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Updated: Apr 29, 2026

Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
Published on: October 31, 2025
Organ dysfunction among piglets treated with inhaled nitric oxide and intravenous hydrocortisone during prolonged
Sofie Paues Göranson1, Waldemar Goździk2, Piotr Harbut1
1Department of Anesthesia and Intensive Care, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
Objective:
It has previously been shown that a combination of inhaled nitric oxide (iNO) and intravenous (IV) steroid attenuates endotoxin-induced organ damage in a 6-hour porcine endotoxemia model. We aimed to further explore these effects in a 30-hour model with attention to clinically important variables.
Design:
Randomized controlled trial.
Setting:
University animal laboratory.
Subjects:
Domestic piglets (n = 30).
Interventions:
Animals were randomized into 5 groups (n = 6 each): 1) Controls, 2) LPS-only (endotoxin/lipopolysaccharide (LPS) infusion), 3) LPS + iNO, 4) LPS + IV steroid, 5) LPS + iNO + IV steroid.
Measurements And Main Results:
Exposure to LPS temporarily increased pulmonary artery mean pressure and impeded renal function with elevated serum creatinine and acidosis compared to a control group over the 30-hour study period. Double treatment with both iNO and IV steroid tended to blunt the deterioration in renal function, although the only significant effect was on Base Excess (p = 0.045). None of the LPS + iNO + IV steroid treated animals died during the study period, whereas one animal died in each of the other LPS-infused groups.
Conclusions:
This study suggests that combined early therapy with iNO and IV steroid is associated with partial protection of kidney function after 30 hours of experimental LPS infusion.
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