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Quantification of the early pupillary dilation kinetic to assess rod and cone activity

Rods, cones and melanopsin contribute in various proportions, depending on the stimulus light, to the pupil light response. This study used a first derivative analysis to focus on the quantification of the dynamics of pupillary dilation that immediately follows light-induced pupilloconstriction in o...

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Autores principales: Kostic, Corinne, Crippa, Sylvain V., Leon, Lorette, Hamel, Christian, Meunier, Isabelle, Kawasaki, Aki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099900/
https://www.ncbi.nlm.nih.gov/pubmed/33953266
http://dx.doi.org/10.1038/s41598-021-88915-z
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author Kostic, Corinne
Crippa, Sylvain V.
Leon, Lorette
Hamel, Christian
Meunier, Isabelle
Kawasaki, Aki
author_facet Kostic, Corinne
Crippa, Sylvain V.
Leon, Lorette
Hamel, Christian
Meunier, Isabelle
Kawasaki, Aki
author_sort Kostic, Corinne
collection PubMed
description Rods, cones and melanopsin contribute in various proportions, depending on the stimulus light, to the pupil light response. This study used a first derivative analysis to focus on the quantification of the dynamics of pupillary dilation that immediately follows light-induced pupilloconstriction in order to identify novel parameters that reflect rod and cone activity. In 18 healthy adults, the pupil response to a 1 s blue light stimulus ranging from − 6.0 to 2.65 log cd/m(2) in dark-adapted conditions and to a 1 s blue light stimulus (2.65 log cd/m(2)) in light-adapted conditions was recorded on a customized pupillometer. Three derivative parameters which describe the 2.75 s following the light onset were quantified: dAMP (maximal amplitude of the positive peak), dLAT (latency of the positive peak), dAUC (area under the curve of the positive peak). We found that dAMP and dAUC but not dLAT have graded responses over a range of light intensities. The maximal positive value of dAMP, representing maximal rate of change of early pupillary dilation phase, occurs at − 1.0 log cd/m(2) and this stimulus intensity appears useful for activating rods and cones. From − 0.5 log cd/m(2) to brighter intensities dAMP and dAUC progressively decrease, reaching negligible values at 2.65 log cd/m(2) indicative of a melanopsin-driven pupil response that masks the contribution from rods and cones to the early phase of pupillary dilation.
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spelling pubmed-80999002021-05-07 Quantification of the early pupillary dilation kinetic to assess rod and cone activity Kostic, Corinne Crippa, Sylvain V. Leon, Lorette Hamel, Christian Meunier, Isabelle Kawasaki, Aki Sci Rep Article Rods, cones and melanopsin contribute in various proportions, depending on the stimulus light, to the pupil light response. This study used a first derivative analysis to focus on the quantification of the dynamics of pupillary dilation that immediately follows light-induced pupilloconstriction in order to identify novel parameters that reflect rod and cone activity. In 18 healthy adults, the pupil response to a 1 s blue light stimulus ranging from − 6.0 to 2.65 log cd/m(2) in dark-adapted conditions and to a 1 s blue light stimulus (2.65 log cd/m(2)) in light-adapted conditions was recorded on a customized pupillometer. Three derivative parameters which describe the 2.75 s following the light onset were quantified: dAMP (maximal amplitude of the positive peak), dLAT (latency of the positive peak), dAUC (area under the curve of the positive peak). We found that dAMP and dAUC but not dLAT have graded responses over a range of light intensities. The maximal positive value of dAMP, representing maximal rate of change of early pupillary dilation phase, occurs at − 1.0 log cd/m(2) and this stimulus intensity appears useful for activating rods and cones. From − 0.5 log cd/m(2) to brighter intensities dAMP and dAUC progressively decrease, reaching negligible values at 2.65 log cd/m(2) indicative of a melanopsin-driven pupil response that masks the contribution from rods and cones to the early phase of pupillary dilation. Nature Publishing Group UK 2021-05-05 /pmc/articles/PMC8099900/ /pubmed/33953266 http://dx.doi.org/10.1038/s41598-021-88915-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kostic, Corinne
Crippa, Sylvain V.
Leon, Lorette
Hamel, Christian
Meunier, Isabelle
Kawasaki, Aki
Quantification of the early pupillary dilation kinetic to assess rod and cone activity
title Quantification of the early pupillary dilation kinetic to assess rod and cone activity
title_full Quantification of the early pupillary dilation kinetic to assess rod and cone activity
title_fullStr Quantification of the early pupillary dilation kinetic to assess rod and cone activity
title_full_unstemmed Quantification of the early pupillary dilation kinetic to assess rod and cone activity
title_short Quantification of the early pupillary dilation kinetic to assess rod and cone activity
title_sort quantification of the early pupillary dilation kinetic to assess rod and cone activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099900/
https://www.ncbi.nlm.nih.gov/pubmed/33953266
http://dx.doi.org/10.1038/s41598-021-88915-z
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