Evidence map›Paper›PMID 32286488›Full record

ArticleScientific reports2020

Up-regulation of pro-angiogenic pathways and induction of neovascularization by an acute retinal light damage.

A Tisi, G Parete, V Flati, R Maccarone

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

A Tisi *Department of Biotechnology and Applied Clinical Sciences, University of L'Aquila, via Vetoio, Coppito 2, 67100, L'Aquila, Italy.
G Parete *Department of Biotechnology and Applied Clinical Sciences, University of L'Aquila, via Vetoio, Coppito 2, 67100, L'Aquila, Italy.
V FlatiDepartment of Biotechnology and Applied Clinical Sciences, University of L'Aquila, via Vetoio, Coppito 2, 67100, L'Aquila, Italy.ORCID http://orcid.org/0000-0003-1014-297X
R MaccaroneDepartment of Biotechnology and Applied Clinical Sciences, University of L'Aquila, via Vetoio, Coppito 2, 67100, L'Aquila, Italy. rita.maccarone@univaq.it.
University of L'Aquila · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The light damage (LD) model was mainly used to study some of the main aspects of age related macular degeneration (AMD), such as oxidative stress and photoreceptor death. Several protocols of light-induced retinal degeneration exist. Acute light damage is characterized by a brief exposure (24 hours) to high intensity light (1000 lux) and leads to focal degeneration of the retina which progresses over time. To date there are not experimental data that relate this model to neovascular events. Therefore, the purpose of this study was to characterize the retina after an acute light damage to assess whether the vascularization was affected. Functional, molecular and morphological investigations were carried out. The electroretinographic response was assessed at all recovery times (7, 60, 120 days after LD). Starting from 7 days after light damage there was a significant decrease in the functional response, which remained low up to 120 days of recovery. At 7 days after light exposure, neo-vessels invaded the photoreceptor layer and retinal neovascularization occurred. Remarkably, neoangiogenesis was associated to the up-regulation of VEGF, bFGF and their respective receptors (VEGFR2 and FGFR1) with the progression of degeneration. These important results indicate that a brief exposure to bright light induces the up-regulation of pro-angiogenic pathways with subsequent neovascularization.

Indexed as

RetinaAnimalsMacular DegenerationNeovascularization, PathologicPhotoreceptor Cells, VertebrateRadiation Injuries, ExperimentalRats, Sprague-DawleyUp-RegulationVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID32286488
PMCPMC7156521
OpenAlexW3016235323

What OpenQuestion holds

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LicenceCC BY
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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.