Evidence map›Paper›PMID 30728885›Full record

ArticleOxidative medicine and cellular longevity2019

Protective Effect of Ethyl Pyruvate against Myocardial Ischemia Reperfusion Injury through Regulations of ROS-Related NLRP3 Inflammasome Activation.

Ji Hae Jun, Jae-Kwang Shim, Ju Eun Oh, Eun-Jung Shin, Eunah Shin, Young-Lan Kwak

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-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

27 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  9. NormothermicFrontiers in cardiovascular medicine · 2023
    Article
  10. Article
  11. Article
  12. Ethyl pyruvate, a versatile protector in inflammation and autoimmunity.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Review
  13. Article
  14. Review
  15. Review
  16. NLRP3: Role in ischemia/reperfusion injuries.Frontiers in immunology · 2022
    Review
  17. Article
  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 1 institution in 1 country.

Ji Hae JunAnesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-8080-0715
Jae-Kwang ShimAnesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Ju Eun OhAnesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Eun-Jung ShinAnesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Eunah ShinDepartment of Pathology, CHA Gangnam Medical Center, CHA University, Seoul, Republic of Korea.
Young-Lan KwakAnesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-2984-9927
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence indicates the pronounced role of inflammasome activation linked to reactive oxygen species (ROS) in the sterile inflammatory response triggered by ischemia/reperfusion (I/R) injury. Ethyl pyruvate (EP) is an antioxidant and conveys myocardial protection against I/R injury, while the exact mechanisms remain elusive. We aimed to investigate the effect of EP on myocardial I/R injury through mechanisms related to ROS and inflammasome regulation. The rats were randomly assigned to four groups: (1) sham, (2) I/R-control (IRC), (3) EP-pretreatment + I/R, and (4) I/R + EP-posttreatment. I/R was induced by a 30 min ligation of the left anterior descending artery followed by 4 h of reperfusion. EP (50 mg/kg) was administered intraperitoneally at 1 h before ischemia (pretreatment) or upon reperfusion (posttreatment). Both pre- and post-EP treatment resulted in significant reductions in myocardial infarct size (by 34% and 31%, respectively) and neutrophil infiltration. I/R-induced myocardial expressions of NADPH oxidase-4, carnitine palmitoyltransferase 1A, and thioredoxin-interacting protein (TXNIP) were mitigated by EP. EP treatment was associated with diminished inflammasome activation (NOD-like receptor 3 (NLRP3), apoptosis-associated speck-like protein, and caspase-1) and interleukin-1

Indexed as

AnimalsHumansInflammasomesMaleMyocardial Reperfusion InjuryNLR Family, Pyrin Domain-Containing 3 ProteinPyruvatesRatsRats, Sprague-DawleyReactive Oxygen Speciesethyl pyruvateInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinPyruvatesReactive Oxygen Species

Identifiers

PMID30728885
PMCPMC6343167
OpenAlexW2910913536

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.