An analysis of the mechanism of the inotropic action of some milrinone analogues in guinea-pig isolated atria

Br J Pharmacol. 1991 Dec;104(4):867-72. doi: 10.1111/j.1476-5381.1991.tb12519.x.

Abstract

1. It has been reported previously that the milrinone analogues, ethyl 5-cyano-1,6-dihydro-2-methyl-6-oxo-3 pyridine carboxylate (I) and ethyl 5-cyano-1,6-dihydro-2-ethyl-6-oxo-3 pyridine carboxylate (II) exert a positive inotropic effect (EC50 = 15.6 +/- 0.2 microM and 40.3 +/- 0.1 microM) both on spontaneously beating and on electrically driven atria from reserpine-treated guinea-pigs. In the present study the mechanism of the inotropic action of these two agents was investigated. 2. In electrically driven left atrium from reserpine-treated guinea-pigs the EC50 values for inotropic activity for compounds (I) and (II) corresponded to that of milrinone (EC50 = 25 +/- 0.1 microM) but compound (I) induced a greater maximum effect. This corresponded to a percentage increase in developed tension over control of 63 +/- 0.3 whereas the maximum inotropic effect of milrinone was 48 +/- 0.3 and that of compound (II) was 47 +/- 0.2. 3. The inotropic activity of compounds (I) and (II) (10-100 microM) was resistant to propranolol (0.1 microM), thus excluding the involvement of beta-adrenoceptors. 4. Since the inotropism induced by compounds (I) and (II) was not reduced by carbachol (1 nM-0.5 microM), an action involving changes in adenosine 3':5'-cyclic monophosphate (cyclic AMP) can be excluded. 5. The inotropic action of compounds (I) and (II) was blocked selectively by 8-phenyltheophyline (10 microM) or adenosine deaminase (2 u ml-1). 6. Both (I) and (II) inhibited, in an apparently competitive manner, the negative inotropic effect induced by N6-(L-phenylisopropyl) adenosine (L-PIA), a stable adenosine agonist. The pA2 values for (I) and (II) were 4.79 and 4.36, respectively.7. In rat brain compounds (I) and (II) inhibited the specific binding of N6-cyclohexyl[3H]-adenosine- ([3H]-CHA) with an IC50 of 0.18 + 0.01 mM and 0.25 + 0.02 mm, respectively, which were similar to their IC50 values for blocking the PIA-induced negative inotropic effect and which are also in the range of concentrations that are effective in inducing positive inotropism in guinea-pig atria.8. The results from the present study suggest that antagonism of endogenous purines causes positive inotropism without affecting intracellular cyclic AMP levels.

MeSH terms

  • Adenosine / analogs & derivatives
  • Adenosine / pharmacology
  • Adenosine Deaminase Inhibitors
  • Animals
  • Carbachol / pharmacology
  • Cardiotonic Agents / pharmacology*
  • Electric Stimulation
  • Guinea Pigs
  • Heart Atria / drug effects
  • In Vitro Techniques
  • Male
  • Milrinone
  • Myocardial Contraction / drug effects*
  • Phenylisopropyladenosine / pharmacology
  • Propranolol / pharmacology
  • Pyridones / pharmacology*
  • Reserpine / pharmacology
  • Theophylline / analogs & derivatives
  • Theophylline / pharmacology

Substances

  • Adenosine Deaminase Inhibitors
  • Cardiotonic Agents
  • Pyridones
  • ethyl 5-cyano-2-ethyl-1,6-dihydro-6-oxo-3-pyridinecarboxylate
  • Phenylisopropyladenosine
  • N(6)-cyclohexyladenosine
  • ethyl 5-cyano-1,6-dihydro-2-methyl-6-oxo-3-pyridinecarboxylate
  • Reserpine
  • Carbachol
  • Propranolol
  • Theophylline
  • 8-phenyltheophylline
  • Milrinone
  • Adenosine