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Pediatr Pulmonol. 2012 Nov;47(11):1088-96. doi: 10.1002/ppul.22512. Epub 2012 Feb 10.

Signaling molecules in the fetal rabbit model for congenital diaphragmatic hernia.

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  • 1Laboratory of Physiology and Physiopathology, Faculty of Medicine, Universit√© Libre de Bruxelles, Brussels, Belgium. avuckovi@ulb.ac.be

Abstract

RATIONALE AND OBJECTIVES:

Little is known about molecular changes in lungs of fetal rabbits with surgically induced diaphragmatic hernia (DH). Therefore, we examined in this model gene expressions of pivotal molecules for the developing lung.

METHODS:

At day 23 of gestation, DH was created in 12 fetuses from 4 does. Both lungs from six live DH fetuses and from six unoperated controls were harvested and weighed at term. Transcription of 15 genes involved in alveolarization, angiogenesis, regulation of vascular tone, or epithelial maturation was investigated by real-time quantitative polymerase chain reaction.

MAIN RESULTS:

DH decreased lung-to-body weight ratio (P < 0.001). A bilateral downregulation was seen for genes encoding for tropoelastin (P < 0.01), lysyl oxidase (P < 0.05), fibulin 5 (P < 0.05), and cGMP specific phosphodiesterase 5 (P < 0.05). Lower mRNA levels for endothelial nitric oxide synthase occurred in the ipsilateral lung (P < 0.05).

CONCLUSIONS:

Experimental DH in fetal rabbits disrupted transcription of genes implicated in lung growth and function. Similarities with the human disease make this model appropriate for investigation of new prenatal therapies.

Copyright © 2012 Wiley Periodicals, Inc.

[PubMed - indexed for MEDLINE]
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