Effect of beta-adrenoceptor blockers on human ether-a-go-go-related gene (HERG) potassium channels

Basic Clin Pharmacol Toxicol. 2005 Feb;96(2):123-30. doi: 10.1111/j.1742-7843.2005.pto960206.x.

Abstract

Patients with congenital long QT syndrome may develop arrhythmias under conditions of increased sympathetic tone. We have addressed whether some of the beta-adrenoceptor blockers commonly used to prevent the development of these arrhythmias could per se block the cardiac HERG (Human Ether-a-go-go-Related Gene) potassium channels, which would be a most unwanted side effect. HERG potassium channels were heterologously expressed in Xenopus oocytes and the currents measured by two-electrode-voltage-clamp technique. Propranolol caused a concentration-dependent inhibition of HERG current with an IC50 value of 81 microM at -10 mV. When HERG was co-expressed with the accessory subunit KCNE2, an IC50 value of 52 microM was determined. The block by propranolol was voltage-dependent, but it did not change the HERG channel deactivation kinetics. The propranolol analogue ICI118551 ((+/-)-1-[2,3-(dihydro-7-methyl-1H-inden-4-yl)oxy]-3-[(1-methylethyl)amino]-2-butanol hydrochloride) blocked the HERG channel with similar affinity, whereas the beta1-receptor antagonists metoprolol and atenolol showed weak effects. Further, the four compounds blocked HERG channels expressed in a mammalian HEK293 cell line. These data showed that HERG blockade by beta-adrenoceptor blockers occurred only at high micromolar concentrations, which are significantly above the recently established safe margin of 100 (Redfern et al., 2003).

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Adrenergic beta-Antagonists / chemistry
  • Adrenergic beta-Antagonists / pharmacology*
  • Animals
  • Cell Line
  • Dose-Response Relationship, Drug
  • Electrophysiology
  • Gene Expression / genetics
  • Humans
  • Inhibitory Concentration 50
  • Metoprolol / pharmacology
  • Oocytes / drug effects
  • Oocytes / physiology
  • Patch-Clamp Techniques
  • Potassium Channels, Voltage-Gated / drug effects*
  • Potassium Channels, Voltage-Gated / genetics*
  • Propanolamines / pharmacology
  • Propranolol / pharmacology
  • Species Specificity
  • Xenopus

Substances

  • Adrenergic beta-Antagonists
  • Potassium Channels, Voltage-Gated
  • Propanolamines
  • ICI 118551
  • Propranolol
  • Metoprolol