Evidence map›Paper›PMID 32024151›Full record

ArticleInternational journal of molecular sciences2020

Dietary Antioxidants Significantly Attenuate Hyperoxia-Induced Acute Inflammatory Lung Injury by Enhancing Macrophage Function via Reducing the Accumulation of Airway HMGB1.

Vivek Patel, Katelyn Dial, Jiaqi Wu, Alex G Gauthier, Wenjun Wu, Mosi Lin, Michael G Espey, Douglas D Thomas, Charles R Ashby, Lin L Mantell

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 73 citations in OpenAlex.

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  13. Glucosinolates and their hydrolysis products as potential nutraceuticals to combat cytokine storm in SARS-COV-2.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2022
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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

10 authors at 4 institutions in 1 country.

Vivek PatelDepartment of Pharmaceutical Sciences, College of Pharmacy, St. John's University Queens, Queens, NY 11439, USA.
Katelyn DialDepartment of Pharmaceutical Sciences, College of Pharmacy, St. John's University Queens, Queens, NY 11439, USA.
Jiaqi WuDepartment of Pharmaceutical Sciences, College of Pharmacy, St. John's University Queens, Queens, NY 11439, USA.
Alex G GauthierDepartment of Pharmaceutical Sciences, College of Pharmacy, St. John's University Queens, Queens, NY 11439, USA.
Wenjun WuDepartment of Pharmaceutical Sciences, College of Pharmacy, St. John's University Queens, Queens, NY 11439, USA.
Mosi LinDepartment of Pharmaceutical Sciences, College of Pharmacy, St. John's University Queens, Queens, NY 11439, USA.
Michael G EspeyNational Cancer Institute, Bethesda, MD 20892-9747, USA.
Douglas D ThomasDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, IL 60612, USA.
Charles R AshbyDepartment of Pharmaceutical Sciences, College of Pharmacy, St. John's University Queens, Queens, NY 11439, USA.
Lin L MantellDepartment of Pharmaceutical Sciences, College of Pharmacy, St. John's University Queens, Queens, NY 11439, USA.
St. John's University · USFeinstein Institute for Medical Research · USNational Cancer Institute · USUniversity of Illinois Chicago · US

Funding

High mobility group box 1 (HMGB1) in the airway as a therapeutic target in CFR15HL093708 · NHLBI · ST. JOHN'S UNIVERSITY · PI MANTELL, LIN L. · 2008 to 2014
$328k
NHLBI NIH HHS HL093708
6 · The paper itself

Abstract

Mechanical ventilation with hyperoxia is the major supportive measure to treat patients with acute lung injury and acute respiratory distress syndrome (ARDS). However, prolonged exposure to hyperoxia can induce oxidative inflammatory lung injury. Previously, we have shown that high levels of airway high-mobility group box 1 protein (HMGB1) mediate hyperoxia-induced acute lung injury (HALI). Using both ascorbic acid (AA, also known as vitamin C) and sulforaphane (SFN), an inducer of nuclear factor (erythroid-derived 2)-like 2 (Nrf2), we tested the hypothesis that dietary antioxidants can mitigate HALI by ameliorating HMGB1-compromised macrophage function in phagocytosis by attenuating hyperoxia-induced extracellular HMGB1 accumulation. Our results indicated that SFN, which has been shown to attenute HALI in mice exposed to hyperoxia, dose-dependently restored hyperoxia-compromised macrophage function in phagocytosis (75.9 ± 3.5% in 0.33 µM SFN versus 50.7 ± 1.8% in dimethyl sulfoxide (DMSO) control, p < 0.05) by reducing oxidative stress and HMGB1 release from cultured macrophages (47.7 ± 14.7% in 0.33 µM SFN versus 93.1 ± 14.6% in DMSO control,

Indexed as

Dietary SupplementsAcute Lung InjuryAnimalsAntioxidantsHMGB1 ProteinHyperoxiaMacrophagesMaleMiceMice, Inbred C57BLPhagocytosisPneumoniaRespiratory SystemAntioxidantsHMGB1 ProteinHMGB1 protein, mouseARDSascorbic aciddietary antioxidantsHALIHMGB1macrophagesNrf2oxidative stressphagocytosissulforaphane

Identifiers

PMID32024151
PMCPMC7037000
OpenAlexW3003826472

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.