Evidence map›Paper›PMID 35416858›Full record

ArticleActa cirurgica brasileira2022

Naringin attenuates acute myocardial ischemia-reperfusion injury via miR- 126/GSK-3β/β-catenin signaling pathway.

Xiuhui Guo, Qinghong Ji, Mei Wu, Weihong Ma

Open access · goldAbstract read
In one paragraph

Article in Acta cirurgica brasileira, 2022. 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
2.5field-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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  11. The role of β-catenin in cardiac diseases.Frontiers in pharmacology · 2023
    Review
  12. Regulatory role of miRNAs in Wnt signaling pathway linked with cardiovascular diseases.Current research in pharmacology and drug discovery · 2022
    Article
  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

4 authors at 1 institution in 1 country.

Xiuhui GuoMD. Department of Price Office of Finance - The Second Hospital - Cheeloo College of Medicine - Shandong University - Shandong Province, China.ORCID http://orcid.org/0000-0001-5020-6611
Qinghong JiMD. Department of Obstetrics - The Second Hospital - Cheeloo College of Medicine - Shandong University - Shandong Province, China.ORCID http://orcid.org/0000-0003-0155-0576
Mei WuMD. Department of Ultrasonography - The Second Hospital - Cheeloo College of Medicine - Shandong University - Shandong Province, China.ORCID http://orcid.org/0000-0001-8945-5965
Weihong MaMD. Department of Ultrasonography - The Second Hospital - Cheeloo College of Medicine - Shandong University - Shandong Province, China.ORCID http://orcid.org/0000-0001-5219-0967
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMyocardial ischemia-reperfusion (I/R) injury is one of the mechanisms contributing to the high mortality rate of acute myocardial infarction. PURPOSE: This study intended to study the role of naringin in cardiac I/R injury.

methodsAC16 cells (human cardiomyocyte cell line) were subjected to oxygen-glucose deprivation/recovery (OGD/R) treatment and/or naringin pretreatment. Then, the apoptosis was examined by flow cytometry and Western blotting. The concentration of IL-6, IL-8 and TNF-α was measured by enzyme-linked immunosorbent assay (ELISA) kits. How naringin influenced microRNA expression was examined by microarrays and quantitative real-time polymerase chain reaction (qRT-PCR). Dual luciferase reporter assay was employed to evaluate the interaction between miR-126 and GSK-3β. The GSK-3β/β-catenin signaling pathway was examined by Western blotting. Finally, rat myocardial I/R model was created to examine the effects of naringin in vivo.

resultsNaringin pretreatment significantly decreased the cytokine release and apoptosis of cardiomyocytes exposed to OGD/R. Bioinformatical analysis revealed that naringin upregulated miR-126 expression considerably. Also, it was found that miR-126 can bind GSK-3β and downregulate its expression, suggesting that naringin could decrease GSK-3β activity. Next, we discovered that naringin increased β-catenin activity in cardiomyocytes treated with OGD/R by inhibiting GSK-3β expression. Our animal experiments showed that naringin pre-treatment or miR-126 agomir alleviated myocardial I/R.

conclusionsNaringin preconditioning can reduce myocardial I/R injury via regulating miR-126/GSK-3β/β-catenin signaling pathway, and this chemical can be used to treat acute myocardial infarction.

Indexed as

beta CateninFlavanonesGlycogen Synthase Kinase 3 betaMicroRNAsMyocardial InfarctionMyocardial Reperfusion InjuryAnimalsApoptosisRatsSignal Transductionbeta CateninFlavanonesGlycogen Synthase Kinase 3 betaMicroRNAsMIRN126 microRNA, ratnaringin

Identifiers

PMID35416858
PMCPMC9000977
OpenAlexW4225814848

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.