Evidence map›Paper›PMID 26047641›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2015

Metformin attenuates hyperoxia-induced lung injury in neonatal rats by reducing the inflammatory response.

Xueyu Chen, Frans J Walther, Rozemarijn M A Sengers, El Houari Laghmani, Asma Salam, Gert Folkerts, Tonio Pera, Gerry T M Wagenaar

Abstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Metformin Promotes Angiogenesis in Neonatal Lung Injury: A New Deal of an Old Drug.American journal of respiratory cell and molecular biology · 2024
    Article
  4. Article
  5. Article
  6. AMPK Activation: Respiratory Panacea?American journal of respiratory cell and molecular biology · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. PD 102807 Induces M3 mAChR-Dependent GRK-/Arrestin-Biased Signaling in Airway Smooth Muscle Cells.American journal of respiratory cell and molecular biology · 2022
    Article
  11. Diabetes and COVID-19: Short- and Long-Term Consequences.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2022
    Review
  12. Review
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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

8 authors at 3 institutions in 2 countries.

Xueyu ChenDepartment of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands;
Frans J WaltherDepartment of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands; Department of Pediatrics, Los Angeles Biomedical Research Institute at Harbor-University of California, Los Angeles Medical Center, Torrance, California;
Rozemarijn M A SengersDepartment of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands;
El Houari LaghmaniDepartment of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands;
Asma SalamDepartment of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands;
Gert FolkertsDepartment of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands; and.
Tonio PeraDepartment of Pulmonology, Leiden University Medical Center, Leiden, The Netherlands.
Gerry T M WagenaarDepartment of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands; g.t.m.wagenaar@lumc.nl.
Leiden University Medical Center · NLThe Lundquist Institute · USUtrecht University · NL

Funding

Synthetic Lung Surfactant Optimized for Biomedical ApplicationR01HL092158 · NHLBI · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI WALTHER, FRANCISKUS JOHANNES · 2008 to 2011
$1.3M
Synthetic surfactant and toxic chemical lung injuryR01ES015330 · NIEHS · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI WALTHER, FRANCISKUS JOHANNES · 2008 to 2011
$1.2M
NHLBI NIH HHS 1R01-HL-092158NHLBI NIH HHS R01 HL092158NIEHS NIH HHS 1R01-ES-015330
6 · The paper itself

Abstract

Because therapeutic options are lacking for bronchopulmonary dysplasia (BPD), there is an urgent medical need to discover novel targets/drugs to treat this neonatal chronic lung disease. Metformin, a drug commonly used to lower blood glucose in type 2 diabetes patients, may be a novel therapeutic option for BPD by reducing pulmonary inflammation and fibrosis and improving vascularization. We investigated the therapeutic potential of daily treatment with 25 and 100 mg/kg metformin, injected subcutaneously in neonatal Wistar rats with severe experimental BPD, induced by continuous exposure to 100% oxygen for 10 days. Parameters investigated included survival, lung and heart histopathology, pulmonary fibrin and collagen deposition, vascular leakage, right ventricular hypertrophy, and differential mRNA expression in the lungs of key genes involved in BPD pathogenesis, including inflammation, coagulation, and alveolar development. After daily metformin treatment rat pups with experimental BPD had reduced mortality, alveolar septum thickness, lung inflammation, and fibrosis, demonstrated by a reduced influx of macrophages and neutrophils and hyperoxia-induced collagen III and fibrin deposition (25 mg/kg), as well as improved vascularization (100 mg/kg) compared with control treatment. However, metformin did not ameliorate alveolar enlargement, small arteriole wall thickening, vascular alveolar leakage, and right ventricular hypertrophy. In conclusion metformin prolongs survival and attenuates pulmonary injury by reducing pulmonary inflammation, coagulation, and fibrosis but does not affect alveolar development or prevent pulmonary arterial hypertension and right ventricular hypertrophy in neonatal rats with severe hyperoxia-induced experimental BPD.

Indexed as

AnimalsAnimals, NewbornAnti-Inflammatory AgentsBronchopulmonary DysplasiaCapillary PermeabilityCollagenDose-Response Relationship, DrugDrug Evaluation, PreclinicalElastinFibrinGene ExpressionHypertrophy, Right VentricularLungMetforminRats, WistarAnti-Inflammatory AgentsCollagenElastinFibrinMetforminbronchopulmonary dysplasiacoagulationfibrosislung inflammation

Identifiers

PMID26047641
PMCPMC4525117
OpenAlexW2272943446

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.