High intracellular Na+ preserves myocardial function at low heart rates in isolated myocardium from failing hearts

Eur J Heart Fail. 2006 Nov;8(7):673-80. doi: 10.1016/j.ejheart.2006.01.013. Epub 2006 Mar 15.

Abstract

We investigated the hypothesis that increased intracellular [Na+]i in heart failure contributes to preservation of SR Ca2+ load which may become particularly evident at slow heart rates. [Na+]i in SBFI-loaded myocytes from rabbits with pacing-induced heart failure (PHF) was significantly higher at each frequency as compared to Sham-operated animals. Furthermore, PHF rabbits demonstrated reduced SR Ca2+-ATPase protein levels (-37%, p < 0.04) but unchanged Na+/Ca2+ exchanger protein levels. At 0.25 Hz, isometric force was similar in cardiac trabeculae from PHF rabbits as compared to control (PHF, 3.6+/-1.3; Sham, 4.4+/-0.6 mN/mm2). Rapid cooling contractures (RCCs) were unchanged indicating preserved SR Ca2+ load at this frequency. In Sham, isometric twitch force increased with rising frequencies to 29.0+/-2.8 mN/mm2 at 3.0 Hz (p < 0.05) as compared to 0.25 Hz. RCCs showed a parallel increase by 186+/-47% (p < 0.01). In PHF, frequency-dependent increase in force (15.8+/-4.7 mN/mm2 at 3.0 Hz) and RCCs (increase by 70+/-40%) were significantly blunted. Thus, in PHF in rabbits SR Ca2+ load is preserved at low frequencies despite decreased SR Ca2+-ATPase expression. This may result from [Na+]i-dependent changes in Na+/Ca2+ exchanger activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium-Transporting ATPases / metabolism*
  • Disease Models, Animal
  • Electric Stimulation
  • Heart Failure / metabolism*
  • Muscle Cells
  • Rabbits
  • Sarcoplasmic Reticulum / metabolism
  • Sodium / metabolism*
  • Sodium-Calcium Exchanger*

Substances

  • Sodium-Calcium Exchanger
  • Sodium
  • Calcium-Transporting ATPases