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The morphology of human rod ERGs obtained by silent substitution stimulation

PURPOSE: To record transient ERGs from the light-adapted human retina using silent substitution stimuli which selectively reflect the activity of rod photoreceptors. We aim to describe the morphology of these waveforms and examine how they are affected by the use of less selective stimuli and by ret...

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Autores principales: Maguire, J., Parry, N. R. A., Kremers, J., Murray, I. J., McKeefry, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5274650/
https://www.ncbi.nlm.nih.gov/pubmed/28091887
http://dx.doi.org/10.1007/s10633-017-9571-4
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author Maguire, J.
Parry, N. R. A.
Kremers, J.
Murray, I. J.
McKeefry, D.
author_facet Maguire, J.
Parry, N. R. A.
Kremers, J.
Murray, I. J.
McKeefry, D.
author_sort Maguire, J.
collection PubMed
description PURPOSE: To record transient ERGs from the light-adapted human retina using silent substitution stimuli which selectively reflect the activity of rod photoreceptors. We aim to describe the morphology of these waveforms and examine how they are affected by the use of less selective stimuli and by retinal pathology. METHODS: Rod-isolating stimuli with square-wave temporal profiles (250/250 ms onset/offset) were presented using a 4 primary LED ganzfeld stimulator. Experiment 1: ERGs were recorded using a rod-isolating stimulus (63 ph Td, rod contrast, C (rod) = 0.25) from a group (n = 20) of normal trichromatic observers. Experiment 2: Rod ERGs were recorded from a group (n = 5) using a rod-isolating stimulus (C (rod) = 0.25) which varied in retinal illuminance from 40 to 10,000 ph Td. Experiment 3: ERGs were elicited using 2 kinds of non-isolating stimuli; (1) broadband and (2) rod-isolating stimuli which contained varying degrees of L- and M-cone excitation. Experiment 4: Rod ERGs were recorded from two patient groups with rod monochromacy (n = 3) and CSNB (type 1; n = 2). RESULTS: The rod-isolated ERGs elicited from normal subjects had a waveform with a positive onset component followed by a negative offset. Response amplitude was maximal at retinal illuminances <100 ph Td and was virtually abolished at 400 ph Td. The use of non-selective stimuli altered the ERG waveform eliciting more photopic-like ERG responses. Rod ERGs recorded from rod monochromats had similar features to those recorded from normal trichromats, in contrast to those recorded from participants with CSNB which had an electronegative appearance. CONCLUSIONS: Our results demonstrate that ERGs elicited by silent substitution stimuli can selectively reflect the operation of rod photoreceptors in the normal, light-adapted human retina.
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spelling pubmed-52746502017-02-10 The morphology of human rod ERGs obtained by silent substitution stimulation Maguire, J. Parry, N. R. A. Kremers, J. Murray, I. J. McKeefry, D. Doc Ophthalmol Original Research Article PURPOSE: To record transient ERGs from the light-adapted human retina using silent substitution stimuli which selectively reflect the activity of rod photoreceptors. We aim to describe the morphology of these waveforms and examine how they are affected by the use of less selective stimuli and by retinal pathology. METHODS: Rod-isolating stimuli with square-wave temporal profiles (250/250 ms onset/offset) were presented using a 4 primary LED ganzfeld stimulator. Experiment 1: ERGs were recorded using a rod-isolating stimulus (63 ph Td, rod contrast, C (rod) = 0.25) from a group (n = 20) of normal trichromatic observers. Experiment 2: Rod ERGs were recorded from a group (n = 5) using a rod-isolating stimulus (C (rod) = 0.25) which varied in retinal illuminance from 40 to 10,000 ph Td. Experiment 3: ERGs were elicited using 2 kinds of non-isolating stimuli; (1) broadband and (2) rod-isolating stimuli which contained varying degrees of L- and M-cone excitation. Experiment 4: Rod ERGs were recorded from two patient groups with rod monochromacy (n = 3) and CSNB (type 1; n = 2). RESULTS: The rod-isolated ERGs elicited from normal subjects had a waveform with a positive onset component followed by a negative offset. Response amplitude was maximal at retinal illuminances <100 ph Td and was virtually abolished at 400 ph Td. The use of non-selective stimuli altered the ERG waveform eliciting more photopic-like ERG responses. Rod ERGs recorded from rod monochromats had similar features to those recorded from normal trichromats, in contrast to those recorded from participants with CSNB which had an electronegative appearance. CONCLUSIONS: Our results demonstrate that ERGs elicited by silent substitution stimuli can selectively reflect the operation of rod photoreceptors in the normal, light-adapted human retina. Springer Berlin Heidelberg 2017-01-13 2017 /pmc/articles/PMC5274650/ /pubmed/28091887 http://dx.doi.org/10.1007/s10633-017-9571-4 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research Article
Maguire, J.
Parry, N. R. A.
Kremers, J.
Murray, I. J.
McKeefry, D.
The morphology of human rod ERGs obtained by silent substitution stimulation
title The morphology of human rod ERGs obtained by silent substitution stimulation
title_full The morphology of human rod ERGs obtained by silent substitution stimulation
title_fullStr The morphology of human rod ERGs obtained by silent substitution stimulation
title_full_unstemmed The morphology of human rod ERGs obtained by silent substitution stimulation
title_short The morphology of human rod ERGs obtained by silent substitution stimulation
title_sort morphology of human rod ergs obtained by silent substitution stimulation
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5274650/
https://www.ncbi.nlm.nih.gov/pubmed/28091887
http://dx.doi.org/10.1007/s10633-017-9571-4
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