Selective or nonselective endothelin antagonists in porcine hypoxic pulmonary hypertension

We evaluated the hemodynamic effects of various endothelin (ET) receptor antagonists using selective and nonselective ET A and ET B receptor blockade in hypoxic pigs in vivo. BMS-182874 (10 mg/kg i.v.) TBC-11251z (10 mg/kg i.v.), selective ET A receptor antagonists, attenuated hypoxia (FiO 2 0.1)-evoked increase in pulmonary arterial pressure and pulmonary vascular resistance. Bosentan (10 mg/kg i.v.) a non-selective ET A and ET B receptor antagonist, cause essentially similar effects as ET A antagonism alone. No effects were observed after selective ET B blockade using BQ-788 (total dose 1 mg i.v.). The vasoconstrictor effect of exogenous ET was most effectively antagonized by TBC-11251z, followed by BMS-182874 and bosentan. The pulmonary vasodilator effect exerted by exogenous ET during hypoxia was reversed by BQ-788 and bosentan but not by TBC-11251z or BMS-182874. We can therefore conclude that ET contributes to hypoxic pulmonary vasoconstriction primarily through ET A receptor activation.