Cardiovascular effects of BRX-005 comparison to bimoclomol

Life Sci. 2000 Aug 25;67(14):1783-9. doi: 10.1016/s0024-3205(00)00755-4.

Abstract

Concentration-dependent effects of BRX-005, the novel heat shock protein coinducer, cardioprotective and vasoprotective agent, on intracellular calcium transients and contractility were studied in Langendorff-perfused guinea pig hearts loaded with the fluorescent calcium indicator dye Fura-2. BRX-005 increased peak left ventricular pressure, the rate of force development and relaxation significantly in a concentration-dependent manner. The amplitude of [Ca2+]i transients was left unaltered by the drug. In contrast to BRX-005, bimoclomol increased both contractility and the amplitude of [Ca2+]i transients. In canine ventricular cardiomyocytes high concentrations of BRX-005 had no effect on depolarization, whereas bimoclomol suppressed action potential upstroke markedly. In guinea pig pulmonary artery preparations precontracted with phenylephrine, BRX-005 induced concentration-dependent relaxation. This effect of BRX-005 was independent of the integrity of endothelium indicating that vasorelaxant effect of the drug develops directly on vascular smooth muscle.

Publication types

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

MeSH terms

  • Action Potentials / drug effects
  • Animals
  • Calcium / metabolism
  • Cardiotonic Agents / pharmacology*
  • Dogs
  • Dose-Response Relationship, Drug
  • Guinea Pigs
  • Heart / drug effects*
  • Heart / physiology
  • Heart Ventricles / cytology
  • Heart Ventricles / drug effects
  • Imides / pharmacology*
  • In Vitro Techniques
  • Muscle, Smooth, Vascular / drug effects
  • Myocardial Contraction / drug effects
  • Myocardium / metabolism
  • Pulmonary Artery / drug effects
  • Pyridines / pharmacology*
  • Ventricular Function, Left / drug effects
  • Ventricular Pressure / drug effects

Substances

  • BRX 005
  • Cardiotonic Agents
  • Imides
  • Pyridines
  • bimoclomol
  • Calcium