Evidence map›Paper›PMID 41738294›Full record

ArticleAmerican journal of respiratory cell and molecular biology2026

Titrating cumulative neonatal hyperoxia in mice to model bronchopulmonary dysplasia severities.

Brooke Dir, Raveena Mishra, Nicole Hennen, Emily Mooers, Ru-Jeng Teng, Ganesh Konduri, Jeffrey L Segar, Justin Grobe, Matthew R Hodges, Gary C Mouradian

Abstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2026. 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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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Brooke DirDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.
Raveena MishraDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.
Nicole HennenDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.
Emily MooersDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, United States.
Ru-Jeng TengDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, United States.
Ganesh KonduriDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, United States.
Jeffrey L SegarDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.
Justin GrobeDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.
Matthew R HodgesDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.
Gary C MouradianDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.

Funding

Pulmonary vagal sensory neurons in chronic lung diseaseR01HL179101 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI Gary Charles Mouradian · 2025 to 2026
$965k
NHLBI NIH HHS R01 HL179101NHLBI NIH HHS R01HL179101NIH
6 · The paper itself

Abstract

The severity of bronchopulmonary dysplasia (BPD) is defined by the type or amount of respiratory support needed at 36 weeks' postmenstrual age, reflecting varying degrees of impairment in the supply and demand systems regulating arterial oxygenation. However, existing preclinical BPD models fail to account for the comprehensive nature of arterial oxygen regulation (lungs, control mechanisms, and metabolism). Here, based on the predictive power of cumulative supplemental oxygen and BPD severity, we demonstrate that dose-dependent increases of cumulative supplemental oxygen (CSO) limited to the saccular stage of lung development in neonatal mice underlie distinct pathophysiologic features associated with varying degrees of BPD-like phenotypes. Specifically, greater saccular-stage CSO levels elicited pathological features commonly associated with severe BPD, including worse alveolar simplification, risk for pulmonary hypertension, hypoventilation, changes in body growth, greater work of breathing, and metabolic acidosis. However, low levels of saccular-stage CSO elicited features associated with mild BPD, including mild but significant alveolar simplification and pulmonary vascular medial wall thickening, with a compensatory ventilatory hyperpnea driven by an increased neural drive to breathe. Thus, we show that different levels of CSO can elicit clinically relevant mild or severe BPD-like phenotypes, underscoring the widespread impact of CSO on physiological systems regulating arterial oxygenation. This paradigm enables preclinical testing of therapeutic efficacy across BPD severities, albeit without other common complicating factors. However, this paradigm is amenable to additional insults to align with the more complex clinical course of BPD.

Indexed as

Bronchopulmonary DysplasiaHyperoxiaAnimalsAnimals, NewbornDisease Models, AnimalHypertension, PulmonaryLungMiceMice, Inbred C57BLOxygenPulmonary AlveoliSeverity of Illness IndexOxygenbronchopulmonary dysplasia (BPD)cumulative supplemental oxygenenergy expendituremurineventilatory control

Identifiers

PMID41738294
PMCPMC13068295

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.