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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9262915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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