Evidence map›Paper›PMID 26191153›Full record

ArticleInternational journal of clinical and experimental pathology2015

Rapamycin reverses paraquat-induced acute lung injury in a rat model through inhibition of NFκB activation.

Da Chen, Tao Ma, Xiao-Wei Liu, Chen Yang, Zhi Liu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.7field-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

16 citing papers in PubMed, 21 citations in OpenAlex.

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  11. The Role of Autophagy and the Chemokine (C-X-C Motif) Ligand 16 During Acute Lung Injury in Mice.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  12. Article
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  15. Role of Nrf2 and Autophagy in Acute Lung Injury.Current pharmacology reports · 2016
    Article
  16. 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

5 authors at 1 institution in 1 country.

Da ChenDepartment of Emergency, The First Affiliated Hospital of China Medical University Shenyang 110001, P. R. China.
Tao MaDepartment of Emergency, The First Affiliated Hospital of China Medical University Shenyang 110001, P. R. China.
Xiao-Wei LiuDepartment of Emergency, The First Affiliated Hospital of China Medical University Shenyang 110001, P. R. China.
Chen YangDepartment of Emergency, The First Affiliated Hospital of China Medical University Shenyang 110001, P. R. China.
Zhi LiuDepartment of Emergency, The First Affiliated Hospital of China Medical University Shenyang 110001, P. R. China.
First Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the role of rapamycin (RAPA) in paraquat (PQ)-induced acute lung injury.

methodsLung tissues were stained with HE and lung histology was observed. Mortality rate, and neutrophil and leukocyte count in blood and bronchoalveolar lavage fluid (BALF) were recorded. Protein content in BALF was determined by Coomassie blue staining. Malondialdehyde (MDA) content, glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) activity in blood were determined by thiobarbituric acid (TBA) assay, pyrogallol autoxidation method, and modified Haefman method, respectively. The NF-κB activity was measured by gel electrophoretic mobility shift assay (EMSA). Carbon dioxide partial pressure (PaCO2), partial pressure of oxygen (PaO2) and pH values were measured by automated blood gas analyzer.

resultsHE staining results demonstrated RAPA alleviated pathological changes of acute alveolitis in SD rats. Trend of protein content in BALF was PQ group>RAPA treatment group>control group (P<0.05). Neutrophil and leukocyte count in RAPA treatment group was significantly lower than PQ group at 3, 5, and 7 days after injection (P<0.05). Trend of MDA content was RAPA treatment group>PQ group>control group (P<0.05). Trend of GSH-Px and SOD activity was control group>RAPA treatment group>PQ group (P<0.05). Compared with PQ group, PaO2 in RAPA treatment group was markedly higher and PaCO2 was lower (P<0.05).

conclusionPQ-induced acute lung injury was effectively reversed with RAPA, through inhibition of NF-κB activation.

Indexed as

Acute Lung InjuryAnimalsBiomarkersBronchoalveolar Lavage FluidCarbon DioxideDisease Models, AnimalGlutathione PeroxidaseHydrogen-Ion ConcentrationLungMaleMalondialdehydeNeutrophilsNF-kappa Bp38 Mitogen-Activated Protein KinasesParaquatPhosphorylationBiomarkersCarbon DioxideGlutathione PeroxidaseMalondialdehydeNF-kappa Bp38 Mitogen-Activated Protein KinasesParaquatSirolimusSuperoxide Dismutaseacute lung injuryglutathione peroxidasemalondialdehydeNF-κBparaquatparaquat-induced acute lung injury rat modelRapamycinsuperoxide dismutase

Identifiers

PMID26191153
PMCPMC4503025
OpenAlexW2414746581

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.