Postnatal growth restriction impairs rat lung structure and function

• Published in: Anatomical record (Hoboken, N.J. : 2007)
• Main Authors: Zhao, James, Ballard, Craig, Cohen, Adrienne J, Ringham, Ben, Zhao, Brooke, Wang, Haimei, Zuspan, Katie, Rebentisch, Andrew, Locklear, Brent A, Dahl, MarJanna, Maschek, J Alan, Cox, James E, Joss-Moore, Lisa A
• Format: Journal Article
• Language: English
• Published: United States 28.07.2023
• Subjects: preterm; lung disease; growth restriction; lung development
• ISSN: 1932-8486; 1932-8494
• DOI: 10.1002/ar.25297

The negative impact of nutritional deficits in the development of bronchopulmonary dysplasia is well recognized, yet mechanisms by which nutrition alters lung outcomes and nutritional strategies that optimize development and protect the lung remain elusive. Here, we use a rat model to assess the isolated effects of postnatal nutrition on lung structural development without concomitant lung injury. We hypothesize that postnatal growth restriction (PGR) impairs lung structure and function, critical mediators of lung development, and fatty acid profiles at postnatal day 21 in the rat. Rat pups were cross-fostered at birth to rat dams with litter sizes of 8 (control) or 16 (PGR). Lung structure and function, as well as serum and lung tissue fatty acids, and lung molecular mediators of development, were measured. Male and female PGR rat pups had thicker airspace walls, decreased lung compliance, and increased tissue damping. Male rats also had increased lung elastance, increased lung elastin protein abundance, and lysol oxidase expression, and increased elastic fiber deposition. Female rat lungs had increased conducting airway resistance and reduced levels of docosahexaenoic acid in lung tissue. We conclude that PGR impairs lung structure and function in both male and female rats, with sex-divergent changes in lung molecular mediators of development.