Evidence map›Paper›PMID 28176247›Full record

ArticleMolecular and cellular biochemistry2017

Apigenin alleviates STZ-induced diabetic cardiomyopathy.

Huang-Jun Liu, Yun-Lin Fan, Hai-Han Liao, Yuan Liu, Si Chen, Zhen-Guo Ma, Ning Zhang, Zheng Yang, Wei Deng, Qi-Zhu Tang

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed, 56 citations in OpenAlex.

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  8. Exploring the Antidiabetic Potential ofPlants (Basel, Switzerland) · 2024
    Article
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  11. Hypoglycemic and hypolipidemic effects ofFood science & nutrition · 2024
    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

10 authors at 4 institutions in 1 country.

Huang-Jun LiuDepartment of Cardiology, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, China.
Yun-Lin FanDepartment of Cardiology, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, China.
Hai-Han LiaoDepartment of Cardiology, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, China.
Yuan LiuDepartment of Cardiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Si ChenCollege of Pharmacy, Hubei University of Science and Technology, Xianning, China.
Zhen-Guo MaDepartment of Cardiology, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, China.
Ning ZhangDepartment of Cardiology, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, China.
Zheng YangDepartment of Cardiology, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, China.
Wei DengDepartment of Cardiology, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, China.
Qi-Zhu TangDepartment of Cardiology, Renmin Hospital of Wuhan University, Jiefang Road 238, Wuhan, 430060, China. qztang@whu.edu.cn.
Wuhan University · CNRenmin Hospital of Wuhan University · CNFirst Affiliated Hospital of Zhengzhou University · CNHubei University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apigenin is an important component of fruits and vegetables in human daily diets. Several cellular and animal models have been performed to demonstrate its anti-oxidant and anti-inflammatory bioactivities. However, the cardioprotective effects of apigenin in diabetic cardiomyopathy (DCM) remain unclear. In this study, we intended to explore the roles of apigenin in cardiac remodeling of DCM. Male C57BL/6 J mice were treated with streptozotocin (STZ, 50 mg/kg) for 5 consecutive days to induce DCM. The echocardiography and catheter-based measurements of hemodynamic parameters were performed to evaluate the cardiac function. Paraffin slices of harvested hearts were prepared for histological pathological analysis and TUNEL assay. Oxidative assay kits were used to detect Glutathione Peroxidase (GPx), Lipid Peroxidation Malondialdehyde (MDA), and Superoxide Dismutase (SOD). Western blot and real-time PCR were used for accessing the expressions of protein and mRNA. Diabetes mellitus exacerbated the cardiac dysfunction, fibrosis, and overaccumulation of 4-hydroxynonenal accompanying with down-regulation of Bcl2, GPx, and SOD, up-regulation of MDA, cleaved caspase3, and pro-apoptotic protein Bax, and contribution to the translocation of NF-κB. All these pathological changes could be effectively blunted by treatment of apigenin in vivo. Finally, H9c2 treated with high glucose or apigenin was used for further investigation of these effects in vitro; what is more, we also compared the effects between apigenin and Resveratrol in in vitro experiments. Our experiments have demonstrated that apigenin may be a potential drug for diabetic patients suffering from DCM.

Indexed as

AnimalsAntioxidantsApigeninCardiotonic AgentsCell LineDiabetic CardiomyopathiesGene Expression RegulationHumansLipid PeroxidationMaleMiceMice, Inbred C57BLRatsResveratrolStilbenesStreptozocinAntioxidantsApigeninCardiotonic AgentsResveratrolStilbenesStreptozocinApigeninApoptosisDiabetic cardiomyopathyInflammationOxidative stress

Identifiers

PMID28176247
OpenAlexW2587300754

What OpenQuestion holds

Textmetadata
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.