Evidence map›Paper›PMID 25617620›Full record

ArticlePloS one2015

Role of neuronal NADPH oxidase 1 in the peri-infarct regions after stroke.

Dong-Hee Choi, Ji-Hye Kim, Kyoung-Hee Lee, Hahn-Young Kim, Yoon-Seong Kim, Wahn Soo Choi, Jongmin Lee

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Lentivirus- or AAV-mediated gene therapy interventions in ischemic stroke: A systematic review of preclinicalJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Pooled it
  2. Review
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  8. Role of NADPH Oxidases in Stroke Recovery.Antioxidants (Basel, Switzerland) · 2024
    Review
  9. NADPH Oxidase 3: Beyond the Inner Ear.Antioxidants (Basel, Switzerland) · 2024
    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 2 institutions in 2 countries.

Dong-Hee ChoiDepartment of Medical Science, Konkuk University School of Medicine, Seoul, Republic of Korea; Center for Neuroscience Research, Institute of Biomedical Science and Technology, Konkuk University, Seoul, Korea.
Ji-Hye KimCenter for Neuroscience Research, Institute of Biomedical Science and Technology, Konkuk University, Seoul, Korea.
Kyoung-Hee LeeCenter for Neuroscience Research, Institute of Biomedical Science and Technology, Konkuk University, Seoul, Korea.
Hahn-Young KimCenter for Neuroscience Research, Institute of Biomedical Science and Technology, Konkuk University, Seoul, Korea.
Yoon-Seong KimBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL 32827, United States of America.
Wahn Soo ChoiDepartment of Immunology and Physiology, Functional Genomics Institute, College of Medicine, Konkuk University, Chungju, Korea.
Jongmin LeeDepartment of Rehabilitation Medicine, Konkuk University School of Medicine, Seoul, Korea; Center for Neuroscience Research, Institute of Biomedical Science and Technology, Konkuk University, Seoul, Korea.
Konkuk University · KRUniversity of Central Florida · US

Funding

Role of NADPH oxidase 1-derived ROS in the pathogenesis of Parkinson's diseaseR01NS062827 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI KIM, YOON-SEONG · 2009 to 2012
$1.2M
NINDS NIH HHS R01 NS062827
6 · The paper itself

Abstract

The molecular mechanism underlying the selective vulnerability of neurons to oxidative damage caused by ischemia-reperfusion (I/R) injury remains unknown. We sought to determine the role of NADPH oxidase 1 (Nox1) in cerebral I/R-induced brain injury and survival of newborn cells in the ischemic injured region. Male Wistar rats were subjected to 90 min middle cerebral artery occlusion (MCAO) followed by reperfusion. After reperfusion, infarction size, level of superoxide and 8-hydroxy-2'-deoxyguanosine (8-oxo-2dG), and Nox1 immunoreactivity were determined. RNAi-mediated knockdown of Nox1 was used to investigate the role of Nox1 in I/R-induced oxidative damage, neuronal death, motor function recovery, and ischemic neurogenesis. After I/R, Nox1 expression and 8-oxo-2dG immunoreactivity was increased in cortical neurons of the peri-infarct regions. Both infarction size and neuronal death in I/R injury were significantly reduced by adeno-associated virus (AAV)-mediated transduction of Nox1 short hairpin RNA (shRNA). AAV-mediated Nox1 knockdown enhanced functional recovery after MCAO. The level of survival and differentiation of newborn cells in the peri-infarct regions were increased by Nox1 inhibition. Our data suggest that Nox-1 may be responsible for oxidative damage to DNA, subsequent cortical neuronal degeneration, functional recovery, and regulation of ischemic neurogenesis in the peri-infarct regions after stroke.

Indexed as

AnimalsAstrocytesBase SequenceBrainCell DeathCell DifferentiationCell SurvivalDependovirusDNAGene Expression Regulation, EnzymologicGene Knockdown TechniquesInfarction, Middle Cerebral ArteryMaleNADH, NADPH OxidoreductasesNADPH Oxidase 1Neural Stem CellsDNANADH, NADPH OxidoreductasesNADPH Oxidase 1NOX1 protein, ratSuperoxides

Identifiers

PMID25617620
PMCPMC4305324
OpenAlexW2023410769

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.