Evidence map›Paper›PMID 27347312›Full record

ArticleAmerican journal of translational research2016

Isoflurane attenuates lipopolysaccharide-induced acute lung injury by inhibiting ROS-mediated NLRP3 inflammasome activation.

Ning Yin, Zhendan Peng, Bin Li, Jiangyan Xia, Zhen Wang, Jing Yuan, Lei Fang, Xinjiang Lu

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
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  4. Involvement of the SIRT1-NLRP3 pathway in the inflammatory response.Cell communication and signaling : CCS · 2023
    Review
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  11. Inhibitory Effects of Raw-ExtractMolecules (Basel, Switzerland) · 2020
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

8 authors at 1 institution in 1 country.

Ning YinDepartment of Anesthesiology, Zhongda Hospital, School of Medicine, Southeast University Nanjing 210009, Jiangsu, China.
Zhendan PengDepartment of Anesthesiology, Zhongda Hospital, School of Medicine, Southeast University Nanjing 210009, Jiangsu, China.
Bin LiDepartment of Anesthesiology, Zhongda Hospital, School of Medicine, Southeast University Nanjing 210009, Jiangsu, China.
Jiangyan XiaDepartment of Anesthesiology, Zhongda Hospital, School of Medicine, Southeast University Nanjing 210009, Jiangsu, China.
Zhen WangDepartment of Anesthesiology, Zhongda Hospital, School of Medicine, Southeast University Nanjing 210009, Jiangsu, China.
Jing YuanDepartment of Anesthesiology, Zhongda Hospital, School of Medicine, Southeast University Nanjing 210009, Jiangsu, China.
Lei FangDepartment of Anesthesiology, Zhongda Hospital, School of Medicine, Southeast University Nanjing 210009, Jiangsu, China.
Xinjiang LuDepartment of Anesthesiology, Zhongda Hospital, School of Medicine, Southeast University Nanjing 210009, Jiangsu, China.
Zhongda Hospital Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleotide-binding domains and leucine-rich repeat (NLR) pyrin domains containing 3 (NLRP3) inflammasome are highly involved in the pathogenesis of acute lung injury (ALI) wherein alveolar macrophages (AMs) play a crucial role. Isoflurane (ISO) has been shown to attenuate ALI. However, the inhibitory effects of ISO on NLRP3 activation in lipopolysaccharide (LPS)-induced ALI remain unknown. Here, we showed that 1.4% ISO post-treatment reduced LPS-induced body weight loss, pulmonary histopathological injury, edema, and vascular permeability in rats. ISO attenuated LPS-triggered inflammation, as evidenced by reductions in the number of total cells, neutrophils, and macrophages, and the release of IL-1β and IL-18 in the bronchoalveolar lavage fluid. ISO treatment decreased the myeloperoxidase activity, F4/80-positive cells, and the mRNA expression of IL-1β and IL-18 in the lung tissues of LPS-treated rats. Mechanistically, ISO reduced NLRP3 activation and caspase-1 activity in a reactive oxygen species (ROS)-dependent manner. An in vitro study that ISO inhibited LPS-induced AM activation partly confirmed in vivo findings. Overall, these results indicate that ISO post-conditioning alleviated LPS-induced ALI possibly by inhibiting ROS-mediated NLRP3 inflammasome activation.

Indexed as

Acute lung injuryisofluranelipopolysaccharidenucleotide-binding domain and leucine-rich repeat pyrin domain containing 3reactive oxygen species

Identifiers

PMID27347312
PMCPMC4891417
OpenAlexW2464325726

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.