Evidence map›Paper›PMID 26750922›Full record

ArticleBMC cardiovascular disorders2016

Resveratrol ameliorates myocardial fibrosis by inhibiting ROS/ERK/TGF-β/periostin pathway in STZ-induced diabetic mice.

Han Wu, Guan-Nan Li, Jun Xie, Ran Li, Qin-Hua Chen, Jian-Zhou Chen, Zhong-Hai Wei, Li-Na Kang, Biao Xu

Open access · goldAbstract read
In one paragraph

Article in BMC cardiovascular disorders, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
11.9field-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

62 citing papers in PubMed, 117 citations in OpenAlex.

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2 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

9 authors at 1 institution in 1 country.

Han WuDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.
Guan-Nan LiDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.
Jun XieDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.
Ran LiDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.
Qin-Hua ChenDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.
Jian-Zhou ChenDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.
Zhong-Hai WeiDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.
Li-Na KangDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China. army0001@163.com.
Biao XuDepartment of Cardiology, Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China. xubiao@medmail.com.cn.
Nanjing Drum Tower Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyocardial fibrosis is an essential hallmark of diabetic cardiomyopathy (DCM) contributing to cardiac dysfunctions. Resveratrol, an antioxidant, exerts its anti-fibrotic effect via inhibition of oxidative stress, while the underlying molecular mechanism remains largely elusive. Periostin, a fibrogenesis matricellular protein, has been shown to be associated with oxidative stress. In the present study, we investigated the role of periostin in anti-fibrotic effect of resveratrol in streptozocin (STZ)-induced diabetic heart and the underlying mechanisms.

methodsDiabetic mice were induced by STZ injection. After treatment with resveratrol (5 or 25 mg/kg/day i.g) or Saline containing 0.5% carboxymethyl cellulose (CMC) for 2 months, the hearts were detected for oxidative stress and cardiac fibrosis using western blot, Masson's trichrome staining and Dihydroethidium (DHE) staining. In in vitro experiments, proliferation and differentiation of fibroblasts under different conditions were investigated through western blot, 3-(4,5)-dimethylthiahiazo (-z-y1)-3,5-di-phenytetrazoliumromide (MTT) assay and immunofluorescence staining.

resultsAdministration of resveratrol significantly mitigated oxidative level, interstitial fibrosis and expressions of related proteins in STZ-induced diabetic hearts. In in vitro experiments, resveratrol exhibited anti-proliferative effect on primary mouse cardiac fibroblasts via inhibiting reactive oxygen species (ROS)/extracellular regulated kinase (ERK) pathway and ameliorated myofibroblast differentiation via suppressing ROS/ERK/ transforming growth factor β (TGF-β)/periostin pathway.

conclusionIncreased ROS production, activation of ERK/TGF-β/periostin pathway and myocardial fibrosis are important events in DCM. Alleviated ROS genesis by resveratrol prevents myocardial fibrosis by regulating periostin related signaling pathway. Thus, inhibition of ROS/periostin may represent a novel approach for resveratrol to reverse fibrosis in DCM.

Indexed as

AnimalsAntioxidantsCell Adhesion MoleculesDiabetes Mellitus, ExperimentalDiabetic CardiomyopathiesFibrosisHeartMaleMAP Kinase Signaling SystemMiceMyocardiumOxidative StressReactive Oxygen SpeciesResveratrolSignal TransductionStilbenesAntioxidantsCell Adhesion MoleculesPostn protein, mouseReactive Oxygen SpeciesResveratrolStilbenesTransforming Growth Factor beta

Identifiers

PMID26750922
PMCPMC4707778
OpenAlexW2224692388

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.