Evidence map›Paper›PMID 33013403›Full record

ArticleFrontiers in pharmacology2020

Irisin Attenuates Myocardial Ischemia/Reperfusion Injury and Improves Mitochondrial Function Through AMPK Pathway in Diabetic Mice.

Chao Xin, Zheng Zhang, Guojie Gao, Liping Ding, Chao Yang, Chengzhu Wang, Yanjun Liu, Yufei Guo, Xueqing Yang, Lijuan Zhang and 4 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

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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

14 authors.

Chao XinDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Zheng ZhangDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Guojie GaoDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Liping DingDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Chao YangDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Chengzhu WangDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Yanjun LiuDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Yufei GuoDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Xueqing YangDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Lijuan ZhangDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Lina ZhangDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Yi LiuDepartment of Cardiology, Xijing Hospital, Air Force Medical University, Xi'an, China.
Zhitao JinDepartment of Cardiology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Ling TaoDepartment of Cardiology, Xijing Hospital, Air Force Medical University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsSeveral recent reports have shown irisin protects the heart against ischemia/reperfusion injury. However, the effect of irisin on I/R injury in diabetic mice has not been described. The present study was designed to investigate the role of irisin in myocardial ischemia-reperfusion (MI/R) injury in diabetic mice.

methodsA mouse model of diabetes was established by feeding wild type or gene-manipulated adult male mice with a high-fat diet. All the mice received intraperitoneal injection of irisin or PBS. Thirty minutes after injection, mice were subjected to 30 min of myocardial ischemia followed by 3h (for cell apoptosis and protein determination), 24 h (for infarct size and cardiac function).

resultsKnock-out of gene FNDC5 augmented MI/R injury in diabetic mice, while irisin treatment attenuated MI/R injury, improved cardiac function, cellular ATP biogenetics, mitochondria potential, and impaired mitochondrion-related cell death. More severely impaired AMPK pathway was observed in diabetic FNDC5

conclusionsOur present study demonstrated that irisin improves the mitochondria function and attenuates MI/R injury in diabetic mice through AMPK pathway.

Indexed as

AMPKdiabetesirisinischemia/reperfusionmitochondria

Identifiers

PMID33013403
PMCPMC7516196

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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.