S. Oparil et al., ENDOTHELIN-A RECEPTOR ANTAGONIST PREVENTS ACUTE HYPOXIA-INDUCED PULMONARY-HYPERTENSION IN THE RAT, American journal of physiology. Lung cellular and molecular physiology, 12(1), 1995, pp. 95-100
Exposure to hypoxia is associated with increased pulmonary artery pres
sure and plasma endothelin-1 (ET-1) levels and with selective enhancem
ent in ET-1 peptide and mRNA and endothelin-A (ET(A)) receptor mRNA le
vels in rat lung. The current study tested the hypothesis that endogen
ous ET-1 can account for hypoxia-induced pulmonary hypertension via a
paracrine effect on ET(A) receptors in lung. Intravenous infusion of t
he ET(A) receptor antagonist BQ-123 (D-Trp-D-Asp-Pro-D-Val-Leu) (0.4 m
g/mu l at 1 mu l/h) into Sprague-Dawley rats beginning 4 h before and
for 90 min during normobaric hypoxia (10% O-2) markedly attenuated the
hypoxic response: mean pulmonary artery pressure increased from 17.2
+/- 0.7 to 29.0 +/- 1.2 mmHg in saline control rats but did not increa
se from baseline in BQ-123-treated rats. BQ-123 did not alter systemic
arterial pressure, heart rate, or plasma endothelin-1 levels. These f
indings suggest that ET-1 synthesized in lung in response to hypoxia a
cts locally on ET(A) receptors to cause pulmonary hypertension.