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Am J Physiol Lung Cell Mol Physiol 284: L316-L323, 2003. First published September 27, 2002; doi:10.1152/ajplung.00228.2002
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Vol. 284, Issue 2, L316-L323, February 2003

Arachidonic acid metabolites and an early stage of pulmonary hypertension in chronically hypoxic newborn pigs

Candice D. Fike, Mark R. Kaplowitz, and Sandra L. Pfister

Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226; and Department of Pediatrics, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157

Our purpose was to determine whether production of arachidonic acid metabolites, particularly cyclooxygenase (COX) metabolites, is altered in 100-400-µm-diameter pulmonary arteries of piglets at an early stage of pulmonary hypertension. Piglets were raised in either room air (control) or hypoxia for 3 days. A cannulated artery technique was used to measure responses of 100-400-µm-diameter pulmonary arteries to arachidonic acid, a prostacyclin analog, or the thromboxane mimetic U46619. Radioimmunoassay was used to determine pulmonary artery production of thromboxane B2 (TxB2) and 6-keto-prostaglandin F1alpha (6-keto-PGF1alpha ), the stable metabolites of thromboxane and prostacyclin, respectively. Assessment of abundances of COX pathway enzymes in pulmonary arteries was determined by immunoblot technique. Arachidonic acid induced less dilation in pulmonary arteries from hypoxic than in pulmonary arteries from control piglets. Pulmonary artery responses to prostacyclin and U46619 were similar for both groups. 6-Keto-PGF1alpha production was reduced, whereas TxB2 production was increased in pulmonary arteries from hypoxic piglets. Abundances of both COX-1 and prostacyclin synthase were reduced, whereas abundances of both COX-2 and thromboxane synthase were unaltered in pulmonary arteries from hypoxic piglets. At least partly due to altered abundances of COX pathway enzymes, a shift in production of arachidonic acid metabolites, away from dilators toward constrictors, may contribute to the early phase of chronic hypoxia-induced pulmonary hypertension in newborn piglets.

cyclooxygenase-1; cyclooxygenase-2; prostacyclin; thromboxane


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