Evidence map›Paper›PMID 28898257›Full record

ArticlePloS one2017

Transiency of retinal ganglion cell action potential responses determined by PSTH time constant.

Alma Ganczer, Márton Balogh, László Albert, Gábor Debertin, Tamás Kovács-Öller, Béla Völgyi

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Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

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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

3 citing papers in PubMed.

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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

6 authors.

Alma GanczerMTA-PTE NAP B Retinal Electrical Synapses Research Group, Pécs, Hungary.
Márton BaloghMTA-PTE NAP B Retinal Electrical Synapses Research Group, Pécs, Hungary.
László AlbertMTA-PTE NAP B Retinal Electrical Synapses Research Group, Pécs, Hungary.
Gábor DebertinMTA-PTE NAP B Retinal Electrical Synapses Research Group, Pécs, Hungary.
Tamás Kovács-ÖllerMTA-PTE NAP B Retinal Electrical Synapses Research Group, Pécs, Hungary.
Béla VölgyiMTA-PTE NAP B Retinal Electrical Synapses Research Group, Pécs, Hungary.ORCID http://orcid.org/0000-0001-7481-390X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinal ganglion cells (RGC) have been described to react to light stimuli either by producing short bursts of spikes or by maintaining a longer, continuous train of action potentials. Fast, quickly decaying responses are considered to be transient in nature and encode information about movement and direction, while cell responses that show a slow, drawn-out response fall into the sustained category and are thought to be responsible for carrying information related to color and contrast. Multiple approaches have been introduced thus far to measure and determine response transiency. In this study, we adopted and slightly modified a method described by Zeck and Masland to characterize RGC response transiency values and compare them to those obtained by alternative methods. As the first step, RGC spike responses were elicited by light stimulation and peristimulus time histograms (PSTHs) were generated. PSTHs then were used to calculate the time constant (PSTHτ approach). We show that this method is comparable to or more reliable than alternative approaches to describe the temporal characteristics of RGC light responses. In addition, we also show that PSTHτ-s are compatible with time constants measured on RGC and/or bipolar cell graded potentials; thus they are suitable for studying signaling through parallel retinal pathways.

Indexed as

Action PotentialsAnimalsExtracellular SpaceIntracellular SpaceLightMicePhotic StimulationReproducibility of ResultsRetinal Ganglion CellsSignal Transduction

Identifiers

PMID28898257
PMCPMC5595288

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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.