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Ranolazine Prevents Levosimendan-Induced Atrial Fibrillation.
Ellermann, Christian; Kohnke, Anja; Dechering, Dirk G; Kochhäuser, Simon; Reinke, Florian; Fehr, Michael; Eckardt, Lars; Frommeyer, Gerrit.
Afiliação
  • Ellermann C; Department of Cardiology II (Electrophysiology), University Hospital Münster, Münster, Germany.
  • Kohnke A; Department of Cardiology II (Electrophysiology), University Hospital Münster, Münster, Germany.
  • Dechering DG; Department of Cardiology II (Electrophysiology), University Hospital Münster, Münster, Germany.
  • Kochhäuser S; Department of Cardiology II (Electrophysiology), University Hospital Münster, Münster, Germany.
  • Reinke F; Department of Cardiology II (Electrophysiology), University Hospital Münster, Münster, Germany.
  • Fehr M; Clinic of Exotic Pets, Reptiles, Exotic and Feral Birds, University of Hanover, Hanover, Germany.
  • Eckardt L; Department of Cardiology II (Electrophysiology), University Hospital Münster, Münster, Germany.
  • Frommeyer G; Department of Cardiology II (Electrophysiology), University Hospital Münster, Münster, Germany.
Pharmacology ; 102(3-4): 138-141, 2018.
Article em En | MEDLINE | ID: mdl-29982246
ABSTRACT

OBJECTIVES:

Levosimendan is a calcium sensitizer that is used as positive inotropic drug in acute decompensated heart failure. An increased incidence of atrial fibrillation after levosimendan-treatment was observed in clinical and experimental studies. Due to the limited range of antiarrhythmic drugs, the aim of the present study was to assess potential antiarrhythmic effects of ranolazine in levosimendan-pretreated isolated rabbit hearts.

METHODS:

Twelve rabbit hearts were excised and retrogradely perfused employing the Langendorff setup. Left and right atrial catheters were used to record monophasic action potentials and to obtain cycle length-dependent atrial action potential durations (aAPD90) and effective refractory periods (aERP). After obtaining baseline data, 0.5 µmol/L levosimendan was infused. Subsequently, 10 µmol/L ranolazine was administered.

RESULTS:

Infusion of levosimendan led to a reduction of aAPD90 (-9 ms, p < 0.05) and aERP (-13 ms, p < 0.05). Additional treatment with ranolazine prolonged aAPD90 (+23 ms, p < 0.01) and aERP (+30 ms, p < 0.05). Under baseline conditions, a predefined pacing protocol induced 77 episodes of atrial fibrillation. Infusion of levosimendan enhanced the vulnerability to atrial fibrillation (132 episodes, p = 0.14). Further treatment with ranolazine had a significant antiarrhythmic effect (61 episodes, p < 0.05).

CONCLUSIONS:

In this study, ranolazine seems to prevent atrial fibrillation in levosimendan-pretreated hearts. Underlying mechanism is a prolongation of atrial repolarization and aERP.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piridazinas / Fibrilação Atrial / Ranolazina / Hidrazonas / Antiarrítmicos Tipo de estudo: Guideline Limite: Animals Idioma: En Revista: Pharmacology Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piridazinas / Fibrilação Atrial / Ranolazina / Hidrazonas / Antiarrítmicos Tipo de estudo: Guideline Limite: Animals Idioma: En Revista: Pharmacology Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha