Evidence map›Paper›PMID 25722210›Full record

ArticleInvestigative ophthalmology & visual science2015

Progressive degeneration of retinal and superior collicular functions in mice with sustained ocular hypertension.

Hui Chen, Yan Zhao, Mingna Liu, Liang Feng, Zhen Puyang, Ji Yi, Peiji Liang, Hao F Zhang, Jianhua Cang, John B Troy and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
6.8field-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

62 citing papers in PubMed, 82 citations in OpenAlex.

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  20. Angiopoietin-1 Is Required for Vortex Vein and Choriocapillaris Development in Mice.Arteriosclerosis, thrombosis, and vascular biology · 2022
    Article

2 more citing papers are in PubMed but not listed here.

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

11 authors at 2 institutions in 2 countries.

Hui ChenDepartment of Ophthalmology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States.
Yan ZhaoDepartment of Biomedical Engineering, Robert R. McCormick School of Engineering and Applied Science, Northwestern University, Evanston, Illinois, United States.
Mingna LiuDepartment of Neurobiology, Weinberg College of Arts and Sciences, Northwestern University, Evanston, Illinois, United States.
Liang FengDepartment of Ophthalmology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States.
Zhen PuyangDepartment of Biomedical Engineering, Robert R. McCormick School of Engineering and Applied Science, Northwestern University, Evanston, Illinois, United States School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Ji YiDepartment of Biomedical Engineering, Robert R. McCormick School of Engineering and Applied Science, Northwestern University, Evanston, Illinois, United States.
Peiji LiangSchool of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Hao F ZhangDepartment of Ophthalmology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States Department of Biomedical Engineering, Robert R. McCormick School of Engineering and Applied Science, Northwestern University, Evanston, Illinois, United States.
Jianhua CangDepartment of Neurobiology, Weinberg College of Arts and Sciences, Northwestern University, Evanston, Illinois, United States.
John B TroyDepartment of Biomedical Engineering, Robert R. McCormick School of Engineering and Applied Science, Northwestern University, Evanston, Illinois, United States.
Xiaorong LiuDepartment of Ophthalmology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States Department of Neurobiology, Weinberg College of Arts and Sciences, Northwestern University, Evanston, Illinois, United States.
Northwestern University · USShanghai Jiao Tong University · CN

Funding

Novel Antiangiogenic Peptides for Treatment of Exudative AMDR24EY022883 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI SHEIBANI, NADER · 2013 to 2017
$6.2M
Neural Mechanisms of Stereoscopic VisionR01EY020950 · NEI · UNIVERSITY OF VIRGINIA · PI Jianhua Cang · 2010 to 2026
$5.9M
Multimodal Retinal Functional Imaging for Diabetic RetinopathyR01EY019951 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI FAWZI, AMANI A, JIAO, SHULIANG · 2011 to 2015
$3.0M
Neurotrophic Mechanisms in Retinal Ganglion Cell MaturationR01EY019034 · NEI · NORTHWESTERN UNIVERSITY · PI LIU, XIAORONG · 2008 to 2011
$1.4M
A nanoelectrode for neurophysiology &neuroprostheticsR21EB004200 · NIBIB · NORTHWESTERN UNIVERSITY · PI TROY, JOHN B · 2004 to 2005
$285k
NEI NIH HHS EY020950NEI NIH HHS R01 EY019034NEI NIH HHS R01EY019034NEI NIH HHS R01EY01995NEI NIH HHS R01 EY019951NEI NIH HHS R01 EY020950NEI NIH HHS R24 EY022883NIBIB NIH HHS R21 EB004200NIBIB NIH HHS R21EB004200
6 · The paper itself

Abstract

purposeWe investigated the progressive degeneration of retinal and superior collicular functions in a mouse model of sustained ocular hypertension.

methodsFocal laser illumination and injection of polystyrene microbeads were used to induce chronic ocular hypertension. Retinal ganglion cell (RGC) loss was characterized by in vivo optical coherence tomography (OCT) and immunohistochemistry. Retinal dysfunction was also monitored by the full-field ERG. Retinal ganglion cell light responses were recorded using a 256-channel multielectrode array (MEA), and RGC subtypes were characterized by noncentered spike-triggered covariance (STC-NC) analysis. Single-unit extracellular recordings from superficial layers of the superior colliculus (SC) were performed to examine the receptive field (RF) properties of SC neurons.

resultsThe elevation of intraocular pressure (IOP) lasted 4 months in mice treated with a combination of laser photocoagulation and microbead injection. Progressive RGC loss and functional degeneration were confirmed in ocular hypertensive (OHT) mice. These mice had fewer visually responsive RGCs than controls. Using the STC-NC analysis, we classified RGCs into ON, OFF, and ON-OFF functional subtypes. We showed that ON and OFF RGCs were more susceptible to the IOP elevation than ON-OFF RGCs. Furthermore, SC neurons of OHT mice had weakened responses to visual stimulation and exhibited mismatched ON and OFF subfields and irregular RF structure.

conclusionsWe demonstrated that the functional degeneration of RGCs is subtype-dependent and that the ON and OFF pathways from the retina to the SC were disrupted. Our study provides a foundation to investigate the mechanisms underlying the progressive vision loss in experimental glaucoma.

Indexed as

Action PotentialsAnimalsDisease Models, AnimalDisease ProgressionElectroretinographyFemaleGlaucomaMiceOcular HypertensionRetinaRetinal DegenerationRetinal Ganglion CellsSuperior ColliculiTomography, Optical Coherencemultielectrode arrayneural degenerationocular hypertensionretinal ganglion cellssuperior colliculus

Identifiers

PMID25722210
PMCPMC4365983
OpenAlexW2070165705

What OpenQuestion holds

Textmetadata
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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.