Literature DB >> 30211655

Former-preterm lambs have persistent alveolar simplification at 2 and 5 months corrected postnatal age.

Mar Janna Dahl1, Sydney Bowen1, Toshio Aoki1, Andrew Rebentisch1, Elaine Dawson1, Luke Pettet1, Haleigh Emerson1, Baifeng Yu1, Zhengming Wang1, Haixia Yang1, Chong Zhang2, Angela P Presson2,3, Lisa Joss-Moore1, Donald M Null4, Bradley A Yoder1, Kurt H Albertine1.   

Abstract

Preterm birth and mechanical ventilation (MV) frequently lead to bronchopulmonary dysplasia, the histopathological hallmark of which is alveolar simplification. How developmental immaturity and ongoing injury, repair, and remodeling impact completion of alveolar formation later in life is not known, in part because of lack of suitable animal models. We report a new model, using former-preterm lambs, to test the hypothesis that they will have persistent alveolar simplification later in life. Moderately preterm lambs (~85% gestation) were supported by MV for ~6 days before being transitioned from all respiratory support to become former-preterm lambs. Results are compared with term control lambs that were not ventilated, and between males (M) and females (F). Alveolar simplification was quantified morphometrically and stereologically at 2 mo (4 M, 4 F) or 5 mo (4 M, 6 F) corrected postnatal age (cPNA) compared with unventilated, age-matched term control lambs (4 M, 4 F per control group). These postnatal ages in sheep are equivalent to human postnatal ages of 1-2 yr and ~6 yr, respectively. Multivariable linear regression results showed that former-preterm lambs at 2 or 5 mo cPNA had significantly thicker distal airspace walls ( P < 0.001 and P < 0.009, respectively), lower volume density of secondary septa ( P < 0.007 and P < 0.001, respectively), and lower radial alveolar count ( P < 0.003 and P < 0.020, respectively) compared with term control lambs. Sex-specific differences were not detected. We conclude that moderate preterm birth and MV for ~6 days impedes completion of alveolarization in former-preterm lambs. This new model provides the opportunity to identify underlying pathogenic mechanisms that may reveal treatment approaches.

Entities:  

Keywords:  alveolar capillary growth; alveolar formation; bronchopulmonary dysplasia; lung development; neonatal chronic lung disease

Mesh:

Year:  2018        PMID: 30211655      PMCID: PMC6295507          DOI: 10.1152/ajplung.00249.2018

Source DB:  PubMed          Journal:  Am J Physiol Lung Cell Mol Physiol        ISSN: 1040-0605            Impact factor:   5.464


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