Evidence map›Paper›PMID 31205936›Full record

ArticleBioMed research international2019

Mitochondrial Division Inhibitor 1 Attenuates Mitophagy in a Rat Model of Acute Lung Injury.

Xu Luo, Ruimeng Liu, Zhihao Zhang, Zhugui Chen, Jian He, Youtan Liu

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.4field-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.

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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Advances in understanding mitophagy's role in lung injury.Chinese journal of traumatology = Zhonghua chuang shang za zhi · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. The mitophagy pathway and its implications in human diseases.Signal transduction and targeted therapy · 2023
    Review
  11. Attenuation of PMParticle and fibre toxicology · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. Article
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  17. Review
  18. Article
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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

6 authors at 4 institutions in 1 country.

Xu LuoDepartment of Critical Care Medicine, People's Hospital of Longhua, Shenzhen 518109, China.
Ruimeng LiuDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen 518110, China.ORCID 0000-0002-6720-4660
Zhihao ZhangDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen 518110, China.ORCID 0000-0002-6342-3049
Zhugui ChenDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524023, China.ORCID 0000-0002-3419-7089
Jian HeDepartment of Anesthesiology, The First People's Hospital of Foshan, Foshan 528000, China.ORCID 0000-0001-7240-1194
Youtan LiuDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen 518110, China.ORCID 0000-0003-2916-2073
Southern Medical University Shenzhen Hospital · CNFirst People's Hospital of Foshan · CNGuangdong Medical College · CNShenZhen People’s Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The regulation of intracellular mitochondria degradation is mediated by mitophagy. While studies have shown that mitophagy can lead to mitochondrial dysfunction and cell damage, the role of Mdivi-1 and mitophagy remains unclear in acute lung injury (ALI) pathogenesis. In this study, we demonstrated that Mdivi-1, which is widely used as an inhibitor of mitophagy, ameliorated acute lung injury assessed by HE staining, pulmonary microvascular permeability assay, measurement of wet/dry weight (W/D) ratio, and oxygenation index (PaO2/FiO2) analysis. Then, the mitophagy related proteins were evaluated by western blot. The results indicated that LPS-induced activation of mitophagy was inhibited by Mdivi-1 treatment. In addition, we found that Mdivi-1 protected A549 cells against LPS-induced mitochondrial dysfunction. We also found that Mdivi-1 reduced pulmonary cell apoptosis in the LPS-challenged rats and protected pulmonary tissues from oxidative stress (represented by the content of superoxide dismutase, malondialdehyde and lipid peroxides in lung). Moreover, Mdivi-1 treatment ameliorated LPS-induced lung inflammatory response and cells recruitment. These findings indicate that Mdivi-1 mitigates LPS-induced apoptosis, oxidative stress, and inflammation in ALI, which may be associated with mitophagy inhibition. Thus, the inhibition of mitophagy may represent a potential therapy for treating ALI.

Indexed as

A549 CellsAcute Lung InjuryAnimalsApoptosisDisease Models, AnimalHumansLipopolysaccharidesMaleMitochondriaMitophagyOxidative StressQuinazolinonesRatsRats, Sprague-Dawley3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinoneLipopolysaccharidesQuinazolinones

Identifiers

PMID31205936
PMCPMC6530225
OpenAlexW2943898851

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.