Preliminary Experimental Study of Establishing a Lung Development Model with Specific Pathogen Free Preterm Pigs
Abstract
To determine the best time for conducting cesarean section for the establishment of an animal model of lung development with specific pathogen free (SPF) preterm Bama minipigs under the condition of not making medical interventions such as hyperoxia, mechanical ventilation, or medication. Methods SPF Bama sows at gestational day (GD) 113, GD107, GD104, GD101, and GD98 were selected and cesarean sections were performed. Then, the viability of the preterm piglets were observed. Based on their general data, viability, and paraffin sections stained with hematoxylin and eosin, the best time for performing cesarean section in order to build a SPF preterm pig model of lung development was determined. Results Cesarean sections were performed on a total of 7 sows and 55 piglets were delivered, among which 25 were still alive 3 hours after delivery. Seven piglets of GD104 and all piglets of GD107 and GD113 survived, while piglets of GD98 and GD101 all died. The survival rate of piglets of GD104 was 33.33% (7/21). Piglets of GD98 already possessed fully developed physical appearance and lung shape. Piglets from GD104 had better lung expansion and higher density of thin-walled alveoli. The lungs of GD107 piglets were basically fully expanded, and the density of thin-walled alveoli was almost the same as that of normal full-term piglets. Conclusions Findings of this study suggest that SPF preterm piglets of GD104 with no specific pathogen exposure and no medical intervention can be used to establish a SPF preterm pig model of lung development.
Keywords: Preterm, Animal model, Lung, Development
Full Text:
PDFReferences
VOYNOW J A. “New” bronchopulmonary dysplasia and chronic lung disease. Paediatr Respir Rev,2017,24(1): 17–18.
NARDIELLO C, MIŽÍKOVÁ I, MORTY R E, et al. Looking ahead: Where to next for animal models of bronchopulmonary dysplasia? Cell Tissue Res,2017,367(3): 457–468.
CAMINITA F, MERWE M, HANCE F, et al. A preterm pig model of lung immaturity and spontaneous infant respiratory distress syndrome. Am J Physiol Lung Cell Mol Physiol,2015,308(2): 118–129.
BUDDINGTON R K, SANGILD P T, HANCE B, et al. Prenatal gastrointestinal development in the pig and responses after preterm birth. J Anim Sci,2012,90(Suppl 4): 290–298.
ODLE J, LIN X, JACOBI S K, et al. The suckling piglet as an agrimedical model for the study of pediatric nutrition and metabolism. Annu Rev Anim Biosci,2014,2(1): 419–444.
SANGILD P T, THYMANN T, SCHMIDT M, et al. Invited review: The preterm pig as a model in pediatric gastroenterology. J Anim Sci,2013, 91(10): 4713–4729.
MCPHERSON R L, JI F, WU G, et al. Growth and compositional changes of fetal tissues in pigs. J Anim Sci,2004,82(9): 2534–2540. SZPINDA M, SIEDLACZEK W, SZPINDA A, et al. Volumetric growth of the lungs in human fetuses: an anatomical, hydrostatic and statistical study. Surg Radio Anat,2014,36(8): 813–820.
PAEPE M E D, FRIEDMAN R M, GUNDOGAN F, et al. Postmortem lung weight/body weight standards for term and preterm infants. Pediatr Pulmonol,2005,40(5): 445–448.
EIBY Y A, WRIGHT L L, KALANJATI V P, et al. A pig model of the preterm neonate: anthropometric and physiological characteristics. PLoS One,2013,8(7): e68763[2021-08-11]. https://doi.org/10.1371/journal. pone.0068763.
HIGUCHI M, HIRANO H, MAKI M. The thromboplastic activity of lung surfactant in amniotic fluid and its application to prenatal assessment of fetal lung maturity. Tohoku J Exp Med,1981,133(3): 267–273.
MIURA T. Models of lung branching morphogenesis. J Biochem,2015, 157(3): 121–127.
MORTY R E. Recent advances in the pathogenesis of BPD. Semin Perinatol,2018,42(7): 404–412.
JENSEN E A, SCHMIDT B. Epidemiology of bronchopulmonary dysplasia. Birth Defects Res,2014,100(3): 145–157.
JOBE A H. Mechanisms of lung injury and bronchopulmonary dysplasia. Am J Perinatol,2016,33(11): 1076–1078.
SILVA D M, NARDIELLO C, POZARSKA A, et al. Recent advances in the mechanisms of lung al-veolarization and the pathogenesis of bronchopulmonary dysplasia. Am J Physiol Lung Cell Mol Physiol,2015, 309(11): 1239–1272.
NIEDERMAIER S, HILGENDORFF A. Bronchopulmonary dysplasia: An overview about pathophysiologic concepts. Mol Cell Pediatr,2015, 2(1): 2–9.
Refbacks
- There are currently no refbacks.



