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The Method of Silent Substitution for Examining Melanopsin Contributions to Pupil Control

The human pupillary light response is driven by all classes of photoreceptors in the human eye—the three classes of cones, the rods, and the intrinsically photosensitive retinal ganglion cells (ipRGCs) expressing the photopigment melanopsin. These photoreceptor classes have distinct but overlapping...

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Detalles Bibliográficos
Autores principales: Spitschan, Manuel, Woelders, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277556/
https://www.ncbi.nlm.nih.gov/pubmed/30538662
http://dx.doi.org/10.3389/fneur.2018.00941
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author Spitschan, Manuel
Woelders, Tom
author_facet Spitschan, Manuel
Woelders, Tom
author_sort Spitschan, Manuel
collection PubMed
description The human pupillary light response is driven by all classes of photoreceptors in the human eye—the three classes of cones, the rods, and the intrinsically photosensitive retinal ganglion cells (ipRGCs) expressing the photopigment melanopsin. These photoreceptor classes have distinct but overlapping spectral tuning, and even a monochromatic light with a wavelength matched to the peak spectral sensitivity of a given photoreceptor will stimulate all photoreceptors. The method of silent substitution uses pairs of lights (“metamers”) to selectively stimulate a given class of photoreceptors while keeping the activation of all others constant. In this primer, we describe the method of silent substitution and provide an overview of studies that have used it to examine inputs to the human pupillary light response.
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spelling pubmed-62775562018-12-11 The Method of Silent Substitution for Examining Melanopsin Contributions to Pupil Control Spitschan, Manuel Woelders, Tom Front Neurol Neurology The human pupillary light response is driven by all classes of photoreceptors in the human eye—the three classes of cones, the rods, and the intrinsically photosensitive retinal ganglion cells (ipRGCs) expressing the photopigment melanopsin. These photoreceptor classes have distinct but overlapping spectral tuning, and even a monochromatic light with a wavelength matched to the peak spectral sensitivity of a given photoreceptor will stimulate all photoreceptors. The method of silent substitution uses pairs of lights (“metamers”) to selectively stimulate a given class of photoreceptors while keeping the activation of all others constant. In this primer, we describe the method of silent substitution and provide an overview of studies that have used it to examine inputs to the human pupillary light response. Frontiers Media S.A. 2018-11-27 /pmc/articles/PMC6277556/ /pubmed/30538662 http://dx.doi.org/10.3389/fneur.2018.00941 Text en Copyright © 2018 Spitschan and Woelders. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Spitschan, Manuel
Woelders, Tom
The Method of Silent Substitution for Examining Melanopsin Contributions to Pupil Control
title The Method of Silent Substitution for Examining Melanopsin Contributions to Pupil Control
title_full The Method of Silent Substitution for Examining Melanopsin Contributions to Pupil Control
title_fullStr The Method of Silent Substitution for Examining Melanopsin Contributions to Pupil Control
title_full_unstemmed The Method of Silent Substitution for Examining Melanopsin Contributions to Pupil Control
title_short The Method of Silent Substitution for Examining Melanopsin Contributions to Pupil Control
title_sort method of silent substitution for examining melanopsin contributions to pupil control
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277556/
https://www.ncbi.nlm.nih.gov/pubmed/30538662
http://dx.doi.org/10.3389/fneur.2018.00941
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