Direct and indirect actions of dopamine on tracheal smooth muscle.

Abstract

The effects of dopamine (DA) were studied on guinea-pig isolated tracheal chains. At a low concentration (10−6M) DA occasionally produced a small contraction; this was followed by a dose-dependent relaxation 3×10−6–3×10−3 M). On a molar basis, DA was about 40 times less potent than noradrenaline (NA) in relaxing tracheal chains, and about 2700 times less potent than isoprenaline (ISO). The maximum degree of relaxation obtained with each drug was the same. Pretreatment of the guinea-pig with reserpine (5 mg/kg) resulted in a 3-fold shift of the DA curve to the right without concomitantly affecting the ISO doseresponse curve. Reserpine completely abolished the relaxant effects of tyramine, but a small contractile response remained. Desipramine (DMI), at a concentration of 10−5 M, caused a 4-fold shift of the DA curve to th right. The same concentration of DMI resulted in a shift to the left of the NA dose-response curve by about 8-fold. Benztropine (10−5 M) and haloperidol (10−5 M and 3×10−5 M) did not affect the DA dose-response curve. The DA-induced relaxation was inhibited by propranolol (10−8–10−6 M) in a dose-dependent manner. The higher concentrations of propranolol (10−7 and 10−6 M) unmasked the contractile effect of DA. In the presence of propranolol, phentolamine (10−5 M) abolished the contractile effect of DA. It is concluded that DA has both direct and indirect actions on guinea-pig isolated tracheal smooth muscle. The relaxant effects of DA are predominantly due to a direct action on smooth muscle β-adrenoceptors, with a component due to release of NA from adrenergic nerves. The contractile effects, which under normal conditions are masked by the relaxant effect of DA, are mediated by functional α-adrenoceptors. There is no evidence for either specific dopaminergic nerves, uptake mechanisms or receptors in guinea-pig trachealis muscle.