Temporal Sensitivity for Achromatic and Chromatic Flicker across the Visual Cortex
The retinal ganglion cells (RGCs) receive different combinations of L, M, and S cone inputs and give rise to one achromatic and two chromatic postreceptoral channels. The goal of the current study was to determine temporal sensitivity across the three postreceptoral channels in subcortical and corti...
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description | The retinal ganglion cells (RGCs) receive different combinations of L, M, and S cone inputs and give rise to one achromatic and two chromatic postreceptoral channels. The goal of the current study was to determine temporal sensitivity across the three postreceptoral channels in subcortical and cortical regions involved in human vision. We measured functional magnetic resonance imaging (fMRI) responses at 7 T from three participants (two males, one female) viewing a high-contrast, flickering, spatially uniform wide field (∼140°). 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 of the primary visual cortex (V1) across eccentricity and spatially averaged responses from the lateral geniculate nucleus (LGN), and the V2/V3, hV4, and V3A/B regions. fMRI responses reflected the known properties of the visual system, including higher peak temporal sensitivity to achromatic versus chromatic stimuli and low-pass filtering between the LGN and V1. Peak temporal sensitivity increased across levels of the cortical visual hierarchy. Unexpectedly, peak temporal sensitivity varied little across eccentricity within area V1. Measures of adaptation and distributed pattern activity revealed a subtle influence of 64 Hz achromatic flicker in area V1, despite this stimulus evoking only a minimal overall response. The comparison of measured cortical responses to a model of the integrated retinal output to our stimuli demonstrates that extensive filtering and amplification are applied to postretinal signals. |
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The goal of the current study was to determine temporal sensitivity across the three postreceptoral channels in subcortical and cortical regions involved in human vision. We measured functional magnetic resonance imaging (fMRI) responses at 7 T from three participants (two males, one female) viewing a high-contrast, flickering, spatially uniform wide field (∼140°). 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 of the primary visual cortex (V1) across eccentricity and spatially averaged responses from the lateral geniculate nucleus (LGN), and the V2/V3, hV4, and V3A/B regions. fMRI responses reflected the known properties of the visual system, including higher peak temporal sensitivity to achromatic versus chromatic stimuli and low-pass filtering between the LGN and V1. Peak temporal sensitivity increased across levels of the cortical visual hierarchy. Unexpectedly, peak temporal sensitivity varied little across eccentricity within area V1. Measures of adaptation and distributed pattern activity revealed a subtle influence of 64 Hz achromatic flicker in area V1, despite this stimulus evoking only a minimal overall response. The comparison of measured cortical responses to a model of the integrated retinal output to our stimuli demonstrates that extensive filtering and amplification are applied to postretinal signals.</description><identifier>ISSN: 0270-6474</identifier><identifier>ISSN: 1529-2401</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.1395-23.2024</identifier><identifier>PMID: 38621997</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Adult ; Channels ; Color Perception - physiology ; Contrast Sensitivity - physiology ; Eccentricity ; Female ; Flicker ; Functional magnetic resonance imaging ; Geniculate Bodies - physiology ; Humans ; Lateral geniculate nucleus ; Low pass filters ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Male ; Neuroimaging ; Photic Stimulation - methods ; Retina ; Retinal ganglion cells ; Sensitivity ; Stimuli ; Temporal lobe ; Visual cortex ; Visual Cortex - diagnostic imaging ; Visual Cortex - physiology ; Visual Pathways - diagnostic imaging ; Visual Pathways - physiology ; Visual system ; Young Adult</subject><ispartof>The Journal of neuroscience, 2024-05, Vol.44 (21), p.e1395232024</ispartof><rights>Copyright © 2024 the authors.