Evidence map›Paper›PMID 40320974›Full record

ArticleThe Journal of physiology2025

Hypoxic pregnancy promotes fibrosis and increases stress metabolites in the ovine fetal liver.

Molly M McGuckin, Dong Wang, Jasmine Ortiz, Evgenia Dobrinskikh, Wen Tong, Kimberley J Botting-Lawford, Youguo Niu, Dino A Giussani, Stephanie R Wesolowski

Abstract read
In one paragraph

Article in The Journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Review
  2. Fetal nutrient flux and oxidative metabolism during hypoxia: adaptive responses to defend fetal growth.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Molly M McGuckinDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.ORCID 0000-0002-2181-9213
Dong WangDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Jasmine OrtizDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Evgenia DobrinskikhDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Wen TongDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Kimberley J Botting-LawfordDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Youguo NiuDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID 0000-0002-8843-9952
Dino A GiussaniDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID 0000-0002-1308-1204
Stephanie R WesolowskiDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.ORCID 0000-0001-7523-0394

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI BRYAN C BERGMAN · 1995 to 2026
$32.6M
University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Maki Nakayama · 2020 to 2026
$10.8M
Training Program in Perinatal Biology and MedicineT32HD007186 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Paul Joseph Rozance · 1985 to 2026
$6.5M
Effects of chronic hypoxia and AMPK activation on uteroplacental perfusion, placental metabolism and the regulation of fetal growthR01HD088590 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Colleen Glyde Julian, LORNA G. MOORE · 2016 to 2026
$4.3M
Nutrient and Insulin Metabolic Actions in IUGR Fetal LiverR01DK108910 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Stephanie R Wesolowski · 2017 to 2026
$4.3M
Intrauterine mechanisms for liver metabolic disease in the growth-restricted fetusF32DK139657 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MCGUCKIN, MOLLY · 2024 to 2025
$137k
NCI NIH HHS P30 CA046934NICHD NIH HHS R01 HD088590NICHD NIH HHS T32 HD007186NIDDK NIH HHS F32 DK139657NIDDK NIH HHS P30 DK048520NIDDK NIH HHS P30 DK116073NIDDK NIH HHS R01 DK108910
6 · The paper itself

Abstract

Fetal chronic hypoxia is a common pregnancy complication associated with fetal growth restriction. Growth-restricted offspring have a higher risk for liver metabolic disease. Our objective was to better understand how chronic hypoxia impacts the developing fetal liver. We hypothesized that hypoxia promotes hepatocellular injury, shifts nutrient metabolism, and activates energetic and oxidative stress in the fetal liver. We used an ovine model of chronic hypoxia where pregnant ewes were housed under normoxic (CON) or hypoxic (HOX) conditions for 30 days in late gestation. Fetal liver was obtained, histologically analysed and profiled using bulk-RNA sequencing and metabolomics. Nutrient and oxidative stress signalling pathways were also measured. HOX fetuses had greater hepatic periportal collagen deposition. Metabolomics and transcriptomics predicted disruptions in central carbon metabolism, mitochondrial dysfunction and decreased oxidative phosphorylation. In support, we found potentiation of the gluconeogenic pathway and increased lactate production, pyruvate oxidation and AMPK activation. By contrast to the predicted effects, hypoxic livers maintained mitochondrial oxidation and antioxidant capacity. Interestingly, acylcarnitines were increased, yet hepatic triglyceride content was similar. Although there was little activation of oxidative stress markers, such as lipid peroxidation or oxidized glutathione, we uncovered a unique profile of liver stress-related metabolites in association with periportal collagen. Thus, hypoxic pregnancy increased fetal hepatic collagen deposition, indicating liver injury, in association with a unique profile of liver stress metabolites and adaptations in central carbon metabolism. These results provide new insight into how chronic fetal hypoxia may initiate fibrotic and metabolic liver disease risk in offspring of adverse pregnancy. KEY POINTS: Chronic exposure to hypoxic pregnancy increased fetal hepatic collagen deposition, indicating hepatocellular injury. Hypoxic fetal livers had a unique profile of stress metabolites and adaptations in central carbon metabolism. This provides new insight into how hypoxia, a common pregnancy complication associated with fetal growth restriction, may initiate fibrotic and metabolic liver disease risk.

Indexed as

Fetal HypoxiaHypoxiaLiverLiver CirrhosisAnimalsFemaleOxidative StressPregnancySheepfetalhypoxemiametabolism

Identifiers

PMID40320974
PMCPMC12126611

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Registered trials

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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.