Proarrhythmic effects of pinacidil are partially mediated through enhancement of catecholamine release in isolated perfused guinea-pig hearts

J Mol Cell Cardiol. 1998 Feb;30(2):415-23. doi: 10.1006/jmcc.1997.0605.

Abstract

The contribution of adrenergic stimulation to the proarrhythmic effects of pinacidil (30 microM), an opener of ATP-sensitive potassium channels (K+ATP), was tested in an isolated guinea-pig heart model of global ischemia (10 min) and reperfusion (10 min). None (0%) of the control hearts (n=10) elicited arrhythmias during ischemia or reperfusion. In the pinacidil-treated group, one heart (5%) experienced episodes of ventricular tachycardia (VT)/fibrillation (VF) during normoxia. During ischemia, 63% (12 out of 19) of pinacidil-treated hearts exhibited episodes of VT or VF. Hearts not in VT or VF (n=7) at the time of reperfusion, exhibited 71% VT and 43% VT/VF upon reperfusion. Proarrhythmic effects of pinacidil during ischemia or reperfusion were completely reversed by glyburide (n=9; 10 microM), a K+ATP antagonist, or nadolol (n=9; 3 microM), a beta-adrenergic antagonist. Isoproterenol (n=10; 50 nM), a beta-adrenergic agonist, induced a 20% incidence of ischemic VT and VF, and a 70% incidence of reperfusion VF, while methoxamine (n=10; 10 microM), an alpha-adrenergic agonist, demonstrated little proarrhythmia (20% VT/VF at reperfusion only). Proarrhythmic effects of isoproterenol were reversed by nadolol, but not glyburide. Pinacidil caused a slight potentiation of tachycardia induced by a bolus injection of tyramine (30 micro g), an indirectly acting sympathomimetic, but bolus injections of pinacidil (100 micro g) had no effect on heart rate. Nisoxetine, a catecholamine uptake 1 inhibitor, had no proarrhythmic effects when given alone. Catecholamine levels were reduced in pinacidil-treated hearts relative to vehicle-treated. In conclusion, it is suggested that the proarrhythmic effects of pinacidil following global ischemia and reperfusion in the isolated perfused guinea-pig heart appears to involve stimulation of beta-adrenoceptors. These proarrhythmic effects of pinacidil do not appear to be mediated solely through direct opening of K+ATP, but rather through an indirect enhancement of catecholamine release.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adrenergic Agonists / pharmacology
  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Arrhythmias, Cardiac / etiology*
  • Arrhythmias, Cardiac / metabolism
  • Arrhythmias, Cardiac / physiopathology*
  • Epinephrine / metabolism*
  • Fluoxetine / analogs & derivatives
  • Fluoxetine / pharmacology
  • Glyburide / pharmacology
  • Guanidines / toxicity*
  • Guinea Pigs
  • Heart / drug effects*
  • Heart / physiology*
  • In Vitro Techniques
  • Isoproterenol / pharmacology
  • Methoxamine / pharmacology
  • Myocardial Reperfusion Injury / complications
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / physiopathology
  • Myocardium / metabolism
  • Nadolol / pharmacology
  • Norepinephrine / metabolism*
  • Perfusion
  • Pinacidil
  • Potassium Channels / drug effects*
  • Potassium Channels / metabolism
  • Tyramine / pharmacology

Substances

  • Adrenergic Agonists
  • Adrenergic beta-Antagonists
  • Guanidines
  • Potassium Channels
  • Fluoxetine
  • nisoxetine
  • Nadolol
  • Pinacidil
  • Adenosine Triphosphate
  • Methoxamine
  • Isoproterenol
  • Glyburide
  • Norepinephrine
  • Tyramine
  • Epinephrine