed-92629152022-07-09 Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus Hernández-Vivanco, Alicia Cano-Adamuz, Nuria Sánchez-Aguilera, Alberto González-Alonso, Alba Rodríguez-Fernández, Alberto Azcoitia, Íñigo de la Prida, Liset Menendez Méndez, Pablo Nat Commun Article Cognitive function relies on a balanced interplay between excitatory and inhibitory neurons (INs), but the impact of estradiol on IN function is not fully understood. Here, we characterize the regulation of hippocampal INs by aromatase, the enzyme responsible for estradiol synthesis, using a combination of molecular, genetic, functional and behavioral tools. The results show that CA1 parvalbumin-expressing INs (PV-INs) contribute to brain estradiol synthesis. Brain aromatase regulates synaptic inhibition through a mechanism that involves modification of perineuronal nets enwrapping PV-INs. In the female brain, aromatase modulates PV-INs activity, the dynamics of network oscillations and hippocampal-dependent memory. Aromatase regulation of PV-INs and inhibitory synapses is determined by the gonads and independent of sex chromosomes. These results suggest PV-INs are mediators of estrogenic regulation of behaviorally-relevant activity. Nature Publishing Group UK 2022-07-07 /pmc/articles/PMC9262915/ /pubmed/35798748 http://dx.doi.org/10.1038/s41467-022-31635-3 Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hernández-Vivanco, Alicia
Cano-Adamuz, Nuria
Sánchez-Aguilera, Alberto
González-Alonso, Alba
Rodríguez-Fernández, Alberto
Azcoitia, Íñigo
de la Prida, Liset Menendez
Méndez, Pablo
Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus
title Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus
title_full Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus
title_fullStr Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus
title_full_unstemmed Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus
title_short Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus
title_sort sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262915/
https://www.ncbi.nlm.nih.gov/pubmed/35798748
http://dx.doi.org/10.1038/s41467-022-31635-3
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