Denopamine (beta 1-selective adrenergic receptor agonist) and isoproterenol (non-selective beta-adrenergic receptor agonist) equally increase heart rate and myocardial oxygen consumption in dog heart

Jpn Circ J. 1991 Oct;55(10):972-82. doi: 10.1253/jcj.55.972.

Abstract

The effects of denopamine (a beta 1-selective adrenergic receptor agonist) and isoproterenol (a non-selective beta-adrenergic receptor agonist) on heart rate, left ventricular contractility, and left ventricular oxygen consumption (VO2) at the same left ventricular volume were compared in excised cross-circulated dog hearts. Denopamine and isoproterenol increased heart rate and VO2 to a comparable extent at a comparably increased contractility. Moreover, the oxygen cost of contractility which quantifies VO2 for excitation-contraction coupling was the same between the two agents. These findings contradict the previously reported smaller increases in heart rate and VO2 by denopamine than by isoproterenol in open-chest dog hearts, which have been mainly attributed to the beta 1-selectivity of denopamine. Our results suggest that in isolated and denervated hearts, the degree of beta 1-selectivity of a beta-agonistic agent does not directly determine the relative potencies of its inotropic and chronotropic effects and the oxygen cost of contractility.

Publication types

  • Comparative Study

MeSH terms

  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Dogs
  • Ethanolamines / pharmacology*
  • Heart / drug effects*
  • Heart Rate / drug effects*
  • Isoproterenol / pharmacology*
  • Myocardial Contraction / drug effects
  • Myocardium / metabolism*
  • Oxygen Consumption / drug effects*
  • Regression Analysis
  • Stimulation, Chemical
  • Ventricular Function, Left / drug effects

Substances

  • Adrenergic beta-Agonists
  • Ethanolamines
  • Isoproterenol
  • denopamine