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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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. |
format | Online Article Text |
id | pubmed-9218364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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