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Transiency of retinal ganglion cell action potential responses determined by PSTH time constant
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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595288/ https://www.ncbi.nlm.nih.gov/pubmed/28898257 http://dx.doi.org/10.1371/journal.pone.0183436 |
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author | Ganczer, Alma Balogh, Márton Albert, László Debertin, Gábor Kovács-Öller, Tamás Völgyi, Béla |
author_facet | Ganczer, Alma Balogh, Márton Albert, László Debertin, Gábor Kovács-Öller, Tamás Völgyi, Béla |
author_sort | Ganczer, Alma |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5595288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55952882017-09-15 Transiency of retinal ganglion cell action potential responses determined by PSTH time constant Ganczer, Alma Balogh, Márton Albert, László Debertin, Gábor Kovács-Öller, Tamás Völgyi, Béla PLoS One Research Article 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. Public Library of Science 2017-09-12 /pmc/articles/PMC5595288/ /pubmed/28898257 http://dx.doi.org/10.1371/journal.pone.0183436 Text en © 2017 Ganczer et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ganczer, Alma Balogh, Márton Albert, László Debertin, Gábor Kovács-Öller, Tamás Völgyi, Béla Transiency of retinal ganglion cell action potential responses determined by PSTH time constant |
title | Transiency of retinal ganglion cell action potential responses determined by PSTH time constant |
title_full | Transiency of retinal ganglion cell action potential responses determined by PSTH time constant |
title_fullStr | Transiency of retinal ganglion cell action potential responses determined by PSTH time constant |
title_full_unstemmed | Transiency of retinal ganglion cell action potential responses determined by PSTH time constant |
title_short | Transiency of retinal ganglion cell action potential responses determined by PSTH time constant |
title_sort | transiency of retinal ganglion cell action potential responses determined by psth time constant |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595288/ https://www.ncbi.nlm.nih.gov/pubmed/28898257 http://dx.doi.org/10.1371/journal.pone.0183436 |
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