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Effects of dofetilide and EGIS-7229, an antiarrhythmic agent possessing class III, IV, and IB activities, on myocardial refractoriness in hyperkalemia, hypokalemia, and during beta-adrenergic activation in the rabbit papillary muscle in vitro.

Abstract
Lengthening of the effective refractory period (ERP) by EGIS-7229, a class III/Ib/IV drug, and by dofetilide, a selective I(Kr) blocker, was compared in normokalemia (NK), hypokalemia (LK), and hyperkalemia (HK) in right ventricular papillary muscles of rabbits paced at 0.5, 1, and 2 Hz, in vitro, and also during beta-adrenergic activation. In NK, EGIS-7229 (3 and 10 microM) and dofetilide (30 and 100 nM) similarly lengthened ERP in a steeply reverse frequency-dependent manner. The two compounds produced smaller ERP prolongations at 0.5 Hz in HK and LK, so rate-dependence of ERP changes decreased. EGIS-7229 lengthened ERP more at 2 Hz than at 0.5 Hz at 10 microM in LK, that is, the effect of EGIS-7229 turned into positive frequency-dependence from 3 to 10 microM. Furthermore, EGIS-7229 lengthened ERP at 10 microM more than dofetilide at 100 nM at 2 Hz stimulation rate (P<0.05). Isoproterenol (30 nM) eliminated the effect of dofetilide on ERP, while EGIS-7229 prolonged ERP during beta-adrenergic activation. In conclusion, efficacy of EGIS-7229 was superior to that of dofetilide in LK and during beta-adrenergic stimulation, suggesting improved antiarrhythmic action for EGIS-7229 under certain conditions in the patient.
AuthorsAnikó Kovács, Gábor Szénási
JournalJournal of pharmacological sciences (J Pharmacol Sci) Vol. 100 Issue 4 Pg. 303-9 (Apr 2006) ISSN: 1347-8613 [Print] Japan
PMID16603803 (Publication Type: Journal Article)
Chemical References
  • Adrenergic beta-Agonists
  • Anti-Arrhythmia Agents
  • EGIS 7229
  • Phenethylamines
  • Pyridazines
  • Sulfonamides
  • Isoproterenol
  • dofetilide
Topics
  • Adrenergic beta-Agonists (pharmacology)
  • Animals
  • Anti-Arrhythmia Agents (pharmacology)
  • Dose-Response Relationship, Drug
  • Electric Stimulation
  • Electrocardiography
  • Hyperkalemia (metabolism)
  • Hypokalemia (metabolism)
  • In Vitro Techniques
  • Isoproterenol (pharmacology)
  • Male
  • Myocardial Contraction
  • Papillary Muscles (drug effects, metabolism)
  • Phenethylamines (pharmacology)
  • Pyridazines (pharmacology)
  • Rabbits
  • Sulfonamides (pharmacology)

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