Evidence map›Paper›PMID 33523605›Full record

ArticleJournal of cellular and molecular medicine2021

Mangiferin prevents myocardial infarction-induced apoptosis and heart failure in mice by activating the Sirt1/FoxO3a pathway.

Lingli Chen, Santie Li, Jianyu Zhu, Anfu You, Xingzhou Huang, Xinchu Yi, Mei Xue

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
20.7field-weighted citation impact, top 1% 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

64 citing papers in PubMed, 121 citations in OpenAlex.

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4 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Lingli ChenDepartment of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Santie LiSchool of Pharmaceutical Science, Wenzhou Medical University, Wenzhou, China.
Jianyu ZhuDepartment of Traumatology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Anfu YouCentral Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xingzhou HuangCentral Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xinchu YiSchool of Pharmaceutical Science, Wenzhou Medical University, Wenzhou, China.
Mei XueCentral Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.ORCID 0000-0001-6273-5318
Wenzhou Medical University · CN

Funding

Science and Technology Bureau Project of Wenzhou Y20180847Science and Technology Bureau Project of Wenzhou Y20190175Science and Technology Bureau Project of Wenzhou Y2020934Zhejiang Provincial Natural Science Foundation of China LQ21H020010
6 · The paper itself

Abstract

Myocardial infarction (MI) commonly leads to cardiomyocyte apoptosis and heart failure. Mangiferin is a natural glucosylxanthone extracted from mango fruits and leaves, which has anti-apoptotic and anti-inflammatory properties in experimental cardiovascular diseases. In the present study, we investigated the role and detailed mechanism of mangiferin in MI. We used ligation of the left anterior descending coronary artery to establish an MI model in vivo, and cardiomyocyte-specific Sirt1 knockout mice were used to identify the mechanism of mangiferin. For in vitro studies, oxygen and glucose deprivation (OGD) was used to mimic ischaemia in H9c2 cardiomyocytes. In mice, mangiferin treatment increased Sirt1 expression after MI, significantly reduced the infarct area, and prevented MI-induced apoptosis and heart failure. Mangiferin reduced OGD-induced cellular apoptosis in H9c2 cells. Meanwhile, Sirt1 knockout/silencing abolished the protective effects of mangiferin. Further studies revealed that mangiferin increased FoxO3a deacetylation by up-regulating Sirt1, thus preventing apoptosis, and adenovirus-mediated constitutive acetylation of FoxO3a restricted the anti-apoptotic effects of mangiferin in vivo and in vitro. Our results indicate that mangiferin prevents cardiomyocyte apoptosis and the subsequent heart failure by activating the Sirt1/FoxO3a pathway in MI, and suggest that mangiferin may have an interesting potential in following studies towards clinical evaluation.

Indexed as

AnimalsApoptosisBiomarkersCell SurvivalDisease Models, AnimalForkhead Box Protein O3Heart FailureMiceMice, TransgenicMyocardial InfarctionMyocytes, CardiacSignal TransductionSirtuin 1XanthonesBiomarkersForkhead Box Protein O3FoxO3 protein, mousemangiferinSirt1 protein, mouseSirtuin 1XanthonesapoptosisFoxO3amangiferinmyocardial infarctionsirt1

Identifiers

PMID33523605
PMCPMC7957271
OpenAlexW3129005952

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.