</rights><rights>Copyright Society for Neuroscience May 22, 2024</rights><rights>Copyright © 2024 the authors 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c390t-134b50e500aaf6b458e183a9bfb97ab44a8895d0cacdc5203c654c7ce4fc0d13</cites><orcidid>0000-0002-4028-3100 ; 0000-0003-4996-2457</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11112647/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11112647/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38621997$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Patterson Gentile, Carlyn</creatorcontrib><creatorcontrib>Spitschan, Manuel</creatorcontrib><creatorcontrib>Taskin, Huseyin O</creatorcontrib><creatorcontrib>Bock, Andrew S</creatorcontrib><creatorcontrib>Aguirre, Geoffrey K</creatorcontrib><title>Temporal Sensitivity for Achromatic and Chromatic Flicker across the Visual Cortex</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>The retinal ganglion cells (RGCs) receive different combinations of L, M, and S cone inputs and give rise to one achromatic and two chromatic postreceptoral channels. The goal of the current study was to determine temporal sensitivity across the three postreceptoral channels in subcortical and cortical regions involved in human vision. We measured functional magnetic resonance imaging (fMRI) responses at 7 T from three participants (two males, one female) viewing a high-contrast, flickering, spatially uniform wide field (∼140°). 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 of the primary visual cortex (V1) across eccentricity and spatially averaged responses from the lateral geniculate nucleus (LGN), and the V2/V3, hV4, and V3A/B regions. fMRI responses reflected the known properties of the visual system, including higher peak temporal sensitivity to achromatic versus chromatic stimuli and low-pass filtering between the LGN and V1. Peak temporal sensitivity increased across levels of the cortical visual hierarchy. Unexpectedly, peak temporal sensitivity varied little across eccentricity within area V1. Measures of adaptation and distributed pattern activity revealed a subtle influence of 64 Hz achromatic flicker in area V1, despite this stimulus evoking only a minimal overall response. The comparison of measured cortical responses to a model of the integrated retinal output to our stimuli demonstrates that extensive filtering and amplification are applied to postretinal signals.</description><subject>Adult</subject><subject>Channels</subject><subject>Color Perception - physiology</subject><subject>Contrast Sensitivity - physiology</subject><subject>Eccentricity</subject><subject>Female</subject><subject>Flicker</subject><subject>Functional magnetic resonance imaging</subject><subject>Geniculate Bodies - physiology</subject><subject>Humans</subject><subject>Lateral geniculate nucleus</subject><subject>Low pass filters</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Neuroimaging</subject><subject>Photic Stimulation - methods</subject><subject>Retina</subject><subject>Retinal ganglion cells</subject><subject>Sensitivity</subject><subject>Stimuli</subject><subject>Temporal lobe</subject><subject>Visual cortex</subject><subject>Visual Cortex - diagnostic imaging</subject><subject>Visual Cortex - physiology</subject><subject>Visual Pathways - diagnostic imaging</subject><subject>Visual Pathways - physiology</subject><subject>Visual system</subject><subject>Young Adult</subject><issn>0270-6474</issn><issn>1529-2401</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkVtP3DAQhS3UCpYtfwFF6ktfsh1fEz9VKIJChYq0LLxajuOwpkm8tRME_75eLiuoXyx7zhzNmQ-hYwwLzAn9_uv36c3y6rq6WGAqeU7oggBhe2iWqjInDPAnNANSQC5YwQ7QYYz3AFAALvbRAS0FwVIWM7Rc2X7jg-6yaztEN7oHNz5lrQ_ZiVkH3-vRmUwPTVbtXmedM39syLQJPsZsXNvs1sUpWVQ-jPbxC_rc6i7ao9d7jlZnp6vqPL-8-nlRnVzmhkoYc0xZzcFyAK1bUTNeWlxSLeu2loWuGdNlKXkDRpvGcALUCM5MYSxrDTSYztGPF9vNVPe2MXYYUwy1Ca7X4Ul57dTHyuDW6s4_KJwOSVtJDt9eHYL_O9k4qt5FY7tOD9ZPUVGgsoRSCJqkX_-T3vspDCleUnEpBRWCJ5V4UT1vJth2Nw0GtcWmdtjUFptKP1tsqfH4fZZd2xsn-g_YkZXJ</recordid><startdate>20240522</startdate><enddate>20240522</enddate><creator>Patterson Gentile, Carlyn</creator><creator>Spitschan, Manuel</creator><creator>Taskin, Huseyin O</creator><creator>Bock, Andrew S</creator><creator>Aguirre, Geoffrey K</creator><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4028-3100</orcidid><orcidid>https://orcid.org/0000-0003-4996-2457</orcidid></search><sort><creationdate>20240522</creationdate><title>Temporal Sensitivity for Achromatic and Chromatic Flicker across the Visual Cortex</title><author>Patterson