Calcium equally increases the internal calcium recirculation fraction before and after beta-blockade in canine left ventricles

Heart Vessels. 1997;12(6):280-6. doi: 10.1007/BF02766804.

Abstract

We studied whether intracoronary Ca administration after beta-blockade would increase the internal Ca recirculation fraction (RF) analogously to the Ca administration before beta-blockade. This was performed in excised cross-circulated canine hearts. We analyzed the exponential decay component of the postextrasystolic potentiation (PESP) following a spontaneous extrasystole. All the PESPs decayed in alternans with atrial pacing at a constant rate. We obtained the time constant (tau(e)) of the monoexponential decay component of the alternans PESP. An increment of intracoronary Ca by 1.5 mmol/l enhanced the left ventricular contractility index Emax (end-systolic maximum elastance) by 2.5 times before and after beta-blockade with propranolol. The intracoronary Ca after beta-blockade slightly but significantly increased tau(e), and hence increased RF calculated from tau(e) by RF = exp(-1/tau(e)). This was analogous to the slightly increased tau(e) and RF with Ca before beta-blockade. We speculate that the myocardial cyclic AMP-dependent phosphorylation level would not significantly alter the effect of intracoronarily administered Ca on myocardial Ca handling, in terms of tau(e) and RF.

Publication types

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

MeSH terms

  • Adenosine Monophosphate / metabolism
  • Adrenergic beta-Antagonists / pharmacology*
  • Animals
  • Arrhythmias, Cardiac / drug therapy
  • Arrhythmias, Cardiac / metabolism
  • Arrhythmias, Cardiac / physiopathology
  • Calcium / administration & dosage
  • Calcium / pharmacokinetics*
  • Calcium Channels / drug effects
  • Calcium Channels / metabolism*
  • Coronary Vessels
  • Disease Models, Animal
  • Dogs
  • Electrocardiography / drug effects
  • Heart Ventricles / drug effects
  • Heart Ventricles / metabolism*
  • Heart Ventricles / physiopathology
  • Injections, Intra-Arterial
  • Myocardial Contraction / drug effects
  • Propranolol / pharmacology*

Substances

  • Adrenergic beta-Antagonists
  • Calcium Channels
  • Adenosine Monophosphate
  • Propranolol
  • Calcium