Evidence map›Paper›PMID 35280686›Full record

ArticleInternational journal of biological sciences2022

Keap-NRF2 signaling contributes to the Notch1 protected heart against ischemic reperfusion injury via regulating mitochondrial ROS generation and bioenergetics.

Hua Xu, Xiao-Dan Wan, Rong-Rong Zhu, Jin-Long Liu, Ji-Chun Liu, Xue-Liang Zhou

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
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

6 authors at 3 institutions in 1 country.

Hua XuDepartment of Cardiac Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, Jiangxi 330006, China.
Xiao-Dan WanDepartment of Electrocardiogram, The First Affiliated Hospital, Nanchang University, Nanchang, Jiangxi 330006, China.
Rong-Rong ZhuDepartment of Obstetrics and Gynecology, Gaoxin Hospital of the First Affiliated Hospital of Nanchang University, Nanchang, China.
Jin-Long LiuZhangjiang Institute, Fudan University, Shanghai, China.
Ji-Chun LiuDepartment of Cardiac Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, Jiangxi 330006, China.
Xue-Liang ZhouDepartment of Cardiac Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, Jiangxi 330006, China.
First Affiliated Hospital of Nanchang University · CNFudan University · CNNanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myocardial ischemia/reperfusion (I/R) injury is recognized as the leading cause of death worldwide. However, the molecular mechanisms involved in this process are still not fully understood. We previously reported that the combined action of Notch1 and Keap1-NRF2 signaling pathway can significantly increase the activity of cardiomyocytes, inhibit the apoptosis of cardiomyocytes, reduce the formation of reactive oxygen species, and improve the antioxidant activity in neonate rat myocardial cells. However, the regulatory mechanism of Notch1 signaling pathway on the NRF2 signaling pathway and its actual role on I/R injury are still unclear. Herein, we found that Keap-NRF2 signaling is activated by Notch1 in RBP-Jκ dependent manner, thus protects the heart against I/R injury via inhibiting the mitochondrial ROS generation and improves the mitochondrial bioenergetics in vitro and in vivo. These results suggest that Keap-NRF2 signaling might become a promising therapeutic strategy for treating myocardial I/R injury.

Indexed as

Myocardial Reperfusion InjuryReperfusion InjuryAnimalsApoptosisEnergy MetabolismKelch-Like ECH-Associated Protein 1Myocytes, CardiacNF-E2-Related Factor 2Oxidative StressRatsReactive Oxygen SpeciesReceptor, Notch1Signal TransductionKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2Notch1 protein, ratReactive Oxygen SpeciesReceptor, Notch1ischemic reperfusion injurymitochondrial bioenergeticsmitochondrial ROSNotch1NRF2

Identifiers

PMID35280686
PMCPMC8898363
OpenAlexW4210850668

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.