Evidence map›Paper›PMID 31914698›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2020

Blockade of equilibrative nucleoside transporter 1/2 protects against Pseudomonas aeruginosa-induced acute lung injury and NLRP3 inflammasome activation.

Eboni D Chambers, Alexis White, Alexander Vang, Zhengke Wang, Alfred Ayala, Tingting Weng, Michael Blackburn, Gaurav Choudhary, Sharon Rounds, Qing Lu

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. Autophagy · 2026
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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 3 institutions in 1 country.

Eboni D ChambersVascular Research Laboratory, Providence Veterans Affairs Medical Center, Alpert Medical School of Brown University, Providence, RI, USA.
Alexis WhiteVascular Research Laboratory, Providence Veterans Affairs Medical Center, Alpert Medical School of Brown University, Providence, RI, USA.
Alexander VangVascular Research Laboratory, Providence Veterans Affairs Medical Center, Alpert Medical School of Brown University, Providence, RI, USA.
Zhengke WangVascular Research Laboratory, Providence Veterans Affairs Medical Center, Alpert Medical School of Brown University, Providence, RI, USA.
Alfred AyalaDivision of Surgical Research, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA.
Tingting WengDepartments of Biochemistry and Molecular Biology, University of Texas-Houston Medical School, Houston, TX, USA.
Michael BlackburnDepartments of Biochemistry and Molecular Biology, University of Texas-Houston Medical School, Houston, TX, USA.
Gaurav ChoudharyVascular Research Laboratory, Providence Veterans Affairs Medical Center, Alpert Medical School of Brown University, Providence, RI, USA.
Sharon RoundsVascular Research Laboratory, Providence Veterans Affairs Medical Center, Alpert Medical School of Brown University, Providence, RI, USA.
Qing LuVascular Research Laboratory, Providence Veterans Affairs Medical Center, Alpert Medical School of Brown University, Providence, RI, USA.
Brown University · USThe University of Texas Health Science Center at Houston · USRhode Island Hospital · US

Funding

Uncoupling of IL-1 beta and VEGF-A Crosstalk Contributes to Impaired Arteriogenesis Response to Ischemia in Chronic Diabetes MellitusP20GM103652 · NIGMS · OCEAN STATE RESEARCH INSTITUTE, INC. · PI HARRINGTON, ELIZABETH O · 2013 to 2022
$21.3M
TRAINING IN ENVIRONMENTAL PATHOLOGYT32ES007272 · NIEHS · BROWN UNIVERSITY · PI ZHITKOVICH, ANATOLY · 1992 to 2021
$7.5M
Mechanisms of Immune Dysfunction and Morbid Outcome in Response to Shock/SepsisR35GM118097 · NIGMS · RHODE ISLAND HOSPITAL · PI AYALA, ALFRED · 2016 to 2025
$6.3M
CFlm25 mediated alternative polyadenylation regulates fibrosis in systemic sclerosisR01AR073284 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ASSASSI, SHERVIN, MILLS, TINGTING WENG · 2019 to 2023
$1.7M
Nicotinic Acetylcholine Receptors and RV Dysfunction in Pulmonary HypertensionR01HL128661 · NHLBI · OCEAN STATE RESEARCH INSTITUTE, INC. · PI CHOUDHARY, GAURAV · 2015 to 2018
$1.3M
HDAC6 regulates cigarette smoke-induced endothelial barrier dysfunction and lung injuryR01HL130230 · NHLBI · OCEAN STATE RESEARCH INSTITUTE, INC. · PI ROUNDS, SHARON IRENE SMITH · 2016 to 2019
$1.3M
Mechanisms of Cigarette Smoke-Induced Acute Lung InjuryI01BX002622 · VA · PROVIDENCE VA MEDICAL CENTER · PI ROUNDS, SHARON IRENE SMITH · 2015 to 2020
–
BLRD VA I01 BX002622NHLBI NIH HHS R01 HL128661NHLBI NIH HHS R01 HL130230NIAMS NIH HHS R01 AR073284NIEHS NIH HHS T32 ES007272NIGMS NIH HHS P20 GM103652NIGMS NIH HHS R35 GM118097
6 · The paper itself

Abstract

Pseudomonas aeruginosa infections are increasingly multidrug resistant and cause healthcare-associated pneumonia, a major risk factor for acute lung injury (ALI)/acute respiratory distress syndrome (ARDS). Adenosine is a signaling nucleoside with potential opposing effects; adenosine can either protect against acute lung injury via adenosine receptors or cause lung injury via adenosine receptors or equilibrative nucleoside transporter (ENT)-dependent intracellular adenosine uptake. We hypothesized that blockade of intracellular adenosine uptake by inhibition of ENT1/2 would increase adenosine receptor signaling and protect against P. aeruginosa-induced acute lung injury. We observed that P. aeruginosa (strain: PA103) infection induced acute lung injury in C57BL/6 mice in a dose- and time-dependent manner. Using ENT1/2 pharmacological inhibitor, nitrobenzylthioinosine (NBTI), and ENT1-null mice, we demonstrated that ENT blockade elevated lung adenosine levels and significantly attenuated P. aeruginosa-induced acute lung injury, as assessed by lung wet-to-dry weight ratio, BAL protein levels, BAL inflammatory cell counts, pro-inflammatory cytokines, and pulmonary function (total lung volume, static lung compliance, tissue damping, and tissue elastance). Using both agonists and antagonists directed against adenosine receptors A

Indexed as

Acute Lung InjuryAnimalsEquilibrative Nucleoside Transporter 1Equilibrative-Nucleoside Transporter 2InflammasomesMaleMiceNLR Family, Pyrin Domain-Containing 3 ProteinPseudomonas aeruginosaPseudomonas InfectionsThioinosine4-nitrobenzylthioinosineEquilibrative Nucleoside Transporter 1Equilibrative-Nucleoside Transporter 2InflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseSLC29A1 protein, mouseSlc29a2 protein, mouseThioinosineacute lung injuryequilibrative nucleoside transportersNLRP3 inflammasomepneumoniaPseudomonas aeruginosa

Identifiers

PMID31914698
PMCPMC7045807
OpenAlexW2992662863

What OpenQuestion holds

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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.