Evidence map›Paper›PMID 30614352›Full record

ArticleThe Journal of international medical research2019

Remote ischemic preconditioning ameliorates indirect acute lung injury by modulating phosphorylation of IκBα in mice.

Yun-Hee Kim, Young-Sung Kim, Byung-Hwa Kim, Kuen-Su Lee, Hyung-Sun Park, Choon-Hak Lim

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Remote ischemic conditioning for acute respiratory distress syndrome in COVID-19.American journal of physiology. Lung cellular and molecular physiology · 2021
    Review
  9. Review
  10. Article
  11. Involvement of Endothelin-1, HCellular and molecular neurobiology · 2019
    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

6 authors at 1 institution in 1 country.

Yun-Hee Kim1 Department of Anesthesiology and Pain Medicine, Korea University Ansan Hospital, Ansan, Korea.
Young-Sung Kim2 Department of Anesthesiology and Pain Medicine, Korea University Guro Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0001-8551-979X
Byung-Hwa Kim1 Department of Anesthesiology and Pain Medicine, Korea University Ansan Hospital, Ansan, Korea.
Kuen-Su Lee1 Department of Anesthesiology and Pain Medicine, Korea University Ansan Hospital, Ansan, Korea.
Hyung-Sun Park3 Department of Anesthesiology and Pain Medicine, Korea University Anam Hospital, Seoul, Korea.
Choon-Hak Lim3 Department of Anesthesiology and Pain Medicine, Korea University Anam Hospital, Seoul, Korea.
Korea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAcute lung injury is responsible for mortality in seriously ill patients. Previous studies have shown that systemic inflammation is attenuated by remote ischemic preconditioning (RIPC) via reducing nuclear factor-kappa B (NF-κB). Therefore, we investigated whether lipopolysaccharide (LPS)-induced indirect acute lung injury (ALI) can be protected by RIPC.

methodsRIPC was accomplished by 10 minutes of occlusion using a tourniquet on the right hind limb of mice, followed by 10 minutes of reperfusion. This process was repeated three times. Intraperitoneal LPS (20 mg/kg) was administered to induce indirect ALI. Inflammatory cytokines in bronchoalveolar lavage fluid were analyzed using an enzyme-linked immunosorbent assay. Pulmonary tissue was excised for histological examination, and for examining NF-κB activity and phosphorylation of inhibitor of κBα (IκBα).

resultsNF-κB activation and LPS-induced histopathological changes in the lungs were significantly alleviated in the RIPC group. RIPC reduced phosphorylation of IκBα in lung tissue of ALI mice.

conclusionsRIPC attenuates endotoxin-induced indirect ALI. This attenuation might occur through modification of NF-κB mediation of cytokines by modulating phosphorylation of IκBα.

Indexed as

Acute Lung InjuryAnimalsBronchoalveolar Lavage FluidCytokinesIschemic PreconditioningLipopolysaccharidesMaleMiceMice, Inbred BALB CMice, NudeNF-kappa BNF-KappaB Inhibitor alphaPhosphorylationSignal TransductionCytokinesLipopolysaccharidesNF-kappa BNF-KappaB Inhibitor alphaAcute lung injurycytokineinflammationischemic preconditioningmicesurvival rate

Identifiers

PMID30614352
PMCPMC6381478
OpenAlexW2909585193

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.