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Inhibition of K(Ca)2 and K(v)11.1 Channels in Pigs With Left Ventricular Dysfunction

BACKGROUND: Inhibition of K(Ca)2 channels, conducting I(KCa), can convert atrial fibrillation (AF) to sinus rhythm and protect against its induction. I(KCa) inhibition has been shown to possess functional atrial selectivity with minor effects on ventricles. Under pathophysiological conditions with v...

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Autores principales: Citerni, Carlotta, Kirchhoff, Jeppe, Olsen, Lisbeth Høier, Sattler, Stefan Michael, Grunnet, Morten, Edvardsson, Nils, Bentzen, Bo Hjorth, Diness, Jonas Goldin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219273/
https://www.ncbi.nlm.nih.gov/pubmed/32435191
http://dx.doi.org/10.3389/fphar.2020.00556
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author Citerni, Carlotta
Kirchhoff, Jeppe
Olsen, Lisbeth Høier
Sattler, Stefan Michael
Grunnet, Morten
Edvardsson, Nils
Bentzen, Bo Hjorth
Diness, Jonas Goldin
author_facet Citerni, Carlotta
Kirchhoff, Jeppe
Olsen, Lisbeth Høier
Sattler, Stefan Michael
Grunnet, Morten
Edvardsson, Nils
Bentzen, Bo Hjorth
Diness, Jonas Goldin
author_sort Citerni, Carlotta
collection PubMed
description BACKGROUND: Inhibition of K(Ca)2 channels, conducting I(KCa), can convert atrial fibrillation (AF) to sinus rhythm and protect against its induction. I(KCa) inhibition has been shown to possess functional atrial selectivity with minor effects on ventricles. Under pathophysiological conditions with ventricular remodeling, however, inhibiting I(KCa) can exhibit both proarrhythmic and antiarrhythmic ventricular effects. The aim of this study was to evaluate the effects of the I(KCa) inhibitor AP14145, when given before or after the I(Kr) blocker dofetilide, on cardiac function and ventricular proarrhythmia markers in pigs with or without left ventricular dysfunction (LVD). METHODS: Landrace pigs were randomized into an AF group (n = 6) and two control groups: SHAM1 (n = 8) and SHAM2 (n = 4). AF pigs were atrially tachypaced (A-TP) for 43 ± 4 days until sustained AF and LVD developed. A-TP and SHAM1 pigs received 20 mg/kg AP14145 followed by 100 µg/kg dofetilide whereas SHAM2 pigs received the same drugs in the opposite order. Proarrhythmic markers such as short-term variability of QT (STV(QT)) and RR (STV(RR)) intervals, and the number of premature ventricular complexes (PVCs) were measured at baseline and after administration of drugs. The influence on cardiac function was assessed by measuring cardiac output, stroke volume, and relevant echocardiographic parameters. RESULTS: I(KCa) inhibition by AP14145 did not increase STV(QT) or STV(RR) in any of the pigs. I(Kr) inhibition by dofetilide markedly increased STV(QT) in the A-TP pigs, but not in SHAM operated pigs. Upon infusion of AP14145 the number of PVCs decreased or remained unchanged both when AP14145 was infused after baseline and after dofetilide. Conversely, the number of PVCs increased or remained unchanged upon dofetilide infusion. Neither AP14145 nor dofetilide affected relevant echocardiographic parameters, cardiac output, or stroke volume in any of the groups. CONCLUSION: I(KCa) inhibition with AP14145 was not proarrhythmic in healthy pigs, or in the presence of LVD resulting from A-TP. In pigs already challenged with 100 µg/kg dofetilide there were no signs of proarrhythmia when 20 mg/kg AP14145 were infused. K(Ca)2 channel inhibition did not affect cardiac function, implying that K(Ca)2 inhibitors can be administered safely also in the presence of LV dysfunction.
