Antenatal fetal VEGF therapy to promote pulmonary maturation in a preterm rabbit model
- PMID: 20181445
- DOI: 10.1016/j.earlhumdev.2010.01.025
Antenatal fetal VEGF therapy to promote pulmonary maturation in a preterm rabbit model
Abstract
Aim: To assess the effects of fetal tracheal administration of VEGF on pulmonary maturation in a preterm rabbit model.
Methods: On day 26 (term=31days), fetal rabbits received recombinant rat VEGF (30microg in 70microL normal saline) or placebo (normal saline 70microL) intratracheally, with or without subsequent tracheal occlusion. Non-operated littermates served as internal controls. Fetuses were harvested on day 28 for morphometric study of the lungs or for mechanical ventilation and measurement of lung mechanics. In total, 96 fetuses from 42 does were used, 47 for ventilation and 49 for morphometry.
Results: In fetuses receiving intratracheal VEGF, an increase in immunoreactivity for Flk-1 was observed throughout the lung parenchyma. Tracheal occlusion (TO) adversely affected pulmonary mechanics as compared to un-occluded controls. That effect is partly reversed by intratracheal VEGF. Intratracheal injection of VEGF without tracheal occlusion improves lung mechanics but no more than what was observed in placebo injected controls.
Conclusion: Antenatal intratracheal VEGF administration was associated with an increase in Flk-1 immunoreactivity. It also improves lung mechanics, however more so when the trachea is occluded. Without TO, the effects were comparable to placebo controls.
Similar articles
-
Effect of maternal administration of betamethasone on peripheral arterial development in fetal rabbit lungs.Neonatology. 2008;93(1):64-72. doi: 10.1159/000107231. Epub 2007 Aug 16. Neonatology. 2008. PMID: 17703103
-
Postnatal lung mechanics, lung composition, and surfactant synthesis after tracheal occlusion vs prenatal intrapulmonary instillation of perfluorocarbon in fetal rabbits.J Pediatr Surg. 2005 Jan;40(1):26-31. doi: 10.1016/j.jpedsurg.2004.09.008. J Pediatr Surg. 2005. PMID: 15868554
-
High-dose vascular endothelial growth factor increases surfactant protein gene expressions in preterm rat lung.Early Hum Dev. 2007 Sep;83(9):581-4. doi: 10.1016/j.earlhumdev.2006.12.005. Epub 2007 Jan 30. Early Hum Dev. 2007. PMID: 17267143
-
[Intrauterine stimulation for fetal respiratory system maturation; benefits and risks].Wiad Lek. 2000;53(9-10):538-45. Wiad Lek. 2000. PMID: 11148922 Review. Polish.
-
The effects of mechanical forces on lung functions.Respir Physiol. 2000 Jan;119(1):1-17. doi: 10.1016/s0034-5687(99)00092-4. Respir Physiol. 2000. PMID: 10701703 Review.
Cited by
-
Antenatal BAY 41-2272 reduces pulmonary hypertension in the rabbit model of congenital diaphragmatic hernia.Am J Physiol Lung Cell Mol Physiol. 2016 Apr 1;310(7):L658-69. doi: 10.1152/ajplung.00178.2015. Epub 2016 Feb 12. Am J Physiol Lung Cell Mol Physiol. 2016. PMID: 26873974 Free PMC article.
-
Ventilation with hyperoxia promotes cochlear bleeding in rabbits with congenital diaphragmatic hernia.Clinics (Sao Paulo). 2024 Nov 5;79:100525. doi: 10.1016/j.clinsp.2024.100525. eCollection 2024. Clinics (Sao Paulo). 2024. PMID: 39504616 Free PMC article.
-
Transcriptome Analysis of the Preterm Rabbit Lung after Seven Days of Hyperoxic Exposure.PLoS One. 2015 Aug 28;10(8):e0136569. doi: 10.1371/journal.pone.0136569. eCollection 2015. PLoS One. 2015. PMID: 26317699 Free PMC article.
-
Structural and molecular regulation of lung maturation by intratracheal vascular endothelial growth factor administration in the normally grown and placentally restricted fetus.J Physiol. 2016 Mar 1;594(5):1399-420. doi: 10.1113/JP271113. Epub 2015 Dec 23. J Physiol. 2016. PMID: 26537782 Free PMC article.
-
Excessive Reversal of Epidermal Growth Factor Receptor and Ephrin Signaling Following Tracheal Occlusion in Rabbit Model of Congenital Diaphragmatic Hernia.Mol Med. 2016 Sep;22:398-411. doi: 10.2119/molmed.2016.00121. Epub 2016 Jul 19. Mol Med. 2016. PMID: 27452320 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical