Evidence map›Paper›PMID 22282883›Full record

ArticleStroke2012

Pyruvate protects the brain against ischemia-reperfusion injury by activating the erythropoietin signaling pathway.

Myoung-Gwi Ryou, Ran Liu, Ming Ren, Jie Sun, Robert T Mallet, Shao-Hua Yang

Open access · bronzeAbstract read
In one paragraph

Article in Stroke, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 87 citations in OpenAlex.

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  12. The mitochondrial pyruvate carrier at the crossroads of intermediary metabolism.American journal of physiology. Endocrinology and metabolism · 2022
    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

6 authors at 1 institution in 1 country.

Myoung-Gwi RyouDepartment of Pharmacology and Neuroscience, University of North Texas Health Science Center, 3500 Camp Bowie Boulevard, Fort Worth, TX 76107-2699, USA.
Ran Liu
Ming Ren
Jie Sun
Robert T Mallet
Shao-Hua Yang
University of North Texas · US

Funding

Training in the Neurobiology of Aging and Alzheimer's DiseaseT32AG020494 · NIA · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI ROBERT Clinton BARBER, NATHALIE SUMIEN · 2002 to 2026
$6.9M
Vascular Cognitive Impairment Induced by Ischemic Stroke: mechanism and therapyR01NS054651 · NINDS · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI YANG, SHAOHUA · 2008 to 2012
$1.6M
Pyruvate: Powerful Brain Protection after Cardiac ArrestR01NS076975 · NINDS · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI MALLET, ROBERT T · 2011 to 2014
$1.4M
Interaction of Estrogen and Tissue Plasminogen ActivatorR01NS054687 · NINDS · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI YANG, SHAOHUA · 2008 to 2011
$1.0M
NIA NIH HHS AG020494NIA NIH HHS T32 AG020494NINDS NIH HHS NS054651NINDS NIH HHS NS054687NINDS NIH HHS NS076975NINDS NIH HHS R01 NS054651NINDS NIH HHS R01 NS054687NINDS NIH HHS R01 NS076975
6 · The paper itself

Abstract

background and purposePyruvate is known to be cytoprotective through antioxidant and anti-inflammatory mechanisms. We tested the hypothesis that pyruvate protects the brain against ischemia-reperfusion injury by inducing endogenous erythropoietin (EPO) expression.

methodsPyruvate's protective effect was evaluated in C6 glioma cells and HT22 neuronal cells subjected to transient oxygen glucose deprivation. Cell viability (calcein AM assay) and expression of hypoxia-inducible factor-1α, EPO, Akt and Erk (immunoblot), and EPO receptor (reverse transcription-polymerase chain reaction) were analyzed. Transient focal cerebral ischemia in rats was induced by 2 hours middle cerebral artery occlusion followed by 24 hours reperfusion. Pyruvate or saline was infused from 60 minutes occlusion until 30 minutes reperfusion. Lesion volume and DNA fragmentation were assessed by 2,3,5-triphenyltetrazolium staining and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling assay, respectively. Immunoblots were conducted to determine cerebral EPO contents.

resultsPyruvate increased cell viability, hypoxia-inducible factor-1α, EPO, and Akt phosphorylation. Small interfering RNA suppression of hypoxia-inducible factor-1α and EPO abolished pyruvate-induced cytoprotection. In the rat stroke model, pyruvate reduced lesion volume by 84% and DNA fragmentation by 77% versus controls; increased EPO content paralleled these cerebroprotective actions of pyruvate.

conclusionsPyruvate activation of the hypoxia-inducible factor-1α-EPO signaling cascade in neurons and glia could protect the brain from ischemia-reperfusion injury.

Indexed as

AnimalsBrainCell Line, TumorDisease Models, AnimalErythropoietinGene Expression RegulationHypoxia-Inducible Factor 1, alpha SubunitMaleMiceProto-Oncogene Proteins c-aktPyruvic AcidRatsRats, Sprague-DawleyReceptors, ErythropoietinReperfusion InjurySignal TransductionErythropoietinHif1a protein, mouseHif1a protein, ratHypoxia-Inducible Factor 1, alpha SubunitProto-Oncogene Proteins c-aktPyruvic AcidReceptors, Erythropoietin

Identifiers

PMID22282883
PMCPMC3314723
OpenAlexW2137499753

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.