Evidence map›Paper›PMID 33641489›Full record

ArticleThe Journal of international medical research2021

Atractylenolide I alleviates ischemia/reperfusion injury by preserving mitochondrial function and inhibiting caspase-3 activity.

Caiqin Sun, Xuesong Zhang, Fei Yu, Chen Liu, Fangbin Hu, Li Liu, Jing Chen, Jue Wang

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.0field-weighted citation impact, top 10% 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, 16 citations in OpenAlex.

  1. Article
  2. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Atractylenolide-I Attenuates MPTP/MPPNeurochemical research · 2024
    Article
  8. Review
  9. Review
  10. Article
  11. 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.

Caiqin SunDepartment of Cardiology, Jingjiang People's Hospital, Jingjiang, Jiangsu, P. R. China.ORCID https://orcid.org/0000-0003-1996-2763
Xuesong ZhangDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, P. R. China.
Fei YuDepartment of Cardiology, Jingjiang People's Hospital, Jingjiang, Jiangsu, P. R. China.
Chen LiuDepartment of Cardiology, Jingjiang People's Hospital, Jingjiang, Jiangsu, P. R. China.
Fangbin HuDepartment of Cardiology, Jingjiang People's Hospital, Jingjiang, Jiangsu, P. R. China.
Li LiuDepartment of Cardiology, Jingjiang People's Hospital, Jingjiang, Jiangsu, P. R. China.
Jing ChenDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, P. R. China.
Jue WangDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, P. R. China.
First People's Hospital of Jingzhou · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveMyocardial ischemia/reperfusion (I/R) injury causes various severe heart diseases, including myocardial infarction. This study aimed to determine the therapeutic effect of atractylenolide I (ATR-I), which is an active ingredient isolated from

methodsMale Sprague-Dawley rats were randomly allocated to the five following groups (nine rats/group): control, I/R, and I/R + ATR-I preconditioning (10, 50, and 250 µg). The effects of ATR-I on rats with I/R injury were verified in cardiomyocytes with hypoxia/reoxygenation. Production of reactive oxygen species was determined. The proliferative ability of cardiomyocytes was detected using the bromodeoxyuridine assay. Mitochondrial membrane potential was measured using flow cytometry. Cellular apoptosis was assessed by flow cytometry and the terminal dUTP-digoxigenin nick end labeling assay.

resultsI/R and hypoxia/reoxygenation injury increased mitochondrial dysfunction and activated caspase-3 and Bax/B cell lymphoma 2 expression

conclusionATR-I protects against I/R injury by protecting mitochondrial function and inhibiting activation of caspase-3.

Indexed as

MitochondriaMyocardial Reperfusion InjuryAnimalsApoptosisCaspase 3LactonesMaleMembrane Potential, MitochondrialMyocytes, CardiacRatsRats, Sprague-DawleyReactive Oxygen SpeciesSesquiterpenesatractylenolide ICasp3 protein, ratCaspase 3LactonesReactive Oxygen SpeciesSesquiterpenesapoptosisAtractylenolide Icaspase-3ischemia/reperfusionmitochondrial dysfunctionreactive oxygen species

Identifiers

PMID33641489
PMCPMC7923999
OpenAlexW3134810232

What OpenQuestion holds

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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.