Relevance of anaesthesia for dofetilide-induced torsades de pointes in α 1-adrenoceptor-stimulated rabbits

D. Vincze, A. S. Farkas, L. Rudas, P. Makra, N. Csík, I. Leprán, T. Forster, M. Csanády, J. G. Papp, A. Varró, A. Farkas

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26 Citations (Scopus)


Background and purpose: No information is available concerning the effects of anaesthetics in the most frequently used in vivo pro-arrhythmia model. Accordingly, in this study we examined the effect of pentobarbital, propofol or α-chloralose anaesthesia on the pro-arrhythmic activity of the class III anti-arrhythmic dofetilide in α 1-adrenoceptor-stimulated rabbits. Experimental approach: Rabbits anaesthetized intravenously with pentobarbital, propofol or α-chloralose were infused simultaneously with the α 1-adrenoceptor agonist phenylephrine (15 μg kg -1 min -1, i.v.) and dofetilide (0.04 mg kg -1 min -1, i.v.). The electrocardiographic QT interval, the T peak-T end interval and certain QT variability parameters were measured. The heart rate variability and the baroreflex sensitivity were utilized to assess the vagal nerve activity. The spectral power of the systolic arterial pressure was calculated in the frequency range 0.15-0.5 Hz to assess the sympathetic activity. Key results: Pentobarbital considerably reduced, whereas propofol did not significantly affect the incidence of dofetilide-induced torsades de pointes (TdP) as compared with the results with α-chloralose (40% (P=0.011) and 70% (P=0.211) vs 100%, respectively). In additional experiments, neither doubling of the rate of the dofetilide infusion nor tripling of the rate of phenylephrine infusion elevated the incidence of TdP to the level seen with α-chloralose. None of the repolarization-related parameters predicted TdP. The indices of the parasympathetic and sympathetic activity were significantly depressed in the α-chloralose and propofol anaesthesia groups. Conclusions and implications: In rabbits, anaesthetics may affect drug-induced TdP genesis differently, which must be considered when results of different studies are compared.

Original languageEnglish
Pages (from-to)75-89
Number of pages15
JournalBritish journal of pharmacology
Issue number1
Publication statusPublished - jan. 1 2008

ASJC Scopus subject areas

  • Pharmacology

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