Evidence map›Paper›PMID 25210480›Full record

ArticleOphthalmology and eye diseases2014

Time-dependent Gene Profiling Indicates the Presence of Different Phases for Ischemia/Reperfusion Injury in Retina.

Kalina Andreeva, Meixia Zhang, Wei Fan, Xiaohong Li, Yinlu Chen, Jovan D Rebolledo-Mendez, Nigel G Cooper

Abstract read
In one paragraph

Article in Ophthalmology and eye diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Key immune regulators in retinal ischemia-reperfusion injuryInternational journal of ophthalmology · 2025
    Article
  3. Review
  4. Article
  5. Large-Scale Protein Analysis of Experimental Retinal Artery Occlusion.International journal of molecular sciences · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Treatment with ACell death & disease · 2017
    Article
  20. 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

7 authors.

Kalina AndreevaDepartment of Anatomical Sciences and Neurobiology, University of Louisville, School of Medicine, Louisville, KY, USA.
Meixia ZhangDepartment of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Wei FanDepartment of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Xiaohong LiDepartment of Anatomical Sciences and Neurobiology, University of Louisville, School of Medicine, Louisville, KY, USA.
Yinlu ChenDepartment of Anatomical Sciences and Neurobiology, University of Louisville, School of Medicine, Louisville, KY, USA.
Jovan D Rebolledo-MendezDepartment of Anatomical Sciences and Neurobiology, University of Louisville, School of Medicine, Louisville, KY, USA.
Nigel G CooperDepartment of Anatomical Sciences and Neurobiology, University of Louisville, School of Medicine, Louisville, KY, USA.

Funding

WKU Lead Faculty AwardP20GM103436 · NIGMS · UNIVERSITY OF LOUISVILLE · PI ERIC C ROUCHKA · 2012 to 2026
$60.1M
ZEBRAFISH VISUAL FUNCTION RECOVERY FOLLOWING OPTIC NERVE DAMAGEP20RR016481 · NCRR · UNIVERSITY OF LOUISVILLE · PI BARTON, HAZEL A · 2001 to 2011
$34.8M
The Role of CaMKII in Cell Death and Survival Responses of Retinal Ganglion CellsR01EY017594 · NEI · UNIVERSITY OF LOUISVILLE · PI COOPER, NIGEL G.F. · 2008 to 2011
$1.4M
NCRR NIH HHS P20 RR016481NEI NIH HHS R01 EY017594NIGMS NIH HHS P20 GM103436
6 · The paper itself

Abstract

Ischemia/reperfusion (IR) injury has been associated with several retinal pathologies, and a few genes/gene products have been linked to IR injury. However, the big picture of temporal changes, regarding the affected gene networks, pathways, and processes remains to be determined. The purpose of the present study was to investigate initial, intermediate, and later stages to characterize the etiology of IR injury in terms of the pathways affected over time. Analyses indicated that at the initial stage, 0-hour reperfusion following the ischemic period, the ischemia-associated genes were related to changes in metabolism. In contrast, at the 24-hour time point, the signature events in reperfusion injury include enhanced inflammatory and immune responses as well as cell death indicating that this would be a critical period for the development of any interventional therapeutic strategies. Genes in the signal transduction pathways, particularly transmitter receptors, are downregulated at this time. Activation of the complement system pathway clearly plays an important role in the later stages of reperfusion injury. Together, these results demonstrate that the etiology of injury related to IR is characterized by the appearance of specific patterns of gene expression at any given time point during retinal IR injury. These results indicate that evaluation of treatment strategies with respect to time is very critical.

Indexed as

gene expressionischemia/reperfusion (IR) injurymicroarrayretina

Identifiers

PMID25210480
PMCPMC4149383

What OpenQuestion holds

Textmetadata
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.