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Temporal sensitivity for achromatic and chromatic flicker across the visual cortex

The classes of retinal ganglion cells (RGCs) receive different combinations of L, M, and S cone inputs and give rise to one achromatic and two chromatic post-receptoral channels. Beyond the retina, RGC outputs are subject to filtering and normalization along the geniculo-striate pathway, ultimately...

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Autores principales: Gentile, Carlyn Patterson, Spitschan, Manuel, Taskin, Huseyin O., Bock, Andrew S., Aguirre, Geoffrey K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402088/
https://www.ncbi.nlm.nih.gov/pubmed/37546951
http://dx.doi.org/10.1101/2023.07.24.550403
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author Gentile, Carlyn Patterson
Spitschan, Manuel
Taskin, Huseyin O.
Bock, Andrew S.
Aguirre, Geoffrey K.
author_facet Gentile, Carlyn Patterson
Spitschan, Manuel
Taskin, Huseyin O.
Bock, Andrew S.
Aguirre, Geoffrey K.
author_sort Gentile, Carlyn Patterson
collection PubMed
description The classes of retinal ganglion cells (RGCs) receive different combinations of L, M, and S cone inputs and give rise to one achromatic and two chromatic post-receptoral channels. Beyond the retina, RGC outputs are subject to filtering and normalization along the geniculo-striate pathway, ultimately producing the properties of human vision. The goal of the current study was to determine temporal sensitivity across the three post-receptoral channels in subcortical and cortical regions involved in vision, to better characterize post-retinal temporal processing. We measured functional magnetic resonance imaging (MRI) responses at 7 Tesla from participants viewing a high-contrast, flickering, spatially-uniform wide (~140°) field. Stimulus flicker frequency varied logarithmically between 2 and 64 Hz and targeted the L+M+S, L–M, and S–[L+M] cone combinations. These measurements were used to create temporal sensitivity functions (TSFs) of primary visual cortex (V1) across eccentricity, and spatially averaged responses from lateral geniculate nucleus (LGN), V2/V3, hV4, and MT. Functional MRI responses reflected known properties of the visual system, including higher peak temporal sensitivity to achromatic vs. chromatic stimuli, and low-pass filtering between the LGN and V1. V1 had the slowest peak temporal sensitivity across cortical regions, which increased at higher levels of the visual cortical hierarchy. Unexpectedly, peak temporal sensitivity decreased at greater eccentricities in area V1, especially for achromatic stimuli. Comparison of measured cortical responses to a model of integrated retinal output to our stimuli demonstrates that extensive filtering and amplification is applied to post-retinal signals.
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spelling pubmed-104020882023-08-05 Temporal sensitivity for achromatic and chromatic flicker across the visual cortex Gentile, Carlyn Patterson Spitschan, Manuel Taskin, Huseyin O. Bock, Andrew S. Aguirre, Geoffrey K. bioRxiv Article The classes of retinal ganglion cells (RGCs) receive different combinations of L, M, and S cone inputs and give rise to one achromatic and two chromatic post-receptoral channels. Beyond the retina, RGC outputs are subject to filtering and normalization along the geniculo-striate pathway, ultimately producing the properties of human vision. The goal of the current study was to determine temporal sensitivity across the three post-receptoral channels in subcortical and cortical regions involved in vision, to better characterize post-retinal temporal processing. We measured functional magnetic resonance imaging (MRI) responses at 7 Tesla from participants viewing a high-contrast, flickering, spatially-uniform wide (~140°) field. Stimulus flicker frequency varied logarithmically between 2 and 64 Hz and targeted the L+M+S, L–M, and S–[L+M] cone combinations. These measurements were used to create temporal sensitivity functions (TSFs) of primary visual cortex (V1) across eccentricity, and spatially averaged responses from lateral geniculate nucleus (LGN), V2/V3, hV4, and MT. Functional MRI responses reflected known properties of the visual system, including higher peak temporal sensitivity to achromatic vs. chromatic stimuli, and low-pass filtering between the LGN and V1. V1 had the slowest peak temporal sensitivity across cortical regions, which increased at higher levels of the visual cortical hierarchy. Unexpectedly, peak temporal sensitivity decreased at greater eccentricities in area V1, especially for achromatic stimuli. Comparison of measured cortical responses to a model of integrated retinal output to our stimuli demonstrates that extensive filtering and amplification is applied to post-retinal signals. Cold Spring Harbor Laboratory 2023-07-26 /pmc/articles/PMC10402088/ /pubmed/37546951 http://dx.doi.org/10.1101/2023.07.24.550403 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Gentile, Carlyn Patterson
Spitschan, Manuel
Taskin, Huseyin O.
Bock, Andrew S.
Aguirre, Geoffrey K.
Temporal sensitivity for achromatic and chromatic flicker across the visual cortex
title Temporal sensitivity for achromatic and chromatic flicker across the visual cortex
title_full Temporal sensitivity for achromatic and chromatic flicker across the visual cortex
title_fullStr Temporal sensitivity for achromatic and chromatic flicker across the visual cortex
title_full_unstemmed Temporal sensitivity for achromatic and chromatic flicker across the visual cortex
title_short Temporal sensitivity for achromatic and chromatic flicker across the visual cortex
title_sort temporal sensitivity for achromatic and chromatic flicker across the visual cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402088/
https://www.ncbi.nlm.nih.gov/pubmed/37546951
http://dx.doi.org/10.1101/2023.07.24.550403
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