Gentile, Carlyn ; Spitschan, Manuel ; Taskin, Huseyin O ; Bock, Andrew S ; Aguirre, Geoffrey K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-134b50e500aaf6b458e183a9bfb97ab44a8895d0cacdc5203c654c7ce4fc0d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Channels</topic><topic>Color Perception - physiology</topic><topic>Contrast Sensitivity - physiology</topic><topic>Eccentricity</topic><topic>Female</topic><topic>Flicker</topic><topic>Functional magnetic resonance imaging</topic><topic>Geniculate Bodies - physiology</topic><topic>Humans</topic><topic>Lateral geniculate nucleus</topic><topic>Low pass filters</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Neuroimaging</topic><topic>Photic Stimulation - methods</topic><topic>Retina</topic><topic>Retinal ganglion cells</topic><topic>Sensitivity</topic><topic>Stimuli</topic><topic>Temporal lobe</topic><topic>Visual cortex</topic><topic>Visual Cortex - diagnostic imaging</topic><topic>Visual Cortex - physiology</topic><topic>Visual Pathways - diagnostic imaging</topic><topic>Visual Pathways - physiology</topic><topic>Visual system</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Patterson Gentile, Carlyn</creatorcontrib><creatorcontrib>Spitschan, Manuel</creatorcontrib><creatorcontrib>Taskin, Huseyin O</creatorcontrib><creatorcontrib>Bock, Andrew S</creatorcontrib><creatorcontrib>Aguirre, Geoffrey K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patterson Gentile, Carlyn</au><au>Spitschan, Manuel</au><au>Taskin, Huseyin O</au><au>Bock, Andrew S</au><au>Aguirre, Geoffrey K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Temporal Sensitivity for Achromatic and Chromatic Flicker across the Visual Cortex</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2024-05-22</date><risdate>2024</risdate><volume>44</volume><issue>21</issue><spage>e1395232024</spage><pages>e1395232024-</pages><issn>0270-6474</issn><issn>1529-2401</issn><eissn>1529-2401</eissn><abstract>The retinal ganglion cells (RGCs) receive different combinations of L, M, and S cone inputs and give rise to one achromatic and two chromatic postreceptoral channels. The goal of the current study was to determine temporal sensitivity across the three postreceptoral channels in subcortical and cortical regions involved in human vision. We measured functional magnetic resonance imaging (fMRI) responses at 7 T from three participants (two males, one female) viewing a high-contrast, flickering, spatially uniform wide field (∼140°). 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 of the primary visual cortex (V1) across eccentricity and spatially averaged responses from the lateral geniculate nucleus (LGN), and the V2/V3, hV4, and V3A/B regions. fMRI responses reflected the known properties of the visual system, including higher peak temporal sensitivity to achromatic versus chromatic stimuli and low-pass filtering between the LGN and V1. Peak temporal sensitivity increased across levels of the cortical visual hierarchy. Unexpectedly, peak temporal sensitivity varied little across eccentricity within area V1. Measures of adaptation and distributed pattern activity revealed a subtle influence of 64 Hz achromatic flicker in area V1, despite this stimulus evoking only a minimal overall response. The comparison of measured cortical responses to a model of the integrated retinal output to our stimuli demonstrates that extensive filtering and amplification are applied to postretinal signals.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>38621997</pmid><doi>10.1523/JNEUROSCI.1395-23.2024</doi><orcidid>https://orcid.org/0000-0002-4028-3100</orcidid><orcidid>https://orcid.org/0000-0003-4996-2457</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Channels Color Perception - physiology Contrast Sensitivity - physiology Eccentricity Female Flicker Functional magnetic resonance imaging Geniculate Bodies - physiology Humans Lateral geniculate nucleus Low pass filters Magnetic resonance imaging Magnetic Resonance Imaging - methods Male Neuroimaging Photic Stimulation - methods Retina Retinal ganglion cells Sensitivity Stimuli Temporal lobe Visual cortex Visual Cortex - diagnostic imaging Visual Cortex - physiology Visual Pathways - diagnostic imaging Visual Pathways - physiology Visual system Young Adult |
title | Temporal Sensitivity for Achromatic and Chromatic Flicker across the Visual Cortex |
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