Evidence map›Paper›PMID 26788251›Full record

ArticleOxidative medicine and cellular longevity2016

Cardioprotective Effects of Astragalin against Myocardial Ischemia/Reperfusion Injury in Isolated Rat Heart.

Daoxu Qu, Jichun Han, Huanhuan Ren, Wenxiao Yang, Xinjie Zhang, Qiusheng Zheng, Dong Wang

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 74 citations in OpenAlex.

  1. Chinese medical journal · 2018
    Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Molecules (Basel, Switzerland) · 2024
    Article
  8. Review
  9. Astragalin and Isoquercitrin Isolated fromFoods (Basel, Switzerland) · 2022
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Compounds Isolated fromFrontiers in pharmacology · 2021
    Article
  18. Article
  19. Review
  20. 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

7 authors at 3 institutions in 1 country.

Daoxu QuDepartment of Cardiac Surgery, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan 250014, China.
Jichun HanKey Laboratory of Xinjiang Endemic Phytomedicine Resources, Ministry of Education, Pharmacy School, Shihezi University, Shihezi 832002, China.ORCID 0000-0002-2650-0519
Huanhuan RenKey Laboratory of Xinjiang Endemic Phytomedicine Resources, Ministry of Education, Pharmacy School, Shihezi University, Shihezi 832002, China.
Wenxiao YangShandong University of Traditional Chinese Medicine, Jinan 250014, China.
Xinjie ZhangDepartment of Cardiac Surgery, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan 250014, China.
Qiusheng ZhengKey Laboratory of Xinjiang Endemic Phytomedicine Resources, Ministry of Education, Pharmacy School, Shihezi University, Shihezi 832002, China.
Dong WangDepartment of Cardiac Surgery, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan 250014, China.
Shandong University · CNShihezi University · CNShandong University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aims to evaluate the cardioprotective effects of astragalin against myocardial ischemia/reperfusion (I/R) injury in isolated rat heart. The cardioprotective effects of astragalin on myocardial I/R injury were investigated on Langendorff apparatus. Adult male Sprague-Dawley rats were randomly divided into five groups. The results showed that astragalin pretreatment improved myocardial function. Compared with I/R group, lactate dehydrogenase (LDH) and creatine kinase (CK) activities in coronary flow decreased in astragalin pretreatment groups, whereas superoxide dismutase (SOD) activity and glutathione/glutathione disulfide (GSH/GSSG) ratio significantly increased. The levels of malondialdehyde (MDA), intracellular reactive oxygen species (ROS), tumor necrosis factor-α (TNF-α), and interleukin-6 (IL-6) decreased in astragalin-treated groups. The infarct size (IS) and apoptosis rate in hearts from astragalin-treated groups were lower than those in hearts from the I/R group. Western blot analysis also revealed that astragalin preconditioning significantly reduced Bax level, whereas Bcl-2 was increased in the myocardium. Therefore, astragalin exhibited cardioprotective effects via its antioxidative, antiapoptotic, and anti-inflammatory activities.

Indexed as

AnimalsApoptosisbcl-2-Associated X ProteinBlotting, WesternCardiotonic AgentsCoronary CirculationGlutathioneHeartHeart Function TestsHeart VentriclesInflammationIn Vitro TechniquesKaempferolsMaleMalondialdehydeMyocardial Infarctionastragalinbcl-2-Associated X ProteinCardiotonic AgentsGlutathioneKaempferolsMalondialdehydeSuperoxide Dismutase

Identifiers

PMID26788251
PMCPMC4695676
OpenAlexW2207554414

What OpenQuestion holds

Textmetadata
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.