Evidence map›Paper›PMID 23702780›Full record

ArticleInvestigative ophthalmology & visual science2013

Neuroprotectin D1 restores corneal nerve integrity and function after damage from experimental surgery.

Maria Soledad Cortina, Jiucheng He, Tiffany Russ, Nicolas G Bazan, Haydee E P Bazan

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.5field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
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  7. Novel lipid mediator 7Frontiers in cell and developmental biology · 2024
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  11. Elucidating the structure and functions of Resolvin D6 isomers on nerve regeneration with a distinctive trigeminal transcriptome.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  12. Article
  13. Review
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  15. Mouse strains and sexual divergence in corneal innervation and nerve regeneration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
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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

5 authors at 2 institutions in 1 country.

Maria Soledad CortinaDepartment of Ophthalmology, University of Illinois Medical Center, Chicago, Illinois, USA.
Jiucheng He
Tiffany Russ
Nicolas G Bazan
Haydee E P Bazan
Louisiana State University Health Sciences Center New Orleans · USUniversity of Chicago Medical Center · US

Funding

Lipid Mediators in Corneal Nerve RegenerationR01EY019465 · NEI · LSU HEALTH SCIENCES CENTER · PI BAZAN, HAYDEE E.P. · 2009 to 2021
$4.0M
NEI NIH HHS R01 EY019465NEI NIH HHS R01EY019465
6 · The paper itself

Abstract

purposeTo investigate if topical treatment of neuroprotectin D1 (NPD1) increases regeneration of functional nerves after lamellar keratectomy.

methodsAn 8-mm stromal dissection was performed in the left eye of each rabbit. The rabbits were treated with NPD1, pigment epithelial-derived factor (PEDF) in combination with docosahexaenoic acid (DHA) or vehicle for 6 weeks, and corneas were obtained at 8 weeks. After fixation, corneal wholemounts were stained with mouse monoclonal anti-βIII-tubulin antibody and double stained with chicken anti-calcitonin gene-related peptide (CGRP) antibody. Corneal sensitivity and tear secretion were measured using the Cochet-Bonnet esthesiometer and the Schirmer's test, respectively. Additional rabbits were treated with NPD1, PEDF+DHA, or vehicle, and corneal sections were stained with a rat monoclonal anti-neutrophil antibody. Cultures of trigeminal ganglia from 5-day-old mice were treated with NPD1, PEDF+DHA, lipoxin A4 (LXA4), 12- or 15-hydroxyeicosatetraenoic acid (12[S] or 15[S]-HETE), and nerve growth factor (NGF) as positive control.

resultsNPD1 increased subepithelial corneal nerve area three times compared with vehicle-treated rabbits. The effect was similar to PEDF+DHA-treated animals. There was recovery of CGRP-positive neurons and an increase in corneal sensitivity and tear secretion in NPD1-treated animals. NPD1 decreased neutrophil infiltration after 2 and 4 days of treatment. In the in vitro cultures, NPD1 and PEDF+DHA induced a 3-fold increase in neurite outgrowth compared with cultures without supplementation. Treatments with LXA4, 12(S)-, and 15(S)- HETE did not stimulate neurite outgrowth.

conclusionsNPD1 has anti-inflammatory and nerve regenerative properties. This study demonstrates that NPD1 may offer an effective treatment for neurotrophic corneas.

Indexed as

AnimalsAxonsCalcitonin Gene-Related PeptideCells, CulturedCorneaDocosahexaenoic AcidsDrug CombinationsEye ProteinsFluorescent Antibody Technique, IndirectMiceNerve Growth FactorsNerve RegenerationNeuritesOphthalmic NervePigment Epithelium-Derived FactorRabbitsCalcitonin Gene-Related PeptideDocosahexaenoic AcidsDrug CombinationsEye ProteinsNerve Growth FactorsPigment Epithelium-Derived Factorprotectin D1SerpinsTubulincorneal sensitivitydry eyeneuroprotectin D1neuroregenerationpigment epithelial-derived factor

Identifiers

PMID23702780
PMCPMC3681478
OpenAlexW2001202192

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.