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Research ArticleCHEMOTHERAPY, ANTIBIOTICS, AND GENE THERAPY

Divergent Proarrhythmic Potential of Macrolide Antibiotics Despite Similar QT Prolongation: Fast Phase 3 Repolarization Prevents Early Afterdepolarizations and Torsade de Pointes

Peter Milberg, Lars Eckardt, Hans-Jürgen Bruns, Julia Biertz, Shahram Ramtin, Nico Reinsch, Dirk Fleischer, Paulus Kirchhof, Larissa Fabritz, Günter Breithardt and Wilhelm Haverkamp
Journal of Pharmacology and Experimental Therapeutics October 2002, 303 (1) 218-225; DOI: https://doi.org/10.1124/jpet.102.037911
Peter Milberg
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Lars Eckardt
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Hans-Jürgen Bruns
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Julia Biertz
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Shahram Ramtin
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Nico Reinsch
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Dirk Fleischer
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Paulus Kirchhof
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Larissa Fabritz
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Günter Breithardt
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Wilhelm Haverkamp
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Abstract

Macrolide antibiotics are known to have a different proarrhythmic potential in the presence of comparable QT prolongation in the surface ECG. Because the extent of QT prolongation has been used as a surrogate marker for cardiotoxicity, we aimed to study the different electrophysiological effects of the macrolide antibiotics erythromycin, clarithromycin, and azithromycin in a previously developed experimental model of proarrhythmia. In 37 Langendorff-perfused rabbit hearts, erythromycin (150–300 μM, n = 13) clarithromycin (150–300 μM, n = 13), and azithromycin (150–300 μM, n = 11) led to similar increases in QT interval and monophasic action potential (MAP) duration. In bradycardic (atrioventricular-blocked) hearts, eight simultaneously recorded epi- and endocardial MAPs demonstrated increased dispersion of repolarization in the presence of all three antibiotics. Erythromycin and clarithromycin led to early afterdepolarizations (EADs) and torsade de pointes (TdP) after lowering of potassium concentration. In the presence of azithromycin, no EAD or TdP occurred. Erythromycin and clarithromycin changed the MAP configuration to a triangular pattern, whereas azithromycin caused a rectangular pattern of MAP prolongation. In 13 additional hearts, 150 μM azithromycin was administered after previous treatment with 300 μM erythromycin and suppressed TdP provoked by erythromycin. In conclusion, macrolide antibiotics lead to similar prolongation of repolarization but show a different proarrhythmic potential (erythromycin > clarithromycin > azithromycin). In the presence of azithromycin, neither EAD nor TdP occur. This effect may be related to a rectangular pattern of action potential prolongation, whereas erythromycin and clarithromycin cause triangular action potential prolongation and induce TdP.

Footnotes

  • P.M. and L.E. contributed equally to this work.

  • DOI: 10.1124/jpet.102.037911

  • Abbreviations:
    TdP
    torsade de pointes
    IKr
    rapid component of the delayed rectifier current
    AV
    atrioventricular
    MAP
    monophasic action potential
    MAP90
    monophasic action potential duration at 90% repolarization
    MAP50
    monophasic action potential duration at 50% repolarization
    EAD
    early afterdepolarization
    • Received April 26, 2002.
    • Accepted May 16, 2002.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 303 (1)
Journal of Pharmacology and Experimental Therapeutics
Vol. 303, Issue 1
1 Oct 2002
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Research ArticleCHEMOTHERAPY, ANTIBIOTICS, AND GENE THERAPY

Divergent Proarrhythmic Potential of Macrolide Antibiotics Despite Similar QT Prolongation: Fast Phase 3 Repolarization Prevents Early Afterdepolarizations and Torsade de Pointes

Peter Milberg, Lars Eckardt, Hans-Jürgen Bruns, Julia Biertz, Shahram Ramtin, Nico Reinsch, Dirk Fleischer, Paulus Kirchhof, Larissa Fabritz, Günter Breithardt and Wilhelm Haverkamp
Journal of Pharmacology and Experimental Therapeutics October 1, 2002, 303 (1) 218-225; DOI: https://doi.org/10.1124/jpet.102.037911

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Research ArticleCHEMOTHERAPY, ANTIBIOTICS, AND GENE THERAPY

Divergent Proarrhythmic Potential of Macrolide Antibiotics Despite Similar QT Prolongation: Fast Phase 3 Repolarization Prevents Early Afterdepolarizations and Torsade de Pointes

Peter Milberg, Lars Eckardt, Hans-Jürgen Bruns, Julia Biertz, Shahram Ramtin, Nico Reinsch, Dirk Fleischer, Paulus Kirchhof, Larissa Fabritz, Günter Breithardt and Wilhelm Haverkamp
Journal of Pharmacology and Experimental Therapeutics October 1, 2002, 303 (1) 218-225; DOI: https://doi.org/10.1124/jpet.102.037911
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