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Honeymoon Period in Newborn Rats With CDH Is Associated With Changes in the VEGF Signaling Pathway

Overview
Journal Front Pediatr
Specialty Pediatrics
Date 2021 Aug 2
PMID 34336744
Citations 1
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Abstract

Patients with congenital diaphragmatic hernia (CDH) have a short postnatal period of ventilatory stability called the honeymoon period, after which changes in pulmonary vascular reactivity result in pulmonary hypertension. However, the mechanisms involved are still unknown. The aim of this study was to evaluate mechanical ventilation's effect in the honeymoon period on VEGF, VEGFR-1/2 and eNOS expression on experimental CDH in rats. Neonates whose mothers were not exposed to nitrofen formed the control groups (C) and neonates with left-sided defects formed the CDH groups (CDH). Both were subdivided into non-ventilated and ventilated for 30, 60, and 90 min ( = 7 each). The left lungs ( = 4) were evaluated by immunohistochemistry of the pulmonary vasculature (media wall thickness), VEGF, VEGFR-1/2 and eNOS. Western blotting ( = 3) was performed to quantify the expression of VEGF, VEGFR-1/2 and eNOS. CDH had lower biometric parameters than C. Regarding the pulmonary vasculature, C showed a reduction in media wall thickness with ventilation, while CDH presented reduction with 30 min and an increase with the progression of the ventilatory time (honeymoon period). CDH and C groups showed different patterns of VEGF, VEGFR-1/2 and eNOS expressions. The receptors and eNOS findings were significant by immunohistochemistry but not by western blotting, while VEGF was significant by western blotting but not by immunohistochemistry. VEGF, its receptors and eNOS were altered in CDH after mechanical ventilation. These results suggest that the VEGF-NO pathway plays an important role in the honeymoon period of experimental CDH.

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References
1.
Barghorn A, Koslowski M, Kromminga R, Hufnagl P, Tennstedt C, Vogel M . Alpha-smooth muscle actin distribution in the pulmonary vasculature comparing hypoplastic and normal fetal lungs. Pediatr Pathol Lab Med. 1998; 18(1):5-22. View

2.
Shinkai M, Shinkai T, Pirker M, Montedonico S, Puri P . Effect of nitric oxide on the development of nitrofen-induced fetal hypoplastic lung explants. J Pediatr Surg. 2005; 40(1):17-21. DOI: 10.1016/j.jpedsurg.2004.09.007. View

3.
Sbragia L, Nassr A, Goncalves F, Schmidt A, Zuliani C, Garcia P . VEGF receptor expression decreases during lung development in congenital diaphragmatic hernia induced by nitrofen. Braz J Med Biol Res. 2014; 47(2):171-8. PMC: 4051183. DOI: 10.1590/1414-431X20133221. View

4.
Papapetropoulos A, Garcia-Cardena G, Madri J, Sessa W . Nitric oxide production contributes to the angiogenic properties of vascular endothelial growth factor in human endothelial cells. J Clin Invest. 1998; 100(12):3131-9. PMC: 508526. DOI: 10.1172/JCI119868. View

5.
Parenti A, Morbidelli L, Cui X, Douglas J, Hood J, Granger H . Nitric oxide is an upstream signal of vascular endothelial growth factor-induced extracellular signal-regulated kinase1/2 activation in postcapillary endothelium. J Biol Chem. 1998; 273(7):4220-6. DOI: 10.1074/jbc.273.7.4220. View