Thromboxane A(2) receptors mediate pulmonary hypertension in 60% oxygen-exposed newborn rats by a cyclooxygenase-independent mechanism

Am J Respir Crit Care Med. 2002 Jul 15;166(2):208-14. doi: 10.1164/rccm.200112-124OC.

Abstract

Endothelin-1 (ET-1) mediates the development of pulmonary hypertension (PHT) in newborn rats exposed to 60% O(2) for 14 days, a model for human chronic neonatal lung injury. ET-1 production by d-14 rat pulmonary artery smooth muscle cells in vitro was markedly increased by thromboxane (TX) A(2) receptor agonists and inhibited by a competitive antagonist. We hypothesized that stimulation of the TX A(2) receptor contributed to O(2)-mediated PHT in vivo. Newborn rat pups received daily intraperitoneal injections of L670596, a competitive TX A(2) receptor antagonist, or 5,5-dimethyl-3-(3-fluorophenyl)4-(4-methylsulfonyl)phenyl-2(5H)-furanone (DFU), a cyclooxygenase-2 inhibitor, during 14 days of 60% O(2) or air exposure. L670596, but not DFU, prevented 60% O(2)-mediated right ventricular and small pulmonary vessel smooth muscle hypertrophy. Lung ET-1 content was significantly reduced by L670596 in 60% O(2)-exposed animals. We conclude that TX A(2) receptor activation, though not by TX A(2), caused upregulation of ET-1 and PHT in this model. A likely mediator is the stable lipid peroxidation product, 8-iso-prostane, which acts as an incidental ligand of the TX A(2) receptor and is a potent inducer of ET-1 production by cultured d-14 rat pulmonary artery smooth muscle cells in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid / pharmacology
  • Animals
  • Animals, Newborn
  • Blotting, Western
  • Carbazoles / pharmacology
  • Cells, Cultured
  • Cyclooxygenase Inhibitors / pharmacology
  • Dinoprost* / analogs & derivatives*
  • Endothelin-1 / metabolism
  • F2-Isoprostanes / metabolism
  • F2-Isoprostanes / pharmacology
  • Furans / pharmacology
  • Hypertension, Pulmonary / metabolism
  • Hypertension, Pulmonary / physiopathology*
  • Hypertrophy, Right Ventricular / physiopathology
  • Immunohistochemistry
  • Lung / metabolism
  • Muscle, Smooth, Vascular / metabolism
  • Oxygen / physiology
  • Oxygen / toxicity*
  • Prostaglandin Antagonists / pharmacology
  • Prostaglandin-Endoperoxide Synthases / physiology*
  • Pulmonary Artery / metabolism
  • Rats
  • Receptors, Thromboxane / antagonists & inhibitors
  • Receptors, Thromboxane / physiology*
  • Thromboxane B2 / metabolism
  • Up-Regulation
  • Vasoconstrictor Agents / pharmacology

Substances

  • 5,5-dimethyl-3-(3-fluorophenyl)-4-(4-methylsulfonyl)phenyl-2(5H)-furanone
  • Carbazoles
  • Cyclooxygenase Inhibitors
  • Endothelin-1
  • F2-Isoprostanes
  • Furans
  • Prostaglandin Antagonists
  • Receptors, Thromboxane
  • Vasoconstrictor Agents
  • L 670596
  • 8-epi-prostaglandin F2alpha
  • Thromboxane B2
  • 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid
  • Dinoprost
  • Prostaglandin-Endoperoxide Synthases
  • Oxygen