Positive force- and [Ca2+]i-frequency relationships in rat ventricular trabeculae at physiological frequencies

Am J Physiol. 1999 Jan;276(1):H9-H18. doi: 10.1152/ajpheart.1999.276.1.H9.

Abstract

The isometric force-frequency relationship of isolated rat ventricular trabeculae (diameter <250 micrometer) was examined at 24, 30, and 37 degreesC at stimulation frequencies (0.1-12 Hz) encompassing the physiological range. Some muscles were microinjected with fura PE3 to monitor the diastolic and systolic intracellular concentration of Ca2+ ([Ca2+]i). At a near-physiological external Ca2+ concentration ([Ca2+]o) of 1 mM, a positive force-frequency relationship was demonstrated at all temperatures. The force-frequency relationship became negative at high frequencies (e. g., >6 Hz at 30 degreesC) at 1 mM [Ca2+]o or at low frequencies at 8 mM [Ca2+]o. The twitch and Ca2+ transient became shorter as stimulation frequency increased; these changes were related to changes in systolic, rather than diastolic, [Ca2+]i and were not blocked by inhibitors of Ca2+/calmodulin-dependent protein kinase II. The positive force-frequency relationship of rat trabeculae was caused by a frequency-dependent loading of the sarcoplasmic reticulum (SR) with Ca2+. We suggest that at high frequencies, or under conditions of Ca2+ overload, this loading saturates. Processes that tend to decrease SR Ca2+ release will then predominate, resulting in a negative force-frequency relationship.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium-Calmodulin-Dependent Protein Kinases / antagonists & inhibitors
  • Electric Stimulation
  • Enzyme Inhibitors / pharmacology
  • Homeostasis / physiology
  • Intracellular Membranes / metabolism*
  • Male
  • Myocardial Contraction / physiology*
  • Osmolar Concentration
  • Rats
  • Rats, Inbred BN
  • Rats, Inbred Lew
  • Rats, Wistar
  • Temperature
  • Time Factors
  • Ventricular Function / physiology*

Substances

  • Enzyme Inhibitors
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Calcium