Evidence map›Paper›PMID 26239818›Full record

ArticleNeuropharmacology2015

Retinal ganglion cell neuroprotection induced by activation of alpha7 nicotinic acetylcholine receptors.

David Mata, David M Linn, Cindy L Linn

Abstract read
In one paragraph

Article in Neuropharmacology, 2015. 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
1.7field-weighted citation impact, top 17% 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, 31 citations in OpenAlex.

  1. Article
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  6. BrdU Positive Cells Induced in a Genetic Mouse Model of Glaucoma.Journal of ophthalmology & visual sciences · 2021
    Article
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  8. Involvement ofFrontiers in molecular biosciences · 2020
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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

3 authors at 2 institutions in 1 country.

David MataWestern Michigan University, Department of Biological Sciences, Kalamazoo, MI 49008, USA. Electronic address: David_Mata@rush.edu.
David M LinnGrand Valley State University, Department of Biomedical Sciences, Allendale, MI 49401, USA. Electronic address: linnd@gvsu.edu.
Cindy L LinnWestern Michigan University, Department of Biological Sciences, Kalamazoo, MI 49008, USA. Electronic address: cindy.linn@wmich.edu.
Western Michigan University · USGrand Valley State University · US

Funding

Prevention of RGC loss in an in vitro excitotoxic model and an in vivo model of gR15EY022795 · NEI · WESTERN MICHIGAN UNIVERSITY · PI LINN, CINDY L · 2012 to 2012
$416k
NEI NIH HHS EY 022795NEI NIH HHS R15 EY022795
6 · The paper itself

Abstract

The α7nAChR agonist, PNU-282987, has previously been shown to have a neuroprotective effect against loss of retinal ganglion cells (RGCs) in an in vivo glaucoma model when the agent was injected into the vitreous chamber of adult Long Evans rat eyes. Here, we characterized the neuroprotective effect of PNU-282987 at the nerve fiber and retinal ganglion cell layer, determined that neuroprotection occurred when the agonist was applied as eye drops and verified detection of the agonist in the retina, using LC/MS/MS. To induce glaucoma-like conditions in adult Long Evans rats, hypertonic saline was injected into the episcleral veins to induce scar tissue and increase intraocular pressure. Within one month, this procedure produced significant loss of RGCs compared to untreated conditions. RGCs were quantified after immunostaining with an antibody against Thy 1.1 and imaged using a confocal microscope. In dose-response studies, concentrations of PNU-282987 were applied to the animal's right eye two times each day, while the left eye acted as an internal control. Eye drops of PNU-282987 resulted in neuroprotection against RGC loss in a dose-dependent manner using concentrations between 100 μM and 2 mM PNU-282987. LC/MS/MS results demonstrated that PNU-282987 was detected in the retina when applied as eye drops, relatively small amounts of PNU-282987 were measured in blood plasma and no PNU-282987 was detected in cardiac tissue. These results support the hypothesis that eye drop application of PNU-282987 can prevent loss of RGCs associated with glaucoma, which can lead to neuroprotective treatments for diseases that involve α7nAChRs.

Indexed as

alpha7 Nicotinic Acetylcholine ReceptorAnimalsBenzamidesBridged Bicyclo CompoundsDisease Models, AnimalDose-Response Relationship, DrugDrug Evaluation, PreclinicalFemaleGlaucomaHeartMaleMicroscopy, ConfocalMyocardiumNeuroprotective AgentsOphthalmic SolutionsRats, Long-Evansalpha7 Nicotinic Acetylcholine ReceptorBenzamidesBridged Bicyclo CompoundsNeuroprotective AgentsOphthalmic SolutionsPNU-282987Saline Solution, HypertonicAcetylcholine receptorsAdult ratsGlaucomaNerve fiber layerNeuroprotectionRetinal ganglion cells

Identifiers

PMID26239818
PMCPMC4655168
OpenAlexW1009451482

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.