Melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flicker

Abstract In addition to the rod and cone photoreceptors the retina contains intrinsically photosensitive retinal ganglion cells (ipRGCs). These cells express the photopigment melanopsin and are known to be involved in reflexive visual functions such as pupil response and photo-entrainment of the cir...

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Main Authors: Joris Vincent, Edda B. Haggerty, David H. Brainard, Geoffrey K. Aguirre
Format: Article
Language:English
Published: Nature Portfolio 2021-10-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-99684-0
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author Joris Vincent
Edda B. Haggerty
David H. Brainard
Geoffrey K. Aguirre
author_facet Joris Vincent
Edda B. Haggerty
David H. Brainard
Geoffrey K. Aguirre
author_sort Joris Vincent
collection DOAJ
description Abstract In addition to the rod and cone photoreceptors the retina contains intrinsically photosensitive retinal ganglion cells (ipRGCs). These cells express the photopigment melanopsin and are known to be involved in reflexive visual functions such as pupil response and photo-entrainment of the circadian rhythm. It is possible that the ipRGCs contribute to conscious visual perception, either by providing an independent signal to the geniculo-striate pathway, or by interacting with and thus modifying signals arising from “classical” retinal ganglion cells that combine and contrast cone input. Here, we tested for the existence of an interaction by asking if a 350% change in melanopsin stimulation alters psychophysical sensitivity for the detection of luminance flicker. In Experiment 1, we tested for a change in the threshold for detecting luminance flicker in three participants after they adapted to backgrounds with different degrees of tonic melanopsin stimulation. In Experiments 2 and 3, this test was repeated, but now for luminance flicker presented on a transient pedestal of melanopsin stimulation. Across the three experiments, no effect of melanopsin stimulation upon threshold flicker sensitivity was found. Our results suggest that even large changes in melanopsin stimulation do not affect near-threshold, cone-mediated visual perception.
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spelling doaj.art-338046f7ca8446508a1c262008d8e0012022-12-21T18:23:43ZengNature PortfolioScientific Reports2045-23222021-10-0111111510.1038/s41598-021-99684-0Melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flickerJoris Vincent0Edda B. Haggerty1David H. Brainard2Geoffrey K. Aguirre3Computational Psychology, Institute of Computer Engineering and Microelectronics, Technische Universität BerlinDepartment of Neurology, Perelman School of Medicine, University of PennsylvaniaDepartment of Psychology, School of Arts and Sciences, University of PennsylvaniaDepartment of Neurology, Perelman School of Medicine, University of PennsylvaniaAbstract In addition to the rod and cone photoreceptors the retina contains intrinsically photosensitive retinal ganglion cells (ipRGCs). These cells express the photopigment melanopsin and are known to be involved in reflexive visual functions such as pupil response and photo-entrainment of the circadian rhythm. It is possible that the ipRGCs contribute to conscious visual perception, either by providing an independent signal to the geniculo-striate pathway, or by interacting with and thus modifying signals arising from “classical” retinal ganglion cells that combine and contrast cone input. Here, we tested for the existence of an interaction by asking if a 350% change in melanopsin stimulation alters psychophysical sensitivity for the detection of luminance flicker. In Experiment 1, we tested for a change in the threshold for detecting luminance flicker in three participants after they adapted to backgrounds with different degrees of tonic melanopsin stimulation. In Experiments 2 and 3, this test was repeated, but now for luminance flicker presented on a transient pedestal of melanopsin stimulation. Across the three experiments, no effect of melanopsin stimulation upon threshold flicker sensitivity was found. Our results suggest that even large changes in melanopsin stimulation do not affect near-threshold, cone-mediated visual perception.https://doi.org/10.1038/s41598-021-99684-0
spellingShingle Joris Vincent
Edda B. Haggerty
David H. Brainard
Geoffrey K. Aguirre
Melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flicker
Scientific Reports
title Melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flicker
title_full Melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flicker
title_fullStr Melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flicker
title_full_unstemmed Melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flicker
title_short Melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flicker
title_sort melanopic stimulation does not alter psychophysical threshold sensitivity for luminance flicker
url https://doi.org/10.1038/s41598-021-99684-0
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AT geoffreykaguirre melanopicstimulationdoesnotalterpsychophysicalthresholdsensitivityforluminanceflicker