Evidence map›Paper›PMID 35124772›Full record

ArticleCell stress & chaperones2021

Activation of NRF2/FPN1 pathway attenuates myocardial ischemia-reperfusion injury in diabetic rats by regulating iron homeostasis and ferroptosis.

Hao Tian, Yonghong Xiong, Yi Zhang, Yan Leng, Jie Tao, Lu Li, Zhen Qiu, Zhongyuan Xia

Open access · hybridAbstract read
In one paragraph

Article in Cell stress & chaperones, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 2 pooled it
19.3field-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

96 citing papers in PubMed, 2 syntheses or guidelines pooled it, 135 citations in OpenAlex.

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  18. Polysaccharides Extraction fromFoods (Basel, Switzerland) · 2026
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36 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

8 authors at 2 institutions in 1 country.

Hao TianDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan, 430060, China.
Yonghong XiongDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan, 430060, China.
Yi ZhangDepartment of Anesthesiology and Perioperative Medicine, Shandong Qianfoshan Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Yan LengDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan, 430060, China.
Jie TaoDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan, 430060, China.
Lu LiDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan, 430060, China.
Zhen QiuDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan, 430060, China. qiuzhen124@126.com.
Zhongyuan XiaDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan, 430060, China. xiazhongyuan2005@aliyun.com.ORCID 0000-0002-5807-9554
Wuhan University · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In patients with ischemic heart disease, myocardial ischemia-reperfusion injury (IRI) can aggravate their condition even worse, and diabetes increases their risk of myocardial IRI. Pathological pathways of common diseases and surgical operations like diabetes, obesity, coronary artery angioplasty, and heart transplantation entail disorders of iron metabolism. Ferroportin1 (FPN1) is the only mammalian protein associated with iron release and thus plays a vital role in iron homeostasis, while nuclear factor E2-related factor 2 (NRF2) controls the transcription of FPN1. Since the NRF2/FPN1 pathway may play a favorable role in the therapy of diabetic myocardial IRI, this work investigated the possible mechanism. In this study, we investigated the effects of ferroptosis in STZ-induced diabetic rats following myocardial IRI in vivo, and its alteration in glucose and hypoxia/reoxygenation-induced cardiomyocytes injury in vitro. Rats and H9c2 cardiomyocytes were randomly divided into 6 groups and treated with sulforaphane and erastin besides the establishment of diabetic myocardial IRI and hyperglycemic hypoxia-reoxygenation models. Cardiac functional and structural damage were detected by Evans blue/TTC double staining, echocardiography, HE staining, and serological indices. CCK-8 assay and ROS production were used to measure cardiomyocyte viability and oxidative stress level. Additionally, the changes in cell supernatant levels of Fe

Indexed as

Diabetes Mellitus, ExperimentalFerroptosisMyocardial Reperfusion InjuryAnimalsHomeostasisHumansIronMammalsMyocytes, CardiacNF-E2-Related Factor 2RatsIronNF-E2-Related Factor 2DiabetesFerroptosisFPN1Iron homeostasisMyocardial ischemia–reperfusion injuryNRF2

Identifiers

PMID35124772
PMCPMC8943074
OpenAlexW4226343445

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.