Evidence map›Paper›PMID 21906671›Full record

ArticleFree radical biology & medicine2011

Omeprazole attenuates hyperoxic injury in H441 cells via the aryl hydrocarbon receptor.

Binoy Shivanna, Chun Chu, Stephen E Welty, Weiwu Jiang, Lihua Wang, Xanthi I Couroucli, Bhagavatula Moorthy

Abstract read
In one paragraph

Article in Free radical biology & medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

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  10. EndothelialAntioxidants (Basel, Switzerland) · 2021
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  15. Mice Lacking the Cytochrome P450 1B1 Gene Are Less Susceptible to Hyperoxic Lung Injury Than Wild Type.Toxicological sciences : an official journal of the Society of Toxicology · 2018
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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

7 authors at 2 institutions in 1 country.

Binoy ShivannaDivision of Neonatal–Perinatal Medicine, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX 77030, USA. shivanna@bcm.edu
Chun Chu
Stephen E Welty
Weiwu Jiang
Lihua Wang
Xanthi I Couroucli
Bhagavatula Moorthy
Texas Children's Hospital · USBaylor College of Medicine · US

Funding

MOLECULAR MECHANISMS OF CYTOCHROME P4501A1 EXPRESSIONR01ES009132 · NIEHS · BAYLOR COLLEGE OF MEDICINE · PI MOORTHY, BHAGAVATULA · 1998 to 2017
$3.8M
Role of cytochrome P4501B1 in oxygen-mediated pulmonary injuryR01ES019689 · NIEHS · BAYLOR COLLEGE OF MEDICINE · PI MOORTHY, BHAGAVATULA · 2011 to 2015
$2.1M
Molecular mechanisms of cytochrome P4501A regulation by hyperoxiaR01HL070921 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MOORTHY, BHAGAVATULA · 2004 to 2010
$2.0M
Roles of pulmonary and hepatic P4501A enzymes in hyperoxic lung injury in miceR01HL087174 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MOORTHY, BHAGAVATULA · 2007 to 2010
$1.5M
NHLBI NIH HHS HL-070921NHLBI NIH HHS HL-087174NHLBI NIH HHS R01 HL070921NHLBI NIH HHS R01 HL087174NIEHS NIH HHS ES-009132NIEHS NIH HHS ES-019689NIEHS NIH HHS R01 ES009132NIEHS NIH HHS R01 ES019689
6 · The paper itself

Abstract

Hyperoxia contributes to the development of bronchopulmonary dysplasia in premature infants. Earlier we observed that aryl hydrocarbon receptor (AhR)-deficient mice are more susceptible to hyperoxic lung injury than AhR-sufficient mice, and this phenomenon was associated with a lack of expression of cytochrome P450 1A enzymes. Omeprazole, a proton pump inhibitor used in humans with gastric acid-related disorders, activates AhR in hepatocytes in vitro. However, the effects of omeprazole on AhR activation in the lungs and its impact on hyperoxia-induced reactive oxygen species (ROS) generation and inflammation are unknown. In this study, we tested the hypothesis that omeprazole attenuates hyperoxia-induced cytotoxicity, ROS generation, and expression of monocyte chemoattractant protein-1 (MCP-1) in human lung-derived H441 cells via AhR activation. Experimental groups included cells transfected with AhR small interfering RNA (siRNA). Hyperoxia resulted in significant increases in cytotoxicity, ROS generation, and MCP-1 production, which were significantly attenuated with the functional activation of AhR by omeprazole. The protective effects of omeprazole on cytotoxicity, ROS production, and MCP-1 production were lost in H441 cells whose AhR gene was silenced by AhR siRNA. These findings support the hypothesis that omeprazole protects against hyperoxic injury in vitro via AhR activation that is associated with decreased ROS generation and expression of MCP-1.

Indexed as

Anti-Inflammatory AgentsCell Line, TumorCell SurvivalChemokine CCL2CytoprotectionEpithelial CellsGene Expression RegulationHumansHyperoxiaLungLung InjuryOmeprazoleReactive Oxygen SpeciesReceptors, Aryl HydrocarbonAnti-Inflammatory AgentsCCL2 protein, humanChemokine CCL2OmeprazoleReactive Oxygen SpeciesReceptors, Aryl Hydrocarbon

Identifiers

PMID21906671
PMCPMC3901644
OpenAlexW2039610966

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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.