Electrophysiological mechanisms in a canine model of erythromycin-associated long QT syndrome

Michael Rubart, Milton L. Pressler, Harald P. Pride, Douglas P. Zipes

Research output: Contribution to journalArticle

93 Citations (Scopus)

Abstract

Background. Erythromycin is known to prolong ventricular repolarization and has been associated with the occurrence of torsades de pointes. In this study, we have investigated potential mechanisms in vivo and in vitro for induction of an acquired long QT syndrome by erythromycin. Methods and Results. Ventricular electrograms and endocardial monophasic action potentials were recorded in anesthetized open-chest dogs before and after administration of 40 to 120 mg/kg of erythromycin lactobionate. Conventional microelectrode techniques were used to record transmembrane action potentials in isolated dog Purkinje fibers and papillary muscles. Erythromycin at concentrations >20 mg/L prolonged action potential duration. At higher concentrations (100 to 200 mg/L), erythromycin induced phase 2 and phase 3 early afterdepolarizations (EADs) both in vivo and in vitro. The effects of erythromycin on repolarization were more marked in Purkinje fibers than in papillary muscle. Pretreatment of Purkinje fibers with erythromycin antagonized the effects of dofetilide, a selective delayed-rectifier potassium channel (IK) blocker. Pretreatment with prazosin or tetrodotoxin had no effect on erythromycin-induced changes in action potential duration. Conclusions. These pharmacological studies suggest that erythromycin prolongs repolarization to a large extent by block of IK. In turn, prolongation of action potential duration resulting from erythromycin's actions on IK may promote the development of EADs. The induction of ventricular arrhythmias observed clinically after exposure to erythromycin may be related to the development of EADs. The rarity of occurrence of ventricular arrhythmias suggests that other predisposing factors contribute to the acquired long QT syndrome associated with erythromycin.

Original languageEnglish (US)
Pages (from-to)1832-1844
Number of pages13
JournalCirculation
Volume88
Issue number4
DOIs
StatePublished - Oct 1993

Fingerprint

Long QT Syndrome
Erythromycin
Canidae
Action Potentials
Purkinje Fibers
Papillary Muscles
Cardiac Arrhythmias
Delayed Rectifier Potassium Channels
Potassium Channel Blockers
Dogs
Torsades de Pointes
Prazosin
Tetrodotoxin
Microelectrodes
Causality
Membrane Potentials
Thorax
Pharmacology

Keywords

  • Arrhythmia
  • Depolarizing
  • Potassium

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Electrophysiological mechanisms in a canine model of erythromycin-associated long QT syndrome. / Rubart, Michael; Pressler, Milton L.; Pride, Harald P.; Zipes, Douglas P.

In: Circulation, Vol. 88, No. 4, 10.1993, p. 1832-1844.

Research output: Contribution to journalArticle

Rubart, Michael ; Pressler, Milton L. ; Pride, Harald P. ; Zipes, Douglas P. / Electrophysiological mechanisms in a canine model of erythromycin-associated long QT syndrome. In: Circulation. 1993 ; Vol. 88, No. 4. pp. 1832-1844.
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