Selective attenuation of isoproterenol-stimulated arrhythmic activity by a partial agonist of adenosine A1 receptor

Circulation. 2002 Jan 1;105(1):118-23. doi: 10.1161/hc0102.101392.

Abstract

Background: The goal of this study was to examine the hypothesis that a partial agonist of the adenosine A1 receptor (A1AdoR) may cause a greater attenuation of catecholamine-induced ventricular arrhythmic activity than of contractility.

Methods and results: The effects of CVT-2759 and adenosine, a partial and a full agonist of the A1AdoR, on isoproterenol-stimulated arrhythmic activity and contractility of guinea pig isolated ventricular myocytes were determined. CVT-2759 (10 micromol/L) and adenosine (10 micromol/L) significantly inhibited isoproterenol-induced arrhythmic activity (aftercontraction and transient inward current) but did not reduce the amplitudes of twitch shortening and L-type Ca2+ current. Increasing the concentration of the full agonist adenosine from 10 to 100 micromol/L, however, caused significant attenuation of twitch shortening as well as aftercontractions, whereas increasing the concentration of the partial agonist CVT-2759 from 10 to 100 micromol/L did not. CVT-2759 also significantly inhibited isoproterenol-induced spontaneous ventricular beats in isolated hearts. In contrast to adenosine, CVT-2759 neither activated adenosine-sensitive K+ current nor shortened the duration of the atrial APD.

Conclusions: The present results support the hypothesis and suggest a potential role for a partial agonist of the A1AdoR in the treatment of cardiac arrhythmias.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine / pharmacology
  • Animals
  • Arrhythmias, Cardiac / chemically induced
  • Arrhythmias, Cardiac / physiopathology
  • Arrhythmias, Cardiac / prevention & control*
  • Calcium Channels, L-Type / drug effects
  • Calcium Channels, L-Type / physiology
  • Cells, Cultured
  • Female
  • Guinea Pigs
  • Heart / drug effects
  • Heart / physiopathology
  • Heart Ventricles / cytology
  • Heart Ventricles / drug effects
  • Heart Ventricles / physiopathology
  • In Vitro Techniques
  • Isoproterenol / administration & dosage
  • Male
  • Membrane Potentials / drug effects
  • Myocardial Contraction / drug effects
  • Purinergic P1 Receptor Agonists*
  • Purines / pharmacology*

Substances

  • Calcium Channels, L-Type
  • Purinergic P1 Receptor Agonists
  • Purines
  • CVT 2759
  • Adenosine
  • Isoproterenol