Effects of α‐adrenoceptor stimulation with phenylephrine in the presence of propranolol on force of contraction, slow inward current and cyclic AMP content in the bovine heart

Abstract

The mechanism of the cyclic AMP‐independent positive inotropic effect of cardiac α‐adrenoceptor stimulation was studied by analyzing the effects of phenylephrine on force of contraction, calcium‐dependent slow action potentials and the slow inward current (Isi) in bovine ventricular trabeculae. The preparations were electrically driven at 0.3 Hz in the presence of propranolol 1 μmol l−1. Phenylephrine increased the force of contraction in a concentration‐dependent manner (maximum about 200% of control at 30 μmol l−1). The effect was surmountably antagonized by phentolamine. The positive inotropic effect of phenylephrine was accompanied by a concentration‐dependent increase in time to peak force and occurred without any detectable increase in cyclic adenosine 3′,5′‐monophosphate (cyclic AMP) levels. The positive inotropic effect of phenylephrine was accompanied by an increase in action potential duration both at 20% and 90% repolarization. Calcium‐dependent slow action potentials were also prolonged by phenylephrine and there was a distinct increase in the maximal rate of depolarization (dV/dtmax) of these slow potentials. These effects were also completely reversible on washing and surmountably blocked by phentolamine. However, the increase in dV/dtmax was smaller than that of isoprenaline in concentrations producing similar inotropic effects. Voltage‐clamp experiments with the single sucrose‐gap method showed that the phenylephrine‐induced increase in force of contraction was associated not only with an increase in peak slow calcium inward current, Isi max, but also with a delay in the inactivation of Isi. Outward currents were not detectably altered by phenylephrine. It is concluded that the α‐adrenoceptor mediated, cyclic AMP‐independent positive inotropic effects of phenylephrine in bovine cardiac muscle are associated with an increase in slow inward current. Additionally, the amount of calcium influx during excitation is probably increased by a delay in the inactivation of Isi. Both effects can explain the phenylephrine‐produced prolongation of the action potential, and probably contribute to the positive inotropic effect of α‐adrenoceptor stimulation. However, as the effect on dV/dtmax is smaller than that of isoprenaline, other (still unknown) mechanisms may also be involved. 1984 British Pharmacological Society