Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Hormonal regulation of alveolarization: structure-function correlation.

Samuel J Garber1, Huayan Zhang, Joseph P Foley

  • 1Division of Neonatology, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, PA, USA. garbers@email.chop.edu

Respiratory Research
|March 29, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Gut dysbiosis modulates hyperoxia-induced bronchopulmonary dysplasia by promoting EMT through activating TLR4/NF-κB pathway.

Molecular medicine (Cambridge, Mass.)·2026
Same author

Clinician Perspectives of Oxygen Control in Children With Bronchopulmonary Dysplasia at Home: An International Survey of Clinicians From 44 Countries.

Journal of paediatrics and child health·2026
Same author

Preclinical evaluation of <sup>89</sup>Zr/<sup>177</sup>Lu/<sup>161</sup>Tb-labeled anti-CD228 monoclonal antibody for theranostics in skin cutaneous melanoma.

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V·2026
Same author

A Theranostic Study of <sup>177</sup>Lu-Labeled Anti-ADAM9 Antibody for the Treatment of Triple-Negative Breast Cancer.

Bioconjugate chemistry·2026
Same author

Healthcare burden of bronchopulmonary dysplasia among very preterm infants in China: a cohort study.

BMJ paediatrics open·2026
Same author

CQMUH-011 mitigated LPS-induced acute lung injury in neonatal rabbits.

Scientific reports·2026

Dexamethasone (Dex) and all-trans-retinoic acid (RA) impact lung development differently. While RA

Area of Science:

  • Pulmonary Medicine
  • Developmental Biology
  • Neonatal Physiology

Background:

  • Dexamethasone (Dex) is known to limit alveolarization.
  • All-trans-retinoic acid (RA) is known to promote alveolarization.
  • The functional consequences of these hormonal exposures on lung development are not well understood.

Purpose of the Study:

  • To investigate the functional consequences of Dexamethasone (Dex) and all-trans-retinoic acid (RA) on neonatal rat lung development.
  • To compare the effects of individual and combined treatments with Dex and RA.
  • To assess the reversibility of treatment effects on lung structure and function.

Main Methods:

  • Neonatal rats were treated with Dex and/or RA during the first two weeks of life.
  • Morphological assessment included light microscopy and radial alveolar counts.

Related Experiment Videos

  • Functional evaluation involved plethysmography, pressure-volume curves, exercise swim testing, and arterial blood gases at various time points.
  • Main Results:

    • Dex treatment led to simplified lung architecture without secondary septation and increased lung volumes and ventilation.
    • RA treatment resulted in smaller, more numerous alveoli.
    • Concomitant Dex + RA treatment prevented Dex-induced septation changes and corrected hypercarbia, but lung volumes and function remained abnormal.
    • RA-induced structural changes were reversible after treatment cessation, unlike Dex-induced effects.

    Conclusions:

    • Both RA and corticosteroid treatments are associated with respiratory acidosis in neonates.
    • While RA-induced lung changes are reversible, Dex-induced alterations in lung function and volume persist.
    • Combined Dex + RA treatment improves septation and gas exchange but does not fully normalize pulmonary function or lung volumes.
    • These findings highlight the distinct and persistent effects of hormonal exposures on lung development.