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spelling pubmed-72192732020-05-20 Inhibition of K(Ca)2 and K(v)11.1 Channels in Pigs With Left Ventricular Dysfunction Citerni, Carlotta Kirchhoff, Jeppe Olsen, Lisbeth Høier Sattler, Stefan Michael Grunnet, Morten Edvardsson, Nils Bentzen, Bo Hjorth Diness, Jonas Goldin Front Pharmacol Pharmacology BACKGROUND: Inhibition of K(Ca)2 channels, conducting I(KCa), can convert atrial fibrillation (AF) to sinus rhythm and protect against its induction. I(KCa) inhibition has been shown to possess functional atrial selectivity with minor effects on ventricles. Under pathophysiological conditions with ventricular remodeling, however, inhibiting I(KCa) can exhibit both proarrhythmic and antiarrhythmic ventricular effects. The aim of this study was to evaluate the effects of the I(KCa) inhibitor AP14145, when given before or after the I(Kr) blocker dofetilide, on cardiac function and ventricular proarrhythmia markers in pigs with or without left ventricular dysfunction (LVD). METHODS: Landrace pigs were randomized into an AF group (n = 6) and two control groups: SHAM1 (n = 8) and SHAM2 (n = 4). AF pigs were atrially tachypaced (A-TP) for 43 ± 4 days until sustained AF and LVD developed. A-TP and SHAM1 pigs received 20 mg/kg AP14145 followed by 100 µg/kg dofetilide whereas SHAM2 pigs received the same drugs in the opposite order. Proarrhythmic markers such as short-term variability of QT (STV(QT)) and RR (STV(RR)) intervals, and the number of premature ventricular complexes (PVCs) were measured at baseline and after administration of drugs. The influence on cardiac function was assessed by measuring cardiac output, stroke volume, and relevant echocardiographic parameters. RESULTS: I(KCa) inhibition by AP14145 did not increase STV(QT) or STV(RR) in any of the pigs. I(Kr) inhibition by dofetilide markedly increased STV(QT) in the A-TP pigs, but not in SHAM operated pigs. Upon infusion of AP14145 the number of PVCs decreased or remained unchanged both when AP14145 was infused after baseline and after dofetilide. Conversely, the number of PVCs increased or remained unchanged upon dofetilide infusion. Neither AP14145 nor dofetilide affected relevant echocardiographic parameters, cardiac output, or stroke volume in any of the groups. CONCLUSION: I(KCa) inhibition with AP14145 was not proarrhythmic in healthy pigs, or in the presence of LVD resulting from A-TP. In pigs already challenged with 100 µg/kg dofetilide there were no signs of proarrhythmia when 20 mg/kg AP14145 were infused. K(Ca)2 channel inhibition did not affect cardiac function, implying that K(Ca)2 inhibitors can be administered safely also in the presence of LV dysfunction. Frontiers Media S.A. 2020-05-06 /pmc/articles/PMC7219273/ /pubmed/32435191 http://dx.doi.org/10.3389/fphar.2020.00556 Text en Copyright © 2020 Citerni, Kirchhoff, Olsen, Sattler, Grunnet, Edvardsson, Bentzen and Diness http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Citerni, Carlotta
Kirchhoff, Jeppe
Olsen, Lisbeth Høier
Sattler, Stefan Michael
Grunnet, Morten
Edvardsson, Nils
Bentzen, Bo Hjorth
Diness, Jonas Goldin
Inhibition of K(Ca)2 and K(v)11.1 Channels in Pigs With Left Ventricular Dysfunction
title Inhibition of K(Ca)2 and K(v)11.1 Channels in Pigs With Left Ventricular Dysfunction
title_full Inhibition of K(Ca)2 and K(v)11.1 Channels in Pigs With Left Ventricular Dysfunction
title_fullStr Inhibition of K(Ca)2 and K(v)11.1 Channels in Pigs With Left Ventricular Dysfunction
title_full_unstemmed Inhibition of K(Ca)2 and K(v)11.1 Channels in Pigs With Left Ventricular Dysfunction
title_short Inhibition of K(Ca)2 and K(v)11.1 Channels in Pigs With Left Ventricular Dysfunction
title_sort inhibition of k(ca)2 and k(v)11.1 channels in pigs with left ventricular dysfunction
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219273/
https://www.ncbi.nlm.nih.gov/pubmed/32435191
http://dx.doi.org/10.3389/fphar.2020.00556
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