Evidence map›Paper›PMID 35081907›Full record

ArticleBMC cardiovascular disorders2022

Resveratrol ameliorates myocardial fibrosis by regulating Sirt1/Smad3 deacetylation pathway in rat model with dilated cardiomyopathy.

Qingquan Chen, Yu Zeng, Xiulin Yang, Yue Wu, Shuyu Zhang, Shirong Huang, Yameng Zhong, Min Chen

Open access · goldAbstract read
In one paragraph

Article in BMC cardiovascular disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  11. Acetylation in Cardiac Aging: Molecular Mechanism and Therapeutic Approaches.Results and problems in cell differentiation · 2025
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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

8 authors at 4 institutions in 1 country.

Qingquan ChenDepartment of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, 88 Jiaotong Road, Fuzhou, 350004, Fujian, China. cqq036@126.com.
Yu ZengXiamen Maternal and Pediatric Hospital, Women and Children's Hospital Affiliated To Xiamen University, Xiamen, 361003, China.
Xiulin YangDepartment of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, 88 Jiaotong Road, Fuzhou, 350004, Fujian, China.
Yue WuDepartment of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, 88 Jiaotong Road, Fuzhou, 350004, Fujian, China.
Shuyu ZhangDepartment of Laboratory Medicine, Fujian Obstetrics and Gynecology Hospital, Fuzhou, 350012, China.
Shirong HuangDepartment of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, 88 Jiaotong Road, Fuzhou, 350004, Fujian, China.
Yameng ZhongDepartment of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, 88 Jiaotong Road, Fuzhou, 350004, Fujian, China.
Min ChenDepartment of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, 88 Jiaotong Road, Fuzhou, 350004, Fujian, China. cmjy503@163.com.
Fujian Medical University · CNFujian Women and Children Hospital · CNFuzhou University · CNXiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study was to investigate the effects of Resveratrol (RSV) in rats with dilated cardiomyopathy (DCM).

methodsPorcine cardiac myosin was used to set up rat model with DCM. RSV (10 mg/kg in RSV-L group and 50 mg/kg in RSV-H group) or vehicle was administered to rats with DCM once daily from the 28th day till the 90th day after the first immunization. Cardiac function of rats was evaluated by echocardiographic analysis. The deposition of fibrous tissues in the hearts was evaluated by Masson and picrosirius red staining. The mRNA levels of collagen type I (Col I), collagen type III (Col III) and silence information regulator 1 (Sirt1) were measured by quantitative real-time polymerase chain reaction (qRT-PCR). The interaction of Sirt1 with Smad3 was revealed by coimmunoprecipitation.

resultsThe heart weight, heart weight/body weight ratio, left ventricular end diastolic diameter (LVEDD) and left ventricular end systolic diameter (LVESD) were significantly increased in rats with DCM, and attenuated by RSV. RSV also positively decreased fibrosis, and the expression of Col I and Col III in the myocardium. The Sirt1 mRNA was significantly decreased in myosin-immunized hearts and was positively increased by RSV. The Sirt1 combined with Smad3 directly. Acetylation of Smad3 (Ac-Smad3) was significantly increased in DCM and was markedly decreased by RSV.

conclusionRSV effectively ameliorated myocardial fibrosis and improved cardiac function by regulating Sirt1/Smad3 deacetylation pathway in rat model with DCM.

Indexed as

Gene Expression RegulationAnimalsBiopsyCardiomyopathy, DilatedDisease Models, AnimalEchocardiographyEnzyme InhibitorsFibrosisMaleMyocardiumResveratrolRNASirtuin 1Smad3 ProteinSwineEnzyme InhibitorsResveratrolRNASirt1 protein, ratSirtuin 1Smad3 ProteinDilated cardiomyopathyFibrosisResveratrolSirt1Smad3

Identifiers

PMID35081907
PMCPMC8793224
OpenAlexW4210614885

What OpenQuestion holds

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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.