Evidence map›Paper›PMID 29979350›Full record

ArticleJournal of cardiovascular pharmacology2018

Irisin Protects Heart Against Ischemia-Reperfusion Injury Through a SOD2-Dependent Mitochondria Mechanism.

Zhen Wang, Ken Chen, Yu Han, Hua Zhu, Xinyu Zhou, Tao Tan, Jing Zeng, Jun Zhang, Yukai Liu, Yu Li and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of cardiovascular pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
7.1field-weighted citation impact, top 2% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 124 citations in OpenAlex.

  1. Pooled it
  2. Myokines and mitochondrial function in cardiometabolic diseases.Journal of physiology and biochemistry · 2026
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11 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

16 authors at 3 institutions in 2 countries.

Zhen WangDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Ken ChenDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Yu HanDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Hua ZhuDepartment of Surgery, Davis Heart and Lung Research Institute, Ohio State University, Columbus, OH.
Xinyu ZhouDepartment of Surgery, Davis Heart and Lung Research Institute, Ohio State University, Columbus, OH.
Tao TanDepartment of Surgery, Davis Heart and Lung Research Institute, Ohio State University, Columbus, OH.
Jing ZengDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Jun ZhangDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Yukai LiuDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Yu LiDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Yonggang YaoDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Jianxun YiDepartment of Physiology, Kansas City University of Medicine and Bioscience, Kansas City, MO.
Duofen HeDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Jingsong ZhouDepartment of Physiology, Kansas City University of Medicine and Bioscience, Kansas City, MO.
Jianjie MaDepartment of Surgery, Davis Heart and Lung Research Institute, Ohio State University, Columbus, OH.
Chunyu ZengDepartment of Cardiology, Daping Hospital, Third Military Medical University, Chongqing Institute of Cardiology, Chongqing, People's Republic of China.
Army Medical University · CNLung Institute · USDaping Hospital · CN

Funding

Targeting cell membrane repair for treatment of acute kidney injuryR01DK106394 · NIDDK · OHIO STATE UNIVERSITY · PI LIN, PEI-HUI, ROVIN, BRAD H · 2016 to 2020
$2.5M
Myokine function of MG53 in muscle injury-repair and regenerationR01AR070752 · NIAMS · OHIO STATE UNIVERSITY · PI HAN, RENZHI · 2017 to 2021
$1.7M
NIAMS NIH HHS R01 AR070752NIDDK NIH HHS R01 DK106394
6 · The paper itself

Abstract

Irisin, a muscle-origin protein derived from the extracellular domain of the fibronectin domain-containing 5 protein (FNDC5), has been shown to modulate mitochondria welfare through paracrine action. Here, we test the hypothesis that irisin contributes to cardioprotection after myocardial infarction by preserving mitochondrial function in cardiomyocytes. Animal model studies show that intravenous administration of exogenous irisin produces dose-dependent protection against ischemia/reperfusion (I/R)-induced injury to the heart as reflected by the improvement of left ventricular ejection fraction and the reduction in serum level of cTnI (n = 15, P < 0.05). I/R-induced apoptosis of cardiomyocytes is reduced after irisin treatment. The irisin-mediated protection has, at least in part, an effect on mitochondrial function because administration of irisin increases irisin staining in the mitochondria of the infarct area. Irisin also reduces I/R-induced oxidative stress as determined by mitochondrial membrane potential evaluation and superoxide FLASH event recording (n = 4, P < 0.05). The interaction between irisin and superoxide dismutase2 (SOD2) plays a key role in the protective process because irisin treatment increases SOD activity (n = 10, P < 0.05) and restores the mitochondria localization of SOD2 in cardiomyocytes (n = 5, P < 0.05). These results demonstrate that irisin plays a protective role against I/R injury to the heart. Targeting the action of irisin in mitochondria presents a novel therapeutic intervention for myocardial infarction.

Indexed as

AnimalsAntioxidantsApoptosisCell LineDisease Models, AnimalFibronectinsMembrane Potential, MitochondrialMitochondria, HeartMyocardial InfarctionMyocardial Reperfusion InjuryMyocytes, CardiacOxidative StressRats, Sprague-DawleySignal TransductionStroke VolumeSuperoxide DismutaseAntioxidantsFibronectinsSuperoxide DismutaseSuperoxide Dismutase 2Troponin I

Identifiers

PMID29979350
PMCPMC6283696
OpenAlexW2810889974

What OpenQuestion holds

Textmetadata
LicenceTDM
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.