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dc.contributor.authorSenserrich Guerrero, Julia
dc.contributor.authorCastro Fernández, María Elena 
dc.contributor.authorFlorensa Zanuy, Eva Ariadna 
dc.contributor.authorDíaz Martínez, Álvaro Marcelino
dc.contributor.authorPazos Carro, Ángel 
dc.contributor.authorAdell Calduch, Albert
dc.contributor.authorTzinia, Athina
dc.contributor.authorPilar Cuéllar, María Fuencisla 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-09-26T08:47:44Z
dc.date.available2025-09-26T08:47:44Z
dc.date.issued2025
dc.identifier.issn2042-6410
dc.identifier.otherRTI2018-097534-B-I00
dc.identifier.otherRED2022-134191-T
dc.identifier.urihttps://hdl.handle.net/10902/37474
dc.description.abstractBackground: Major depressive disorder is one of the main causes of disability worldwide, but its etiopathology remains largely unknown, although several hypotheses have been proposed. Recent studies suggest a potential role for matrix metalloproteinase 9 (MMP-9) in depression, as it is overexpressed in the plasma of depressed patients and normalizes following chronic antidepressant treatment. This study aimed to characterize anxiety and depression-like behaviors in transgenic MMP-9 mice, as well as the expression of different neuroplasticity markers associated with depression, in both sexes. Methods: In this study, we characterized the behavioral phenotypes of both MMP-9 knockout and MMP-9-overexpressing male and female mice. Here, we used a battery of tests to assess anxiety (open field, light?dark box, elevated plus maze, and novelty?suppressed feeding tests), depressive-like (tail suspension and social interaction tests), and cognitive (T-maze) behaviors. Results: MMP-9 knockout female mice displayed increased innate anxiety (open field test), decreased behavioral despair (tail suspension test). Compared with control mice, female MMP-9 knockout mice presented increased levels of different neuroplasticity markers in the hippocampus. With respect to MMP-9-overexpressing mice, females presented decreased innate anxiety (elevated plus maze). Male MMP-9-overexpressing mice presented greater conflict-based anxiety (novelty-suppressed feeding test) than control mice did. Conclusions: MMP-9 activity modifies anxiety- and depression-like behaviors, as well as neuroplasticity markers, in female but not in male mice. These findings reinforce the sex differences in the etiopathology of depressioes_ES
dc.description.sponsorshipThis research was funded by the Ministerio de Ciencia, Innovación y Universidades (RTI2018-097534-B-I00), Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), the Instituto de Salud Carlos III (FIS Grant PI19-00170), which were co-funded by the European Regional Development Fund (‘A way to build Europe’), and the Spanish Network for Stress Research RED2022-134191-T financed by MCIN/AEI/10.13039/501100011033.es_ES
dc.format.extent16 p.es_ES
dc.language.isoenges_ES
dc.rights© The Author(s) 2025. This article is licensed under a Creative Commons Attribution 4.0 International License.es_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceBiology of Sex Differences, 2025, 16(1), 34es_ES
dc.subject.otherDepressiones_ES
dc.subject.otherAnxietyes_ES
dc.subject.otherMatrix metalloproteinase-9Transgenic micees_ES
dc.subject.otherSexes_ES
dc.subject.otherNeuroplasticityes_ES
dc.titleSex differences in the modulation of anxiety- and depression-like behaviors by matrix metalloproteinase-9 expression levels in mice.es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1186/s13293-025-00716-5es_ES
dc.rights.accessRightsopenAccesses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-097534-B-I00/ES/METALOPROTEINASA-9 Y DEPRESION: ESTUDIO EN UN MODELO ANIMAL Y EN MUESTRAS CEREBRALES HUMANAS POSTMORTEN, Y PAPEL EN EL MECANISMO DE ACCION DE ANTIDEPRESIVOS DE ACCION RAPIDA/es_ES
dc.identifier.DOI10.1186/s13293-025-00716-5
dc.type.versionpublishedVersiones_ES


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© The Author(s) 2025. This article is licensed under a Creative Commons Attribution 4.0 International License.Excepto si se señala otra cosa, la licencia del ítem se describe como © The Author(s) 2025. This article is licensed under a Creative Commons Attribution 4.0 International License.