Evidence map›Paper›PMID 27819271›Full record

ArticleScientific reports2016

Water-soluble acacetin prodrug confers significant cardioprotection against ischemia/reperfusion injury.

Hui Liu, Lei Yang, Hui-Jun Wu, Kui-Hao Chen, Feng Lin, Gang Li, Hai-Ying Sun, Guo-Sheng Xiao, Yan Wang, Gui-Rong Li

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  8. Article
  9. Review
  10. Metabolites Analysis of Anti-Myocardial Ischemia Active Components ofInternational journal of molecular sciences · 2022
    Article
  11. Acacetin as a Potential Protective Compound against Cardiovascular Diseases.Evidence-based complementary and alternative medicine : eCAM · 2022
    Review
  12. Effects of Lycopene Attenuating Injuries in Ischemia and Reperfusion.Oxidative medicine and cellular longevity · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Acacetin Suppresses IL-1BioMed research international · 2020
    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

10 authors at 4 institutions in 2 countries.

Hui LiuDepartment of Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, China.
Lei YangDepartment of Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, China.
Hui-Jun WuDepartment of Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, China.
Kui-Hao ChenDepartment of Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, China.
Feng LinShanghai Institute of Pharmaceutical Industry, China National Pharmaceutical Group, Shanghai, China.
Gang LiDepartment of Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, China.
Hai-Ying SunDepartment of Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, China.
Guo-Sheng XiaoXiamen Cardiovascular Hospital, Medical College of Xiamen University, Xiamen, Fujian, China.
Yan WangXiamen Cardiovascular Hospital, Medical College of Xiamen University, Xiamen, Fujian, China.
Gui-Rong LiDepartment of Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, China.
University of Hong Kong · HKXiamen University · CNShanghai Institute of Pharmaceutical Industry · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The morbidity and mortality of patients with ischemic cardiomyopathy resulted from ischemia/reperfusion injury are very high. The present study investigates whether our previously synthesized water-soluble phosphate prodrug of acacetin was cardioprotective against ischemia/reperfusion injury in an in vivo rat model. We found that intravenous administration of acacetin prodrug (10 mg/kg) decreased the ventricular arrhythmia score and duration, reduced ventricular fibrillation and infarct size, and improved the impaired heart function induced by myocardial ischemia/reperfusion injury in anesthetized rats. The cardioprotective effects were further confirmed with the parent compound acacetin in an ex vivo rat regional ischemia/reperfusion heart model. Molecular mechanism analysis revealed that acacetin prevented the ischemia/reperfusion-induced reduction of the anti-oxidative proteins SOD-2 and thioredoxin, suppressed the release of inflammation cytokines TLR4, IL-6 and TNFα, and decreased myocyte apoptosis induced by ischemia/reperfusion. Our results demonstrate the novel evidence that acacetin prodrug confer significant in vivo cardioprotective effect against ischemia/reperfusion injury by preventing the reduction of endogenous anti-oxidants and the release of inflammatory cytokines, thereby inhibiting cardiomyocytes apoptosis, which suggests that the water-soluble acacetin prodrug is likely useful in the future as a new drug candidate for treating patients with acute coronary syndrome.

Indexed as

AnimalsApoptosisDisease Models, AnimalFlavonesHeartHeart RateInterleukin-6MaleModels, BiologicalMyocardial InfarctionMyocardial Reperfusion InjuryMyocardiumOxidative StressProdrugsProtective AgentsRatsacacetinFlavonesInterleukin-6ProdrugsProtective AgentsSuperoxide DismutaseSuperoxide Dismutase 2ThioredoxinsToll-Like Receptor 4Tumor Necrosis Factor-alpha

Identifiers

PMID27819271
PMCPMC5098248
OpenAlexW2552022555

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.