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dc.creatorAidonidis I., Simopoulos V., Stravela S., Dipla K., Stamatiou R., Hatziefthimiou A., Molyvdas P.-A.en
dc.date.accessioned2023-01-31T07:30:35Z
dc.date.available2023-01-31T07:30:35Z
dc.date.issued2021
dc.identifier10.1007/s10840-020-00865-0
dc.identifier.issn1383875X
dc.identifier.urihttp://hdl.handle.net/11615/70341
dc.description.abstractPurpose: Previous clinical studies have shown that ranolazine (RAN) added to amiodarone (AMIO) might accelerate the termination of recent-onset atrial fibrillation. This study was undertaken to delineate possible mechanisms that contribute to the enhancement of the antiarrhythmic efficacy of RAN-AMIO coadministration. Methods: Ten rabbits were anesthetized and two monophasic action potential (MAP) catheters were sequentially inserted into the right atrium. One MAP electrode was used to pace and record; the other electrode was used only for recording MAP from an adjacent atrial region. Intraatrial conduction time (IACT), 2:1 intraatrial conduction block (IACB), and atrial post-repolarization refractoriness (aPRR) were consecutively determined by high-rate atrial burst pacing and programmed stimulation, respectively. All parameters were evaluated during baseline and following AMIO (3 mg/kg iv) or AMIO+RAN (2.4 mg/kg iv bolus +0.134 mg/kg/min maintenance infusion). Results: The IACT remained unchanged post AMIO compared with baseline (37.6 ± 3.8 vs 36.4 ± 2.4 ms), whereas the addition of RAN to AMIO significantly prolonged IACT (50.4 ± 3.6 ms, p <.001). The pacing cycle length producing 2:1 IACB was 101.2 ± 21.7 ms at baseline , 117.5 ± 15 ms after AMIO (p = 0.265), and 150 ± 14 ms after AMIO+RAN (p <.001). Baseline aPRR was longer following AMIO treatment (35 ± 5 vs 50 ± 9 ms, p <.01) but remarkably prolonged with RAN supplementation (105 ± 11 ms, p <.001). Conclusions: RAN significantly prolonged the propagation time of rapid atrial depolarizations and potentiated the AMIO-induced moderate increases in aPRR. These mechanisms possibly contribute to the earlier termination of atrial fibrillation when RAN is co-administered with AMIO. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.en
dc.language.isoenen
dc.sourceJournal of Interventional Cardiac Electrophysiologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85091726556&doi=10.1007%2fs10840-020-00865-0&partnerID=40&md5=9a21a27ba9a7653d50667cb16ceb6613
dc.subjectamiodaroneen
dc.subjectranolazineen
dc.subjectamiodaroneen
dc.subjectantiarrhythmic agenten
dc.subjectranolazineen
dc.subjectaction potentialen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectantiarrhythmic activityen
dc.subjectArticleen
dc.subjectatrial depolarizationen
dc.subjectatrial fibrillationen
dc.subjectcardiovascular responseen
dc.subjectcontrolled studyen
dc.subjectdrug efficacyen
dc.subjectdrug potentiationen
dc.subjectdrug responseen
dc.subjectheart atrium conductionen
dc.subjectheart atrium pacingen
dc.subjectheart beaten
dc.subjectheart depolarizationen
dc.subjectheart repolarizationen
dc.subjectnonhumanen
dc.subjectsupraventricular tachycardiaen
dc.subjectanimalen
dc.subjectatrial fibrillationen
dc.subjectheart rateen
dc.subjectLeporidaeen
dc.subjectAction Potentialsen
dc.subjectAmiodaroneen
dc.subjectAnimalsen
dc.subjectAnti-Arrhythmia Agentsen
dc.subjectAtrial Fibrillationen
dc.subjectHeart Rateen
dc.subjectRabbitsen
dc.subjectRanolazineen
dc.subjectSpringeren
dc.titleRanolazine depresses conduction of rapid atrial depolarizations in a beating rabbit heart modelen
dc.typejournalArticleen


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