Nitric oxide synthases in infants and children with pulmonary hypertension and congenital heart disease.

Respir Res

Neonatology and Pediatric Intensive Care Medicine, Department of General Pediatrics, Heinrich-Heine-University, Duesseldorf, Germany.

Published: November 2009

AI Article Synopsis

  • Nitric oxide is crucial in controlling blood flow in the lungs, especially in cases of pulmonary hypertension associated with congenital heart disease.
  • The study compared nitric oxide synthase expressions (eNOS, iNOS, nNOS) in lung biopsies from infants with and without pulmonary hypertension.
  • Findings showed increased eNOS and iNOS levels in the pulmonary vascular endothelial cells of affected infants, suggesting these changes may help alleviate rising pulmonary artery pressure early on.

Article Abstract

Rationale: Nitric oxide is an important regulator of vascular tone in the pulmonary circulation. Surgical correction of congenital heart disease limits pulmonary hypertension to a brief period.

Objectives: The study has measured expression of endothelial (eNOS), inducible (iNOS), and neuronal nitric oxide synthase (nNOS) in the lungs from biopsies of infants with pulmonary hypertension secondary to cardiac abnormalities (n = 26), compared to a control group who did not have pulmonary or cardiac disease (n = 8).

Methods: eNOS, iNOS and nNOS were identified by immunohistochemistry and quantified in specific cell types.

Measurements And Main Results: Significant increases of eNOS and iNOS staining were found in pulmonary vascular endothelial cells of patients with congenital heart disease compared to control infants. These changes were confined to endothelial cells and not present in other cell types. Patients who strongly expressed eNOS also had strong expression of iNOS.

Conclusion: Upregulation of eNOS and iNOS occurs at an early stage of pulmonary hypertension, and may be a compensatory mechanism limiting the rise in pulmonary artery pressure.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780406PMC
http://dx.doi.org/10.1186/1465-9921-10-110DOI Listing

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