4.1 Article

VEGF levels in humans and animal models with RDS and BPD: Temporal relationships

Journal

EXPERIMENTAL LUNG RESEARCH
Volume 38, Issue 4, Pages 192-203

Publisher

TAYLOR & FRANCIS INC
DOI: 10.3109/01902148.2012.663454

Keywords

VEGF; bronchopulmonary dysplasia; neonatal lung disease; respiratory distress syndrome

Funding

  1. American Heart Association [0755843T]
  2. American Thoracic Society [ATS-07-005]
  3. NHLBI of the National Institutes of Health, USA [HL-74195, HL-085103]

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Respiratory distress syndrome (RDS) and bronchopulmonary dysplasia (BPD) contribute significantly to neonatal morbidity and mortality. Pulmonary function depends on the interaction between alveolar microvasculature and airspace development. While it has been shown in various animal models that vascular endothelial growth factor (VEGF) and its receptors increase in normal animal lung development, its pathophysiological role in neonatal respiratory failure is not yet entirely clear. Current animal and human studies exhibit controversial results. Though animal models are invaluable tools in the study of human lung disease, inherent differences in physiology mandate clarification of the timing of these studies to ensure that they appropriately correlate with the human stages of lung development. The purpose of this review article is to highlight the importance of considering the temporal relationship of VEGF and lung development in human neonates and developmentally-appropriate animal models with RDS and BPD.

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