Volume 11 Supplement 2

17th Scientific Symposium of the Austrian Pharmacological Society (APHAR)

Open Access

Effects of diclofenac on ventricular muscle repolarization: proarrhythmic implications

  • Norbert Jost1Email author,
  • Attila Kristóf1,
  • Zsófia Kohajda1,
  • Tamás Szél1,
  • Zoltán Husti1,
  • István Koncz1,
  • Victor Juhász1,
  • István Baczkó1,
  • Julius Gy Papp1,
  • András Varró1 and
  • László Virág1
BMC Pharmacology201111(Suppl 2):A59

https://doi.org/10.1186/1471-2210-11-S2-A59

Published: 5 September 2011

Background

The aim of the present work was to characterize the electrophysiological effects of the non-steroidal anti-inflammatory drug diclofenac and to study the possible proarrhythmic potency of the drug in ventricular muscle.

Methods

Ion currents were recorded using the voltage clamp technique in canine ventricular cells, and action potentials (AP) were recorded from canine ventricular preparations using microelectrodes. The proarrhythmic potency of diclofenac was investigated in an anaesthetized rabbit proarrhythmia model.

Results

Diclofenac (30 µM) decreased the amplitude of rapid (IKr) and slow (IKs) delayed rectifier and L-type calcium currents (ICa) without influencing transient outward (Ito) and inward rectifier (IK1) potassium currents. The action potential was slightly lengthened in ventricular muscle but shortened in Purkinje fibres by diclofenac (20 µM). The maximum upstroke velocity (Vmax) was decreased in both preparations. Larger repolarization lengthening was observed when repolarization reserve was impaired by previous BaCl2 application. Diclofenac (3 mg/kg) did not prolong the QTc interval, while the potassium channel blocker dofetilide (25 µg/kg) significantly lengthened QTc in anaesthetized rabbits. The combination of diclofenac and dofetilide significantly prolonged QTc. Diclofenac alone did not induce torsades de pointes ventricular tachycardia (TdP) while TdP incidence following dofetilide was 20%. However, the combination of diclofenac and dofetilide led to a significant increase in the incidence of TdP.

Conclusions

The results indicate that diclofenac, at therapeutic concentration and even at high dose, does not increase the risk of arrhythmia in normal heart. However, high dose drug treatment may enhance the proarrhythmic risk in the heart when the repolarization reserve is reduced.

Declarations

Acknowledgements

This work was funded by grants from OTKA (CNK-77855, K-82079) and the National Development Agency (TÁMOP-4.2.1/B-09/1/KONV-2010-0005).

Authors’ Affiliations

(1)
Department of Pharmacology and Pharmacotherapy, University of Szeged; Division of Cardiovascular Pharmacology, Hungarian Academy of Sciences

Copyright

© Jost et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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