Edoxaban treatment in a post-infarction experimental model

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Ciencias Morfolóxicas
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psiquiatría, Radioloxía, Saúde Pública, Enfermaría e Medicina
dc.contributor.authorMartínez Fernández, Javier
dc.contributor.authorAlmengló, Cristina
dc.contributor.authorBabarro, Borja
dc.contributor.authorIglesias Rey, Ramón
dc.contributor.authorGarcía-Caballero Parada, Tomás
dc.contributor.authorFernández González, Ángel Luis
dc.contributor.authorSouto Bayarri, Miguel
dc.contributor.authorGonzález Juanatey, José Ramón
dc.contributor.authorÁlvarez Castro, Ezequiel
dc.date.accessioned2025-01-20T12:38:32Z
dc.date.available2025-01-20T12:38:32Z
dc.date.issued2023-11-29
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
dc.description.peerreviewedSI
dc.identifier.citationJavier Martínez-Fernández, Cristina Almengló, Borja Babarro, Ramón Iglesias-Rey, Tomás García-Caballero, Ángel L. Fernández, Miguel Souto-Bayarri, José R. González-Juanatey, Ezequiel Álvarez, Edoxaban treatment in a post-infarction experimental model, European Journal of Pharmacology, Volume 962, 2024, 176216, ISSN 0014-2999, https://doi.org/10.1016/j.ejphar.2023.176216
dc.identifier.doi10.1016/j.ejphar.2023.176216
dc.identifier.essn1879-0712
dc.identifier.issn0014-2999
dc.identifier.urihttps://hdl.handle.net/10347/38781
dc.journal.titleEuropean Journal of Pharmacology
dc.language.isoeng
dc.page.final10
dc.page.initial1
dc.publisherElsevier
dc.relation.publisherversionhttps://doi.org/10.1016/j.ejphar.2023.176216
dc.rights© 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/bync-nd/4.0/)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectEdoxaban
dc.subjectAcute myocardial infarction experimental model
dc.subjectCardiac remodelling after infarction
dc.subjectCardiac magnetic resonance imaging
dc.subjectPost-infarction anticoagulant treatment
dc.subject.classification32 Ciencias médicas
dc.titleEdoxaban treatment in a post-infarction experimental model
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number962
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscoveryf825b64a-9678-43c6-8c1d-6a943ec91adb

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