Comparison of HERG channel blocking effects of various β-blockers - Implication for clinical strategy

Kazunobu Kawakami, Toshihisa Nagatomo, Haruhiko Abe, Kan Kikuchi, Hiroko Takemasa, Blake D. Anson, Brian P. Delisle, Craig T. January, Yasuhide Nakashima

Research output: Contribution to journalArticlepeer-review

43 Scopus citations

Abstract

1 β-Blockers are widely used in the treatment of cardiovascular diseases. However, their effects on HERG channels at comparable conditions remain to be defined. We investigated the direct acute effects of β-blockers on HERG current and the molecular basis of drug binding to HERG channels with mutations of putative common binding site (Y652A and F656C). 2 β-Blockers were selected based on the receptor subtype. Wild-type, Y652A and F656C mutants of HERG channel were stably expressed in HEK293 cells, and the current was recorded by using whole-cell patch-clamp technique (23°C). 3 Carvedilol (nonselective), propranolol (nonselective) and ICI 118551 (β 2-selective) inhibited HERG current in a concentration- dependent manner (IC 50 0.51, 3.9 and 9.2 μM, respectively). The IC 50 value for carvedilol was a clinically relevant concentration. High metoprolol (β 1-selective) concentrations were required for blockade (IC 50 145 μM), and atenolol (β 1- selective) did not inhibit the HERG current. 4 Inhibition of HERG current by carvedilol, propranolol and ICI 118551 was partially but significantly attenuated in Y652A and F656C mutant channels. Affinities of metoprolol to Y652A and F656C mutant channels were not different compared with the wild-type. 5 HERG current block by all β-blockers was not frequency-dependent. 6 Drug affinities to HERG channels were different in β-blockers. Our results provide additional strategies for clinical usage of β-blockers. Atenolol and metoprolol may be preferable for patients with type 1 and 2 long QT syndrome. Carvedilol has a class III antiarrhythmic effect, which may provide the rationale for a favourable clinical outcome compared with other β-blockers as suggested in the recent COMET (Carvedilol Or Metoprolol European Trial) substudy.

Original languageEnglish
Pages (from-to)642-652
Number of pages11
JournalBritish Journal of Pharmacology
Volume147
Issue number6
DOIs
StatePublished - Mar 2006

Keywords

  • Arrhythmia
  • HEK293 cells
  • Heart failure
  • Ion channels
  • K channel
  • Long QT syndrome
  • Membrane currents
  • β-Blockers

ASJC Scopus subject areas

  • Pharmacology

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