Evidence map›Paper›PMID 19322943›Full record

ArticleAnesthesiology2009

Involvement of erythropoietin in retinal ischemic preconditioning.

John C Dreixler, Sarah Hagevik, Jonathan W Hemmert, Afzhal R Shaikh, Daniel M Rosenbaum, Steven Roth

Open access · bronzeAbstract read
In one paragraph

Article in Anesthesiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  12. Inhibition of histone deacetylase protects the retina from ischemic injury.Investigative ophthalmology & visual science · 2010
    Article
  13. Novel neuroprotective strategies in ischemic retinal lesions.International journal of molecular sciences · 2010
    Review
  14. Review
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  16. Article
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 4 institutions in 1 country.

John C DreixlerAnesthesia and Critical Care, University of Chicago, Chicago, Illinois 60637, USA.
Sarah Hagevik
Jonathan W Hemmert
Afzhal R Shaikh
Daniel M Rosenbaum
Steven Roth
University of Chicago Medical Center · USUniversity of Illinois Chicago · USSUNY Downstate Health Sciences University · USUniversity of Chicago · US

Funding

The Role of Adenosine in Retinal IschemiaR01EY010343 · NEI · UNIVERSITY OF CHICAGO · PI ROTH, STEVEN · 1994 to 2014
$4.8M
MECHANISM OF RETINAL ISCHEMIAR01EY011253 · NEI · YESHIVA UNIVERSITY · PI ROSENBAUM, DANIEL M. · 1997 to 2005
$1.8M
NEI NIH HHS EY10343NEI NIH HHS EY11253NEI NIH HHS R01 EY010343NEI NIH HHS R01 EY011253
6 · The paper itself

Abstract

backgroundThe purpose of this study was to examine the role of erythropoietin in retinal ischemic preconditioning (IPC).

methodsRats were subjected to retinal ischemia after IPC. Electroretinography assessed functional recovery after ischemia; retinal sections were examined to determine loss of retinal ganglion cells, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling was used to assess apoptosis. Levels of downstream mediators were measured in retinal homogenates by Western blotting. To assess the involvement of erythropoietin in IPC, Western blotting was used to measure levels of erythropoietin and its receptor (EPO-R) in retinal homogenates after IPC. To examine erythropoietin's role in IPC, the impact of blocking erythropoietin via intravitreal injection of soluble EPO-R (sEPO-R) before IPC was studied.

resultsErythropoietin levels did not change after IPC, but EPO-R increased. Intravitreal injection of sEPO-R significantly attenuated both the functional and histologic neuroprotection produced by IPC in comparison to control injection of denatured sEPO-R. Apoptotic damage after ischemia was enhanced in the sEPO-R-treated retinas as indicated by fluorescent terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling. Phosphorylated extracellular-signal-regulated kinase and heat shock protein 27, but not protein kinase B, upregulated in denatured sEPO-R-treated retinae, were attenuated in eyes injected with sEPO-R.

conclusionsThese results indicate that EPO-R upregulation is a critical component of the functional, histologic, and antiapoptotic protective effect of IPC on ischemia in the retina and that several downstream effectors may be involved in the neuroprotective actions of erythropoietin.

Indexed as

Ischemic PreconditioningRetinal VesselsAnimalsApoptosisBlotting, WesternDNA NucleotidylexotransferaseElectroretinographyErythropoietinExtracellular Signal-Regulated MAP KinasesFluorescent Antibody Technique, IndirectHSP27 Heat-Shock ProteinsIn Situ Nick-End LabelingNeuronsProto-Oncogene Proteins c-aktRatsRats, Sprague-DawleyDNA NucleotidylexotransferaseErythropoietinExtracellular Signal-Regulated MAP KinasesHSP27 Heat-Shock ProteinsProto-Oncogene Proteins c-aktReceptors, Erythropoietin

Identifiers

PMID19322943
PMCPMC2891304
OpenAlexW2091554988

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.