Loading of calcium and strontium into the sarcoplasmic reticulum in rat ventricular muscle

J Mol Cell Cardiol. 2000 Jul;32(7):1285-300. doi: 10.1006/jmcc.2000.1162.

Abstract

Previous work suggests that strontium ions (Sr(2+)) are less effective than calcium ions (Ca(2+)) at supporting excitation-contraction (EC) coupling in cardiac muscle. We therefore tested whether this was due to differences in the uptake and release of Ca(2+)and Sr(2+)by the sarcoplasmic reticulum (SR) of rat ventricular trabeculae and myocytes at 22-24 degrees C. In permeabilized trabeculae, isometric contractions activated by exposure to Ca(2+)- and Sr(2+)-containing solutions produced similar maximal force, but were four times more sensitive to Ca(2+)than to Sr(2+). The rate of loading and maximal SR capacity for caffeine-releasable Ca(2+)and Sr(2+)were similar. In isolated, voltage-clamped ventricular myocytes, the SR content was measured as Na(+)-Ca(2+)exchange current during caffeine-induced SR cation releases. The SR Ca(2+)load reached a steady maximum during a train of voltage clamp depolarizations. A similar maximal Sr(2+)load was not observed, suggesting that the SR capacity for Sr(2+)exceeds that for Ca(2+). Therefore, the relative inability of Sr(2+)to support cardiac EC coupling appears not to be due to failure of the SR to sequester Sr(2+). Instead, increases in cytosolic [Sr(2+)] seem to poorly activate Sr(2+)release from the SR.

Publication types

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

MeSH terms

  • Animals
  • Caffeine / pharmacology
  • Calcium / metabolism*
  • Calcium / pharmacokinetics
  • Cations
  • Central Nervous System Stimulants / pharmacology
  • Electrophysiology
  • Female
  • Heart Ventricles / drug effects
  • Heart Ventricles / metabolism*
  • In Vitro Techniques
  • Kinetics
  • Male
  • Myocardial Contraction / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Saponins / pharmacology
  • Sarcolemma / metabolism
  • Sarcoplasmic Reticulum / drug effects
  • Sarcoplasmic Reticulum / metabolism*
  • Strontium / metabolism*
  • Strontium / pharmacokinetics
  • Time Factors

Substances

  • Cations
  • Central Nervous System Stimulants
  • Saponins
  • Caffeine
  • Calcium
  • Strontium