Edoxaban treatment in a post-infarction experimental model

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicases_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Ciencias Morfolóxicases_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéuticaes_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psiquiatría, Radioloxía, Saúde Pública, Enfermaría e Medicinaes_ES
dc.contributor.authorMartínez-Fernández, Javier
dc.contributor.authorAlmengló Buzón, Cristina
dc.contributor.authorBabarro, Borja
dc.contributor.authorIglesias Rey, Ramón
dc.contributor.authorGarcía-Caballero Parada, Tomás
dc.contributor.authorFernández, Ángel L.
dc.contributor.authorSouto Bayarri, José Miguel
dc.contributor.authorGonzález Juanatey, José Ramón
dc.contributor.authorÁlvarez Castro, Ezequiel
dc.date.accessioned2024-03-05T09:31:54Z
dc.date.available2024-03-05T09:31:54Z
dc.date.issued2024
dc.description.abstractBackground The sequelae of myocardial infarction (MI) require specific pharmacological therapy to minimise the post-MI remodelling, which in many cases evolves into cardiovascular complications. The aim of this study was to analyse the effect of edoxaban, an oral anticoagulant, on cardiac recovery in a rat model of permanent coronary artery ligation. Methods An experimental method to assess the post-MI remodelling in rats for 4 weeks, based on cardiac magnetic resonance imaging (MRI) and final histological analysis of the hearts was performed. The influence of daily oral treatment with edoxaban (20 mg/kg/day) for 28 days post-MI was analysed in comparison to vehicle. Results In our model, edoxaban was shown to be safe and bleeding was observed in 1 of 10 animals. General physical recovery of the treated animals was shown by higher body weight recovery compared with non-treated animals (38.6 ± 2.9 vs. 29.9 ± 3.1 g, respectively, after 28 days). There was not a pronounced effect of edoxaban in post-MI cardiac remodelling, but mitigated fibrosis was observed by the reduced expression of vascular endothelial growth factor and tumour growth factor β1 in the peri-infarct zone. Conclusions Our analysis provided the experimental basis to support the feasibility of MRI to study cardiac function and characterise myocardial scarring in a rat model. Overall data suggested the safety of edoxaban in the model, and compared to placebo, it showed a better post-MI recovery, probably by reducing fibrosis of the heart. Further research on mid-term cardiac recovery with edoxaban after MI is justified.es_ES
dc.description.peerreviewedSIes_ES
dc.identifier.citationEuropean Journal of Pharmacology Volume 962, 5 January 2024, 176216es_ES
dc.identifier.doi10.1016/j.ejphar.2023.176216
dc.identifier.issn0014-2999
dc.identifier.urihttp://hdl.handle.net/10347/32986
dc.journal.titleEuropean Journal of Pharmacology
dc.language.isoenges_ES
dc.page.initial176216
dc.publisherElsevieres_ES
dc.rights© 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND licensees_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectEdoxabanes_ES
dc.subjectAcute myocardial infarction experimental modeles_ES
dc.subjectCardiac remodelling after infarctiones_ES
dc.subjectCardiac magnetic resonance imaginges_ES
dc.subjectPost-infarction anticoagulant treatmentes_ES
dc.titleEdoxaban treatment in a post-infarction experimental modeles_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dc.volume.number962
dspace.entity.typePublication
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relation.isAuthorOfPublicationd52aae38-d8dc-4796-be04-cc73866bf7d0
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relation.isAuthorOfPublication.latestForDiscoveryf825b64a-9678-43c6-8c1d-6a943ec91adb

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