Evidence map›Paper›PMID 29862172›Full record

ArticleInternational journal of ophthalmology2018

Changes in intrinsic excitability of ganglion cells in degenerated retinas of RCS rats.

Yi-Ming Ren, Chuan-Huang Weng, Cong-Jian Zhao, Zheng-Qin Yin

Open access · goldAbstract read
In one paragraph

Article in International journal of ophthalmology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. High-Fidelity Reproduction of Visual Signals by Electrical Stimulation in the Central Primate Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  4. Article
  5. Article
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  8. Review
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.

Yi-Ming RenSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Army Medical University); Key Lab of Visual Damage and Regeneration & Restoration of Chongqing, Chongqing 400038, China.
Chuan-Huang WengSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Army Medical University); Key Lab of Visual Damage and Regeneration & Restoration of Chongqing, Chongqing 400038, China.
Cong-Jian ZhaoSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Army Medical University); Key Lab of Visual Damage and Regeneration & Restoration of Chongqing, Chongqing 400038, China.
Zheng-Qin YinSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Army Medical University); Key Lab of Visual Damage and Regeneration & Restoration of Chongqing, Chongqing 400038, China.
Army Medical University · CNSouthwest Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo evaluate the intrinsic excitability of retinal ganglion cells (RGCs) in degenerated retinas.

methodsThe intrinsic excitability of various morphologically defined RGC types using a combination of patch-clamp recording and the Lucifer yellow tracer in retinal whole-mount preparations harvested from Royal College of Surgeons (RCS) rats, a common retinitis pigmentosa (RP) model, in a relatively late stage of retinal degeneration (P90) were investigated. Several parameters of RGC morphologies and action potentials (APs) were measured and compared to those of non-dystrophic control rats, including dendritic stratification, dendritic field diameter, peak amplitude, half width, resting membrane potential, AP threshold, depolarization to threshold, and firing rates.

resultsCompared with non-dystrophic control RGCs, more depolarizations were required to reach the AP threshold in RCS RGCs with low spontaneous spike rates and in RCS OFF cells (especially A2o cells), and RCS RGCs maintained their dendritic morphologies, resting membrane potentials and capabilities to generate APs.

conclusionRGCs are relatively well preserved morphologically and functionally, and some cells are more susceptible to decreased excitability during retinal degeneration. These findings provide valuable considerations for optimizing RP therapeutic strategies.

Indexed as

ganglion cellintrinsic excitabilitypatch clampretinal degeneration

Identifiers

PMID29862172
PMCPMC5957025
OpenAlexW2883188422

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.