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Lung tissue mechanics predict lung hypoplasia in a rabbit model for congenital diaphragmatic hernia

Several animal models have been proposed to study the pathophysiology of congenital diaphragmatic hernia (CDH). Surgical induction of CDH in fetal rabbits during the pseudoglandular phase has been shown to induce severe pulmonary hypoplasia, but functional studies in this model are scarce. We aimed...

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Bibliographic Details
Published in:Pediatric pulmonology 2007-06, Vol.42 (6), p.505-512
Main Authors: Flemmer, Andreas W., Jani, Jacques C., Bergmann, Florian, Muensterer, Oliver J., Gallot, Denis, Hajek, Kerstin, Sugawara, Junichi, Till, Holger, Deprest, Jan A.
Format: Article
Language:English
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Summary:Several animal models have been proposed to study the pathophysiology of congenital diaphragmatic hernia (CDH). Surgical induction of CDH in fetal rabbits during the pseudoglandular phase has been shown to induce severe pulmonary hypoplasia, but functional studies in this model are scarce. We aimed to measure neonatal pulmonary impedance and related it to the severity of lung hypoplasia. CDH was surgically created in rabbits at 23 days of gestation. Following cesarean delivery at term (31 days) pups were subjected to measurement of total lung capacity (TLC), lung to body weight ratio (LBWR) and lung impedance by forced oscillation technique (FOT). Airway resistance (Raw), tissue elastance (HL), tissue damping (GL), and hysteresivity (η) (GL/HL) were calculated from impedance data. Twelve CDH fetuses and 15 controls were available for final analysis. LBWR and TLC were significantly lower in the CDH group compared to gestational and age matched controls (P 
ISSN:8755-6863
1099-0496
DOI:10.1002/ppul.20618