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dc.creatorAIDONIDIS I., SIMOPOULOS V., DIPLA K., HATZIEFTHIMIOU A., STAMATIOU R., SKOULARIGIS I., MOLYVDAS P.-A.en
dc.date.accessioned2023-01-31T07:30:35Z
dc.date.available2023-01-31T07:30:35Z
dc.date.issued2021
dc.identifier10.19102/ICRM.2021.120304
dc.identifier.issn21563977
dc.identifier.urihttp://hdl.handle.net/11615/70340
dc.description.abstractRanolazine (RAN) has previously been shown to lower the onset of cholinergic atrial fibrillation in intact animals; however, its efficacy in the setting of atrial tachycardia (AT) is unknown. The purpose of this study was to investigate the effects of RAN alone or in combination with amiodarone (AMIO) on rapid pacing-evoked right AT in rabbit hearts. Right atrial monophasic action potentials (MAPs) were recorded in 11 anesthetized rabbits, using combination MAP pacing catheters. Vulnerability to AT was tested by employing consecutive trains of rapid burst pacing prior to and after 2.4 mg/kg of RAN alone delivered intravenously and then in combination with 3 mg/kg of AMIO as a 15-minute infusion. Primary endpoints were postdrug AT reproducibility as well as cycle length (CL) and tachycardia duration. MAP duration at 75% repolarization and the effective refractory period (ERP) were assessed during programmed pacing to calculate the atrial postrepolarization refractoriness (aPRR = ERP - MAPD75%). AT was elicited in eight out of 11 rabbits; only these animals were included for further investigation. RAN did not abolish the inducibility of AT in any experiment; however, it prolonged its CL (baseline vs. RAN: 120 ± 16 ms vs. 138 ± 18 ms; p = 0.053). Supplemental AMIO further increased the AT CL (baseline vs. RAN + AMIO: 120 ± 16 ms vs. 152 ± 23 ms; p = 0.006), without affecting arrhythmia reinducibility. Slowing of the tachycardia after RAN or RAN + AMIO was associated with spontaneous termination of the arrhythmia. RAN prolonged the aPRR significantly, while AMIO in addition to RAN potentiated this effect. Neither RAN alone nor its combination with AMIO abolished the elicitation of AT in this model. However, both agents synergistically prolonged the aPRR, resulting in the slowing of AT and promoting spontaneous termination of the arrhythmia. © 2021 Jurnal Ilmu Sosial dan Ilmu Politik. All rights reserved.en
dc.language.isoenen
dc.sourceJournal of Innovations in Cardiac Rhythm Managementen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85104554532&doi=10.19102%2fICRM.2021.120304&partnerID=40&md5=0b2c7598a2f16c1d19f3520483818ae7
dc.subjectamiodaroneen
dc.subjectranolazineen
dc.subjectaction potentialen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectanimal tissueen
dc.subjectArticleen
dc.subjectcontrolled studyen
dc.subjectdisease durationen
dc.subjectdrug effecten
dc.subjectdrug efficacyen
dc.subjecteffective refractory perioden
dc.subjectfemaleen
dc.subjectheart atrium conductionen
dc.subjectheart atrium pacingen
dc.subjectheart electrophysiologyen
dc.subjectheart repolarizationen
dc.subjectmaleen
dc.subjectnonhumanen
dc.subjectpacemaker mediated tachycardiaen
dc.subjectpolypharmacyen
dc.subjectreentry tachycardiaen
dc.subjectrefractory perioden
dc.subjectreproducibilityen
dc.subjectsupraventricular tachycardiaen
dc.subjectMediaSphere Medical LLCen
dc.titleEffects of ranolazine and its combination with amiodarone on rapid pacing-induced reentrant atrial tachycardia in rabbitsen
dc.typejournalArticleen


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