Evidence map›Paper›PMID 33253607›Full record

ArticlePharmaceutical biology2020

The role of Nrf2 in astragaloside IV-mediated antioxidative protection on heart failure.

Yan-Bo Sui, Kui-Kui Zhang, Yu-Kun Ren, Li Liu, Yan Liu

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
3.5field-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

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Drug design, development and therapy · 2026
    Article
  6. Article
  7. Article
  8. Astragaloside IV Alleviates HCardiovascular therapeutics · 2025
    Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Pharmaceutical biology · 2022
    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

5 authors at 1 institution in 1 country.

Yan-Bo SuiDepartment of Cardiology, First Affiliated Hospital of Heilongjiang University of Chinese Medicine , Harbin , China.
Kui-Kui ZhangDepartment of Cardiology, First Affiliated Hospital of Heilongjiang University of Chinese Medicine , Harbin , China.
Yu-Kun RenDepartment of Dermatology, First Affiliated Hospital of Heilongjiang University of Chinese Medicine , Harbin , China.
Li LiuDepartment of Cardiology, First Affiliated Hospital of Heilongjiang University of Chinese Medicine , Harbin , China.
Yan LiuDepartment of Scientific Research Management, First Affiliated Hospital of Heilongjiang University of Chinese Medicine , Harbin , China.
First Affiliated Hospital of Heilongjiang University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextHeart failure is one of the most serious diseases worldwide. Astragaloside IV (ASI) is widely used in the treatment of cardiovascular diseases.

objectiveTo elucidate the antioxidative mechanism of ASI in a rat model of left coronary artery ligation. MATERIALS AND

methodsLeft coronary artery of Sprague-Dawley rats was ligated to establish the model of heart failure, and then vehicle (saline) or ASI (1 mg/kg/day) was orally administered to the rats (

resultsASI improved the cardiac function, especially ejection fraction (75.27 ± 5.75% vs. 36.26 ± 4.14%) and fractional shortening (45.39 ± 3.66% vs. 17.88 ± 1.32%), and reduced the infarct size of left ventricle (20.69 ± 2.98% vs. 39.11 ± 3.97%). ASI maintained the levels of glutathione, catalase and superoxide dismutase and prevented the leakage of creatine kinase. In addition, ASI induced the protein expression of Nrf2 (1.97-fold) and HO-1 (2.79-fold), while reduced that of Keap-1 (0.77-fold) in the ventricular myocardium. In H9c2 cells, a rat cardiomyocyte cell line, ASI induced the translocation of Nrf2 from cytoplasm to nucleus, followed by transcriptional activation of DISCUSSION AND

conclusionsASI prevented heart failure by counteracting oxidative stress through the Nrf2/HO-1 pathway. Application in clinical practice warrants further investigation.

Indexed as

AnimalsAntioxidantsCardiotonic AgentsCell LineEchocardiographyHeart FailureHeme Oxygenase-1MaleMyocardial InfarctionMyocytes, CardiacNF-E2-Related Factor 2Oxidative StressRatsRats, Sprague-DawleySaponinsSignal TransductionAntioxidantsastragaloside ACardiotonic AgentsHeme Oxygenase-1Nfe2l2 protein, ratNF-E2-Related Factor 2SaponinsTriterpenesHO-1Keap-1Oxidative stresstranscriptional activation

Identifiers

PMID33253607
PMCPMC7717863
OpenAlexW3108018916

What OpenQuestion holds

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LicenceCC BY
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.