Evidence map›Paper›PMID 41035248›Full record

ArticleClinical and experimental pediatrics2025

Ciclesonide shows a lung-protective effect in neonatal hyperoxia-exposed rats.

Victoria Mielgo, Miguel A Gomez-Solaetxe, Lara Olazar, Begoña Loureiro, Carmen Rey-Santano

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Article in Clinical and experimental pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Victoria MielgoAnimal Research Unit, BioBizkaia Health Research Institute, Barakaldo, Spain.
Miguel A Gomez-SolaetxeMedical Devices Group, University of the Basque Country (EHU), Portugalete, Spain.
Lara OlazarPerinatal Medicine Group, BioBizkaia Health Research Institute, Barakaldo, Spain.
Begoña LoureiroPerinatal Medicine Group, BioBizkaia Health Research Institute, Barakaldo, Spain.
Carmen Rey-SantanoAnimal Research Unit, BioBizkaia Health Research Institute, Barakaldo, Spain.

Funding

Instituto de Salud Carlos III PI22/00466
6 · The paper itself

Abstract

backgroundBronchopulmonary dysplasia (BPD), a chronic lung disease primarily observed in premature infants, is attributed to a lung injury-repair imbalance. Studies of postnatal corticosteroids have failed to identify clear candidates to help alleviate high BPD rates without risks or adverse effects. PURPOSE: This study aimed to assess whether the systemic postnatal administration of an alternative glucocorticoid, ciclesonide, could attenuate alterations in lung structure and right ventricular hypertrophy in a hyperoxic rat BPD-like model.

methodsIn a hyperoxia-induced model of BPD-like lung injury, pups were maintained in oxygen-enriched atmosphere-hyperoxia or normoxia (room air) for 14 days after natural birth, and subcutaneous ciclesonide (0.5 mg/kg) was administered postnatally for 5 consecutive days. On postnatal day 14, lung function (peak inspiratory pressure and compliance), lung structure (radial alveolar count, mean linear intercept, and pulmonary vessel density), and right ventricular hypertrophy were assessed.

resultsOn day 14, the effects of hyperoxia exposure were more evident in untreated rats (impaired lung compliance and structure and right ventricular hypertrophy) than in normoxia-exposed animals. Ciclesonide administration was associated with smaller body weight changes and significantly improved lung compliance, alveolarization, lung vascular growth, and right ventricular hypertrophy.

conclusionPostnatal ciclesonide administration preserved lung function and structure and prevented right ventricular hypertrophy in a hyperoxic BPD-like model. These findings suggest that postnatal ciclesonide may be an alternative to existing corticosteroids for the treatment of BPD. However, long-term studies are required to validate these findings.

Indexed as

Bronchopulmonary dysplasiaCiclesonideHyperoxia

Identifiers

PMID41035248
PMCPMC12672403

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