Disparate force-frequency effects of pimobendan and dobutamine in conscious dogs with tachycardia-induced cardiomyopathy

J Card Fail. 2002 Dec;8(6):423-30. doi: 10.1054/jcaf.2002.129658.

Abstract

Background: This study was designed to examine how a calcium sensitizer, pimobendan, affected a force-frequency response (FFR) as compared to the beta-adrenergic agonist dobutamine.

Methods and results: Left ventricular (LV) contractility and relaxation were evaluated by the slope (Ees) of the LV end-systolic pressure-volume relation and the time constant (Tau) of LV pressure decay. Using 6 conscious dogs with tachycardia-induced heart failure, the FFR was examined before and after administration of dobutamine (6 microg/kg/min) or pimobendan (0.5 mg/kg). Despite the similar inotropic and lusitropic action at the baseline heart rate, pimobendan and dobutamine showed different FFR and relaxation-frequency responses. Before administration of these drugs, there was no significant increase in LV contractility and relaxation by increasing heart rate. However, dobutamine amplified FFR (Ees: +3.1 +/- 1.4, P <.05) as compared with Ees for a comparable increase in heart rate before administration of the drug. On the other hand, pimobendan showed relatively mild amplification of FFR compared with dobutamine (Ees: +1.9 +/- 1.1, P <.05). The relaxation-frequency response tended to increase with dobutamine but not with pimobendan.

Conclusions: Mild amplification of FFR observed in pimobendan suggests that this agent could be used more safely than beta-adrenergic agent when heart rate is increased, as seen with exercise.

Publication types

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

MeSH terms

  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Cardiac Pacing, Artificial
  • Cardiotonic Agents / pharmacology*
  • Dobutamine / pharmacology*
  • Dogs
  • Heart Failure / etiology*
  • Heart Failure / physiopathology*
  • Heart Rate / drug effects
  • Myocardial Contraction / drug effects*
  • Pyridazines / pharmacology*
  • Stimulation, Chemical
  • Stroke Volume / drug effects
  • Tachycardia / complications*
  • Tachycardia / physiopathology*
  • Ventricular Pressure / drug effects

Substances

  • Adrenergic beta-Agonists
  • Cardiotonic Agents
  • Pyridazines
  • pimobendan
  • Dobutamine