Evidence map›Paper›PMID 37954484›Full record

ArticleDrug design, development and therapy2023

Xingxing Li, Rongpeng Liu, Wei Liu, Xin Liu, Zongjing Fan, Jie Cui, Yang Wu, Huijun Yin, Quan Lin

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Frontiers in pharmacology · 2025
    Review
  10. ExploringJournal of inflammation research · 2025
    Article
  11. Review
  12. Review
  13. 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

9 authors at 2 institutions in 1 country.

Xingxing LiDongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, People's Republic of China.
Rongpeng LiuDongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, People's Republic of China.
Wei LiuDongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, People's Republic of China.
Xin LiuThe Third Affiliated Hospital, Beijing University of Chinese Medicine, Beijing, 100029, People's Republic of China.
Zongjing FanDongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, People's Republic of China.
Jie CuiDongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, People's Republic of China.
Yang WuDongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, People's Republic of China.
Huijun YinXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, 100091, People's Republic of China.
Quan LinDongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, People's Republic of China.
Beijing University of Chinese Medicine · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Combination of Methods: A rat model of AMI was established by ligating the left anterior descending (LAD) artery. The grouping and administration scheme were as follows: sham group, model group, PS low-dose (PS-L) group, PS high-dose (PS-H) group, PX-478 group and angiotensin converting enzyme inhibitor (ACEI) group. After 28 days of treatment, echocardiography, myocardial infarct size, some angiogenesis markers and the miR-155-5p/HIF-1α/VEGF axis were measured. Results: PS improved cardiac structure and function, reduced infarct size, and alleviated myocardial fibrosis and inflammatory cell infiltration in AMI rats. Mechanistically, PS enhanced the expression of HGF and bFGF in serum, increased the levels of MVD and CD31 in myocardial tissues, and inhibited the activation of the miR-155-5p/HIF-1α/VEGF pathway, which ultimately promoted angiogenesis. In addition, the regulatory effect of PS on angiogenesis was partly abolished by PX-478. Conclusion: PS increased the expression of MVD and CD31 in the myocardium and stimulated angiogenesis. The above effects of PS may be associated with the inhibition of the miR-155-5p/HIF-1α/VEGF axis.

Indexed as

MicroRNAsMyocardial InfarctionPanaxSalvia miltiorrhizaAnimalsHypoxia-Inducible Factor 1, alpha SubunitMustard CompoundsPhenylpropionatesRatsVascular Endothelial Growth Factor A2-amino-3-(4'-N,N-bis(2-chloroethyl)amino)phenylpropionic acid N-oxideHif1a protein, ratHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN155 microRNA, ratMustard CompoundsPhenylpropionatesVascular Endothelial Growth Factor Avascular endothelial growth factor A, ratacute myocardial infarctionangiogenesismiR-155-5p/HIF-1α/VEGFPanax quinquefolium LSalvia miltiorrhiza Bunge

Identifiers

PMID37954484
PMCPMC10638910
OpenAlexW4388424380

What OpenQuestion holds

Textmetadata
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.