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Melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision

To evaluate the nature of interactions between visual pathways transmitting the slower melanopsin and faster rod and cone signals, we implement a temporal phase summation paradigm in human observers using photoreceptor-directed stimuli. We show that melanopsin stimulation interacts with and alters b...

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Detalles Bibliográficos
Autores principales: Uprety, Samir, Adhikari, Prakash, Feigl, Beatrix, Zele, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218364/
https://www.ncbi.nlm.nih.gov/pubmed/35754721
http://dx.doi.org/10.1016/j.isci.2022.104529
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author Uprety, Samir
Adhikari, Prakash
Feigl, Beatrix
Zele, Andrew J.
author_facet Uprety, Samir
Adhikari, Prakash
Feigl, Beatrix
Zele, Andrew J.
author_sort Uprety, Samir
collection PubMed
description To evaluate the nature of interactions between visual pathways transmitting the slower melanopsin and faster rod and cone signals, we implement a temporal phase summation paradigm in human observers using photoreceptor-directed stimuli. We show that melanopsin stimulation interacts with and alters both rod-mediated and cone-mediated vision regardless of whether it is perceptually visible or not. Melanopsin-rod interactions result in either inhibitory or facilitatory summation depending on the temporal frequency and photoreceptor pathway contrast sensitivity. Moreover, by isolating rod vision, we reveal a bipartite intensity response property of the rod pathway in photopic lighting that extends its operational range at lower frequencies to beyond its classic saturation limits but at the expense of attenuating sensitivity at higher frequencies. In comparison, melanopsin-cone interactions always lead to facilitation. These interactions can be described by linear or probability summations and potentially involve multiple intraretinal and visual cortical pathways to set human visual contrast sensitivity.
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spelling pubmed-92183642022-06-24 Melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision Uprety, Samir Adhikari, Prakash Feigl, Beatrix Zele, Andrew J. iScience Article To evaluate the nature of interactions between visual pathways transmitting the slower melanopsin and faster rod and cone signals, we implement a temporal phase summation paradigm in human observers using photoreceptor-directed stimuli. We show that melanopsin stimulation interacts with and alters both rod-mediated and cone-mediated vision regardless of whether it is perceptually visible or not. Melanopsin-rod interactions result in either inhibitory or facilitatory summation depending on the temporal frequency and photoreceptor pathway contrast sensitivity. Moreover, by isolating rod vision, we reveal a bipartite intensity response property of the rod pathway in photopic lighting that extends its operational range at lower frequencies to beyond its classic saturation limits but at the expense of attenuating sensitivity at higher frequencies. In comparison, melanopsin-cone interactions always lead to facilitation. These interactions can be described by linear or probability summations and potentially involve multiple intraretinal and visual cortical pathways to set human visual contrast sensitivity. Elsevier 2022-06-03 /pmc/articles/PMC9218364/ /pubmed/35754721 http://dx.doi.org/10.1016/j.isci.2022.104529 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Uprety, Samir
Adhikari, Prakash
Feigl, Beatrix
Zele, Andrew J.
Melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision
title Melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision
title_full Melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision
title_fullStr Melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision
title_full_unstemmed Melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision
title_short Melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision
title_sort melanopsin photoreception differentially modulates rod-mediated and cone-mediated human temporal vision
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218364/
https://www.ncbi.nlm.nih.gov/pubmed/35754721
http://dx.doi.org/10.1016/j.isci.2022.104529
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