Evidence map›Paper›PMID 35676606›Full record

ArticleInflammation2022

Dapagliflozin Alleviates Coxsackievirus B3-induced Acute Viral Myocarditis by Regulating the Macrophage Polarization Through Stat3-related Pathways.

Pengcheng Yan, Xiaoning Song, Joanne Tran, Runfa Zhou, Xinran Cao, Gang Zhao, Haitao Yuan

Open access · hybridAbstract read
In one paragraph

Article in Inflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Anti-Inflammatory Effects of SGLT2 Inhibitors: Focus on Macrophages.International journal of molecular sciences · 2025
    Review
  6. Review
  7. Article
  8. Review
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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

7 authors at 3 institutions in 2 countries.

Pengcheng YanDepartment of Cardiology, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, 250021, People's Republic of China.
Xiaoning SongDepartment of Cardiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250021, People's Republic of China.
Joanne TranUniversity of Portland, Portland, Oregon, 97239, USA.
Runfa ZhouDepartment of Cardiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250021, People's Republic of China.
Xinran CaoDepartment of Cardiology, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, 250021, People's Republic of China.
Gang ZhaoDepartment of Cardiology, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, 250021, People's Republic of China. zg000507@163.com.ORCID http://orcid.org/0000-0002-9939-9001
Haitao YuanDepartment of Cardiology, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, 250021, People's Republic of China. doctoryuanht@126.com.
Shandong Provincial Hospital · CNShandong University · CNUniversity of Portland · US

Funding

Health and Family Planning Commission of Shandong Province 2018WS272Human Resources and Social Security department of Shandong province 201903087Jinan Science and Technology Bureau 201907033Key Technology Research and Development Program of Shandong 2018GSF118109National Natural Science Foundation of China 81770382Natural Science Foundation of Shandong Province ZR2020MH031
6 · The paper itself

Abstract

Viral myocarditis (VMC), which is most prevalently caused by Coxsackievirus B3 (CVB3) infection, is a serious clinical condition characterized by cardiac inflammation. Dapagliflozin, a kind of sodium glucose co-transporters 2(SGLT-2) inhibitor, exhibited protective effects on plenty of inflammatory diseases, while its effect on viral myocarditis has not been studied. Recently, we found the protective effect of dapagliflozin on VMC. After CVB3 infection, dapagliflozin and STATTIC (a kind of stat3 inhibitor) were given to Balb/c male mice for 8 days, and then the severity of myocarditis was assessed. Our results indicated that dapagliflozin significantly alleviated the severity of viral myocarditis, elevated the survival rate, and ameliorated cardiac function. Besides, dapagliflozin can decrease the level of pro-inflammatory cytokines including IL-1β, IL-6, and TNF-α. Furthermore, dapagliflozin can inhibit macrophages differentiate to classically activated macrophages (M1) in cardiac tissue and activate the Stat3 signal pathway which is reported to promote polarization of the alternatively activated macrophage (M2). And STATTIC can reverse these changes caused by dapagliflozin. In conclusion, we found that dapagliflozin treatment increased anti-inflammatory macrophage polarization and reduced cardiac injury following VMC via activating Stat3 signal pathway.

Indexed as

Coxsackievirus InfectionsMyocarditisSymportersAnimalsBenzhydryl CompoundsCyclic S-OxidesCytokinesEnterovirus B, HumanGlucoseGlucosidesInterleukin-6MacrophagesMaleMiceMice, Inbred BALB CSodiumBenzhydryl CompoundsCyclic S-OxidesCytokinesdapagliflozinGlucoseGlucosidesInterleukin-6SodiumstatticSymportersTumor Necrosis Factor-alphadapagliflozinmacrophage polarizationStat3viral myocarditis

Identifiers

PMID35676606
PMCPMC9499897
OpenAlexW4282941033

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.