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Endothelin-1 decreases endothelial NOS expression and activity through ET_A receptor-mediated generation of hydrogen peroxide

¹Department of Pediatrics, Northwestern University, Chicago, Illinois; and ²Department of Biomedical and Pharmaceutical Sciences and ³International Heart Institute, University of Montana, Missoula, Montana

Submitted 23 July 2004 ; accepted in final form 4 November 2004

Similar to infants born with persistent pulmonary hypertension of the newborn (PPHN), there is an increase in circulating endothelin-1 (ET-1) and decreased endothelial nitric oxide synthase (eNOS) gene expression in an ovine model of PPHN. These abnormalities lead to vasoconstriction and vascular remodeling. Our previous studies have demonstrated that reactive oxygen species (ROS) levels are elevated in the pulmonary arteries from PPHN lambs and that ET-1 increases ROS production in pulmonary arterial smooth muscle cells (PASMC) in culture. Thus the objective of this study was to determine whether there was a feedback mechanism between the ET-1-mediated increase in ROS in fetal PASMC (FPASMC) and a decrease in eNOS gene expression in fetal pulmonary arterial endothelial cells (FPAEC). Our results indicate that ET-1 increased H₂O₂ levels in FPASMC in an endothelin A receptor-dependent fashion. This was observed in both FPASMC monoculture and in cocultures of FPASMC and FPAEC. Conversely, ET-1 decreased H₂O₂ levels in FPAEC monoculture in an endothelin B receptor-dependent fashion. Furthermore, ET-1 decreased eNOS promoter activity by 40% in FPAEC in coculture with FPASMC. Promoter activity was restored in the presence of catalase. In FPAEC in monoculture treated with 0–100 µM H₂O₂, 12 µM had no effect on eNOS promoter activity, but it increased eNOS protein levels by 50%. However, at 100 µM, H₂O₂ decreased eNOS promoter activity and protein levels in FPAEC by 79 and 40%, respectively. These data suggest a role for smooth muscle cell-derived H₂O₂ in ET-1-mediated downregulation of eNOS expression in children born with PPHN.

pulmonary hypertension; reactive oxygen species; gene expression; cell signaling; nitric oxide synthase; endothelial nitric oxide synthase; endothelin A

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