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Recombinant human insulin-like growth factor 1 complex preserves lung development in mechanically ventilated preterm
Kurt H Albertine1, Andrew Rebentisch1, Elaine Dawson1
1Division of Neonatology, Department of Pediatrics, University of Utah, Salt Lake City, UT, United States.
American Journal of Respiratory and Critical Care Medicine
|February 25, 2026
Summary
Recombinant human insulin-like growth factor-1 (rhIGF-1) complex improved lung development in preterm lambs. This therapy may reduce the risk of bronchopulmonary dysplasia in premature infants.
Area of Science:
- Neonatal medicine
- Pulmonary medicine
- Developmental biology
Background:
- Bronchopulmonary dysplasia is linked to low insulin-like growth factor-1 (IGF-1) in preterm infants.
- Postnatal IGF-1 replenishment is a potential strategy to prevent lung injury in premature neonates.
- Previous studies showed rhIGF-1 complex improved outcomes in preterm lambs.
Purpose of the Study:
- To assess the efficacy of a longer treatment period (7 days) with rhIGF-1 complex in younger preterm lambs.
- To evaluate the preservation of respiratory gas exchange, lung structure, and mechanics.
- To determine the safety and effectiveness of rhIGF-1 complex for lung maturation.
Main Methods:
- Mechanically ventilated preterm lambs (128d gestation) received continuous intravenous infusion of rhIGF-1 complex or saline for 7 days.
- Lambs were randomized into treatment and control groups (10 per group).
- Respiratory gas exchange, lung structure, and VEGF-R2 mRNA expression were assessed.
Main Results:
- RhIGF-1 complex significantly enhanced respiratory gas exchange and alveolar development.
- Improved alveolar capillary growth and VEGF-R2 mRNA expression were observed.
- No adverse effects on liver or kidney function were detected.
Conclusions:
- RhIGF-1 complex demonstrates potential as a safe and effective therapy for promoting lung maturation in preterm infants.
- This treatment may reduce the incidence and severity of bronchopulmonary dysplasia.
- Further research is warranted to confirm these findings in clinical settings.

