Effects of oximes, diacetylmonoxime, pyridine-2-aldoxime, and pyridine-2-aldoxime methochloride, on the electrical and mechanical activities of guinea pig cardiac ventricular muscles

J Pharmacobiodyn. 1985 Jun;8(6):425-31. doi: 10.1248/bpb1978.8.425.

Abstract

Effects of 3 oximes, diacetylmonoxime (DAM), pyridine-2-aldoxime (PAM) and pyridine-2-aldoxime methochloride (2-PAM), on the normal electrical and mechanical activities and on the slow response action potentials were examined in the guinea pig ventricular muscles. DAM and long-term exposure to high concentrations of PAM produced decreases in contractile force, action potential duration and slow response action potentials, whereas 2-PAM and low concentrations of PAM tended to increase these parameters. Thus, these 3 oximes did not act uniformly on cardiac muscle. It was speculated that DAM and high concentrations of PAM may act as slow channel inhibitors, whereas 2-PAM and low concentrations of PAM may act as slow channel activators.

MeSH terms

  • Action Potentials / drug effects
  • Animals
  • Butanones / pharmacology*
  • Diacetyl / analogs & derivatives
  • Diacetyl / pharmacology*
  • Diltiazem / pharmacology
  • Guinea Pigs
  • Heart / physiology*
  • In Vitro Techniques
  • Male
  • Myocardial Contraction / drug effects*
  • Pralidoxime Compounds / pharmacology*
  • Time Factors
  • Verapamil / pharmacology

Substances

  • Butanones
  • Pralidoxime Compounds
  • diacetylmonoxime
  • Verapamil
  • Diltiazem
  • Diacetyl
  • pralidoxime