Contributions of heart rate and contractility to myocardial oxygen balance during exercise

Am J Physiol Heart Circ Physiol. 2003 Feb;284(2):H676-82. doi: 10.1152/ajpheart.00564.2002. Epub 2002 Oct 24.

Abstract

The respective contributions of heart rate (HR) reduction and left ventricular (LV) negative inotropy to the effects of antianginal drugs are debated. Accordingly, eight instrumented dogs were investigated during exercise at spontaneous and paced HR (250 beats/min) after administration of either saline, atenolol, or ivabradine (selective pacemaker current channel blocker). During exercise, atenolol and ivabradine (both 1 mg/kg iv) similarly reduced HR (-30% from 222 +/- 5 beats/min), and LV mean ejection wall stress was not altered. LV dP/dt(max) was reduced by atenolol but not ivabradine. Diastolic time (DT) was increased by atenolol versus saline (195 +/- 6 vs. 123 +/- 4 ms, respectively) and to a greater extent by ivabradine (233 +/- 11 ms). Myocardial oxygen consumption (MVo(2)) was lower under ivabradine and atenolol versus saline (6.7 +/- 0.6 and 4.7 +/- 0.4 vs. 8.1 +/- 0.6 ml/min, respectively, P < 0.05). Under pacing, DT and MVo(2) were similar between ivabradine and saline but significantly reduced with atenolol. Thus HR reduction and negative inotropy equally contribute to the reduction in MVo(2) during exercise in the normal heart. The negative inotropy limits the increase in DT afforded by HR reduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Arrhythmia Agents / pharmacology
  • Atenolol / pharmacology
  • Benzazepines / pharmacology
  • Cardiac Pacing, Artificial
  • Dogs
  • Heart Rate / physiology*
  • Hemodynamics / physiology
  • Ivabradine
  • Motor Activity / physiology*
  • Myocardial Contraction / physiology*
  • Myocardium / metabolism*
  • Oxygen Consumption / physiology*
  • Stroke Volume / drug effects
  • Ventricular Function, Left / physiology

Substances

  • Anti-Arrhythmia Agents
  • Benzazepines
  • Ivabradine
  • Atenolol