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Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses

BACKGROUND: Antiarrhythmic compounds against atrial fibrillation (AF) often have reduced efficacy and may display cardiac and/or noncardiac toxicity. Efficacy can be improved by combining 2 compounds with distinct mechanisms, and it may be possible to use lower doses of each compound, thereby reduci...

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Autores principales: Carstensen, Helena, Kjær, Line, Haugaard, Maria Mathilde, Flethøj, Mette, Hesselkilde, Eva Zander, Kanters, Jørgen K., Pehrson, Steen, Buhl, Rikke, Jespersen, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of Cardiovascular Pharmacology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768216/
https://www.ncbi.nlm.nih.gov/pubmed/29068807
http://dx.doi.org/10.1097/FJC.0000000000000541
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author Carstensen, Helena
Kjær, Line
Haugaard, Maria Mathilde
Flethøj, Mette
Hesselkilde, Eva Zander
Kanters, Jørgen K.
Pehrson, Steen
Buhl, Rikke
Jespersen, Thomas
author_facet Carstensen, Helena
Kjær, Line
Haugaard, Maria Mathilde
Flethøj, Mette
Hesselkilde, Eva Zander
Kanters, Jørgen K.
Pehrson, Steen
Buhl, Rikke
Jespersen, Thomas
author_sort Carstensen, Helena
collection PubMed
description BACKGROUND: Antiarrhythmic compounds against atrial fibrillation (AF) often have reduced efficacy and may display cardiac and/or noncardiac toxicity. Efficacy can be improved by combining 2 compounds with distinct mechanisms, and it may be possible to use lower doses of each compound, thereby reducing the likelihood of adverse side effects. The purpose of this study was to investigate whether the effective doses of dofetilide and ranolazine can be reduced if the drugs are combined. METHODS: Dofetilide, ranolazine, and a combination of these were administered in 4 incremental dosing regimens to horses with acutely pacing-induced AF. Time to cardioversion, atrial effective refractory period, and AF vulnerability and duration were assessed. RESULTS: Of 8 horses, 6 cardioverted to sinus rhythm after infusion with a combination of 0.889 μg/kg dofetilide and 0.104 mg/kg ranolazine. Two horses cardioverted with 0.104 mg/kg ranolazine alone, and 3 cardioverted with 0.889 μg/kg dofetilide alone. The combination therapy decreased AF vulnerability (P < 0.05) and AF duration (P < 0.05). No change in atrial effective refractory period was detected with any of the drugs. CONCLUSIONS: The combination of dofetilide and ranolazine showed increased antiarrhythmic effects on acutely induced AF in horses, affecting time to cardioversion, AF vulnerability, and AF duration.
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spelling pubmed-57682162018-02-02 Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses Carstensen, Helena Kjær, Line Haugaard, Maria Mathilde Flethøj, Mette Hesselkilde, Eva Zander Kanters, Jørgen K. Pehrson, Steen Buhl, Rikke Jespersen, Thomas J Cardiovasc Pharmacol Original Article BACKGROUND: Antiarrhythmic compounds against atrial fibrillation (AF) often have reduced efficacy and may display cardiac and/or noncardiac toxicity. Efficacy can be improved by combining 2 compounds with distinct mechanisms, and it may be possible to use lower doses of each compound, thereby reducing the likelihood of adverse side effects. The purpose of this study was to investigate whether the effective doses of dofetilide and ranolazine can be reduced if the drugs are combined. METHODS: Dofetilide, ranolazine, and a combination of these were administered in 4 incremental dosing regimens to horses with acutely pacing-induced AF. Time to cardioversion, atrial effective refractory period, and AF vulnerability and duration were assessed. RESULTS: Of 8 horses, 6 cardioverted to sinus rhythm after infusion with a combination of 0.889 μg/kg dofetilide and 0.104 mg/kg ranolazine. Two horses cardioverted with 0.104 mg/kg ranolazine alone, and 3 cardioverted with 0.889 μg/kg dofetilide alone. The combination therapy decreased AF vulnerability (P < 0.05) and AF duration (P < 0.05). No change in atrial effective refractory period was detected with any of the drugs. CONCLUSIONS: The combination of dofetilide and ranolazine showed increased antiarrhythmic effects on acutely induced AF in horses, affecting time to cardioversion, AF vulnerability, and AF duration. Journal of Cardiovascular Pharmacology 2018-01 2017-10-25 /pmc/articles/PMC5768216/ /pubmed/29068807 http://dx.doi.org/10.1097/FJC.0000000000000541 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Article
Carstensen, Helena
Kjær, Line
Haugaard, Maria Mathilde
Flethøj, Mette
Hesselkilde, Eva Zander
Kanters, Jørgen K.
Pehrson, Steen
Buhl, Rikke
Jespersen, Thomas
Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses
title Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses
title_full Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses
title_fullStr Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses
title_full_unstemmed Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses
title_short Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses
title_sort antiarrhythmic effects of combining dofetilide and ranolazine in a model of acutely induced atrial fibrillation in horses
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768216/
https://www.ncbi.nlm.nih.gov/pubmed/29068807
http://dx.doi.org/10.1097/FJC.0000000000000541
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