Cardiac electrophysiological effects of levosimendan, a new calcium sensitizer

Gen Pharmacol. 1996 Apr;27(3):551-6. doi: 10.1016/0306-3623(95)02060-8.

Abstract

1. The conventional microelectrode and the patch-clamp techniques were used to study the electrophysiological effects of levosimendan, a new calcium-sensitizing cardiotonic drug, in cardiac ventricular muscle. 2. Levosimendan (5 microM) did not change the main repolarizing currents, such as the inward rectifier potassium, transient outward and the delayed rectifier outward potassium current, in rabbit ventricular myocytes. 3. In rabbit ventricular muscle, levosimendan, at relatively low concentrations (0.1-1 microM), did not change significantly the amplitude of the inward calcium current but increased the amplitude of the twitch tension. 4. In guinea pig ventricular muscle, levosimendan, at higher concentrations (1-5 microM), significantly increased the amplitude of the inward calcium current and the slow-response action potential parameters. 5. It is concluded that levosimendan, in addition to its calcium sensitizing properties characterized by "silent electrophysiology," exhibits cardiac electrophysiological effects similar to those of phosphodies-terase inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Animals
  • Calcium / physiology*
  • Calcium Channels / drug effects
  • Calcium Channels / metabolism
  • Cardiotonic Agents / pharmacology*
  • Electrophysiology
  • Female
  • Guinea Pigs
  • Heart / drug effects
  • Heart / physiology*
  • Hydrazones / pharmacology*
  • In Vitro Techniques
  • Male
  • Membrane Potentials / drug effects
  • Microelectrodes
  • Myocardial Contraction / drug effects
  • Myocardial Contraction / physiology
  • Myocardium / cytology
  • Papillary Muscles / drug effects
  • Patch-Clamp Techniques
  • Pyridazines / pharmacology*
  • Rabbits
  • Simendan

Substances

  • Calcium Channels
  • Cardiotonic Agents
  • Hydrazones
  • Pyridazines
  • Simendan
  • Calcium