Evidence map›Paper›PMID 23986234›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Block of gap junctions eliminates aberrant activity and restores light responses during retinal degeneration.

Abduqodir H Toychiev, Elena Ivanova, Christopher W Yee, Botir T Sagdullaev

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

63 citing papers in PubMed, 87 citations in OpenAlex.

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  14. Impact of Retinal Degeneration on Response of ON and OFF Cone Bipolar Cells to Electrical Stimulation.IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society · 2023
    Article
  15. Article
  16. Implications of Neural Plasticity in Retinal Prosthesis.Investigative ophthalmology & visual science · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. Review

3 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

4 authors at 2 institutions in 1 country.

Abduqodir H ToychievDepartment of Ophthalmology, Weill Medical College of Cornell University, Burke Medical Research Institute, White Plains, New York 10605, USA.
Elena Ivanova
Christopher W Yee
Botir T Sagdullaev
Burke Medical Research Institute · USCornell University · US

Funding

Retinal neural processing during retinal degenerative diseasesR01EY020535 · NEI · WINIFRED MASTERSON BURKE MED RES INST · PI SAGDULLAEV, BOTIR T. · 2010 to 2014
$2.4M
NEI NIH HHS R01 EY020535NEI NIH HHS R01-EY020535
6 · The paper itself

Abstract

Retinal degeneration leads to progressive photoreceptor cell death, resulting in vision loss. Subsequently, inner retinal neurons develop aberrant synaptic activity, compounding visual impairment. In retinal ganglion cells, light responses driven by surviving photoreceptors are obscured by elevated levels of aberrant spiking activity. Here, we demonstrate in rd10 mice that targeting disruptive neuronal circuitry with a gap junction antagonist can significantly reduce excessive spiking. This treatment increases the sensitivity of the degenerated retina to light stimuli driven by residual photoreceptors. Additionally, this enhances signal transmission from inner retinal neurons to ganglion cells, potentially allowing the retinal network to preserve the fidelity of signals either from prosthetic electronic devices, or from cells optogenetically modified to transduce light. Thus, targeting maladaptive changes to the retina allows for treatments to use existing neuronal tissue to restore light sensitivity, and to augment existing strategies to replace lost photoreceptors.

Indexed as

Action PotentialsAnimalsCyclic Nucleotide Phosphodiesterases, Type 6Excitatory Postsynaptic PotentialsGap JunctionsIn Vitro TechniquesLightLight Signal TransductionMeclofenamic AcidMiceMice, TransgenicPhotoreceptor CellsRetinal DegenerationRetinal Ganglion CellsVision, OcularCyclic Nucleotide Phosphodiesterases, Type 6Meclofenamic AcidPde6b protein, mouse

Identifiers

PMID23986234
PMCPMC3756747
OpenAlexW2006028506

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.