Evidence map›Paper›PMID 23787115›Full record

ArticleCritical care (London, England)2013

Effect of tyrosine kinase inhibitors, imatinib and nilotinib, in murine lipopolysaccharide-induced acute lung injury during neutropenia recovery.

In Kyoung Kim, Chin Kook Rhee, Chang Dong Yeo, Hyeon Hui Kang, Dong Gun Lee, Sang Haak Lee, Jin Woo Kim

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04794088 (A Randomised, Double-blind, Placebo-controlled Study to Investigate the Safety and Efficacy of Intravenous Imatinib Mesylate), which is not on this map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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.

NCT04794088 phase2terminatednot on this mapstarted 2021, after this paper: background citation

A Randomised, Double-blind, Placebo-controlled Study to Investigate the Safety and Efficacy of Intravenous Imatinib Mesylate (Impentri®) in Subjects With Acute Respiratory Distress Syndrome Induced by COVID-19

TypeinterventionalSponsorDr. Jurjan AmanRan2021 to 2022Enrolled67ConditionsARDS, Acute Respiratory Distress Syndrome, Covid19, Endothelial DysfunctionArmsImatinib Mesylate intravenous solution, Placebo
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  16. Parkin regulates lipopolysaccharide-induced proinflammatory responses in acute lung injury.Translational research : the journal of laboratory and clinical medicine · 2017
    Article
  17. Imatinib attenuates inflammation and vascular leak in a clinically relevant two-hit model of acute lung injury.American journal of physiology. Lung cellular and molecular physiology · 2015
    Article
  18. Article
  19. Review
  20. Differential and opposing effects of imatinib on LPS- and ventilator-induced lung injury.American journal of physiology. Lung cellular and molecular physiology · 2015
    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

7 authors at 1 institution in 1 country.

In Kyoung Kim
Chin Kook Rhee
Chang Dong Yeo
Hyeon Hui Kang
Dong Gun Lee
Sang Haak Lee
Jin Woo Kim
Catholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNeutrophil recovery has been implicated in deterioration of oxygenation and exacerbation of preexisting acute lung injury (ALI). The aim of this study was to investigate whether imatinib or nilotinib was effective on lipopolysaccharide (LPS)-induced ALI during neutropenia recovery in mice.

methodsMice were rendered neutropenic with cyclophosphamide prior to the intratracheal instillation of LPS. Imatinib or nilotinib was administrated by oral gavage during neutropenia recovery. In order to study the effects of drugs, mice were killed on day 5 and blood, bronchoalveolar lavage (BAL) fluid and lung tissue samples were obtained. The lung wet/dry weight ratio and protein levels in the BAL fluid or lung tissue were determined.

resultsTreatment with imatinib or nilotinib significantly attenuated the LPS-induced pulmonary edema, and this result was supported by the histopathological examination. The concentrations of tumor necrosis factor-α, interleukin (IL)-1β, IL-6 and myeloperoxidase in BAL fluid were significantly inhibited by imatinib or nilotinib in mice of ALI during neutropenia recovery. The mRNA expressions of platelet-derived growth factor receptor-β and c-KIT in imatinib or nilotinib group were significantly lower than LPS group.

conclusionsOur data indicated that imatinib or nilotinib effectively attenuated LPS-induced ALI during neutropenia recovery. These results provide evidence for the therapeutic potential of imatinib and nilotinib in ALI during neutropenia recovery.

Indexed as

Disease Models, AnimalAcute Lung InjuryAnimalsBenzamidesFemaleImatinib MesylateLipopolysaccharidesMiceMice, Inbred ICRNeutropeniaPiperazinesProtein Kinase InhibitorsProtein-Tyrosine KinasesPyrimidinesRandom AllocationRecovery of FunctionBenzamidesImatinib MesylateLipopolysaccharidesnilotinibPiperazinesProtein Kinase InhibitorsProtein-Tyrosine KinasesPyrimidines

Identifiers

PMID23787115
PMCPMC4056323
OpenAlexW2075583450

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.