Edoxaban treatment in a post-infarction experimental model

被引:2
|
作者
Martinez-Fernandez, Javier [1 ,2 ]
Almenglo, Cristina [2 ]
Babarro, Borja [2 ]
Iglesias-Rey, Ramon [3 ]
Garcia-Caballero, Tomas [2 ,4 ,5 ]
Fernandez, Angel L. [6 ,8 ]
Souto-Bayarri, Miguel [1 ,2 ]
Gonzalez-Juanatey, Jose R. [2 ,7 ,8 ,10 ]
Alvarez, Ezequiel [2 ,8 ,9 ]
机构
[1] Complexo Hosp Univ Santiago de Compostela, Serv Radiol, Santiago De Compostela, Spain
[2] Complexo Hosp Univ Santiago de Compostela CHUS, Inst Invest Sanitaria Santiago de Compostela IDIS, SERGAS, Travesia Choupana S-N, Santiago De Compostela 15706, A Coruna, Spain
[3] Complexo Hosp Univ Santiago de Compostela CHUS, Neuroimaging & Biotechnol Lab NOBEL, Clin Neurosci Res Lab LINC, Inst Invest Sanitaria Santiago de Compostela IDIS, Santiago De Compostela 15706, A Coruna, Spain
[4] Univ Santiago de Compostela, Sch Med, Dept Morphol Sci, Santiago De Compostela 15782, Spain
[5] Univ Clin Hosp, Santiago De Compostela 15782, Spain
[6] Univ Hosp Santiago de Compostela, Heart Surg Dept, Santiago De Compostela, Spain
[7] Univ Santiago de Compostela, Dept Med, La Coruna 15782, Spain
[8] CIBERCV, Madrid, Spain
[9] Univ Santiago de Compostela, Dept Farmacol Farm & Tecnol Farmaceut, Santiago De Compostela 15782, A Coruna, Spain
[10] Complexo Hosp Univ Santiago de Compostela CHUS, Serv Cardiol, Unidad Hemodinam, SERGAS, Santiago De Compostela 15706, A Coruna, Spain
关键词
Edoxaban; Acute myocardial infarction experimental; model; Cardiac remodelling after infarction; Cardiac magnetic resonance imaging; Post-infarction anticoagulant treatment; ACUTE MYOCARDIAL-INFARCTION; VENTRICULAR-FUNCTION; HEART-FAILURE; ENHANCEMENT; CONTRAST; SIZE; ISCHEMIA; FIBROSIS; THERAPY; RATS;
D O I
10.1016/j.ejphar.2023.176216
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: 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 beta 1 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.
引用
收藏
页数:10
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