Separable pupillary signatures of perception and action during perceptual multistability

The pupil provides a rich, non-invasive measure of the neural bases of perception and cognition and has been of particular value in uncovering the role of arousal-linked neuromodulation, which alters both cortical processing and pupil size. But pupil size is subject to a multitude of influences, whi...

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Main Authors: Jan W Brascamp, Gilles de Hollander, Michael D Wertheimer, Ashley N DePew, Tomas Knapen
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-08-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/66161
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author Jan W Brascamp
Gilles de Hollander
Michael D Wertheimer
Ashley N DePew
Tomas Knapen
author_facet Jan W Brascamp
Gilles de Hollander
Michael D Wertheimer
Ashley N DePew
Tomas Knapen
author_sort Jan W Brascamp
collection DOAJ
description The pupil provides a rich, non-invasive measure of the neural bases of perception and cognition and has been of particular value in uncovering the role of arousal-linked neuromodulation, which alters both cortical processing and pupil size. But pupil size is subject to a multitude of influences, which complicates unique interpretation. We measured pupils of observers experiencing perceptual multistability—an ever-changing subjective percept in the face of unchanging but inconclusive sensory input. In separate conditions, the endogenously generated perceptual changes were either task-relevant or not, allowing a separation between perception-related and task-related pupil signals. Perceptual changes were marked by a complex pupil response that could be decomposed into two components: a dilation tied to task execution and plausibly indicative of an arousal-linked noradrenaline surge, and an overlapping constriction tied to the perceptual transient and plausibly a marker of altered visual cortical representation. Constriction, but not dilation, amplitude systematically depended on the time interval between perceptual changes, possibly providing an overt index of neural adaptation. These results show that the pupil provides a simultaneous reading on interacting but dissociable neural processes during perceptual multistability, and suggest that arousal-linked neuromodulator release shapes action but not perception in these circumstances.
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spelling doaj.art-31d7701cea1347c7a34cc6b22d06da1b2022-12-22T04:32:37ZengeLife Sciences Publications LtdeLife2050-084X2021-08-011010.7554/eLife.66161Separable pupillary signatures of perception and action during perceptual multistabilityJan W Brascamp0https://orcid.org/0000-0001-7955-5479Gilles de Hollander1https://orcid.org/0000-0003-1988-5091Michael D Wertheimer2Ashley N DePew3https://orcid.org/0000-0002-8398-7319Tomas Knapen4https://orcid.org/0000-0001-5863-8689Michigan State University, Department of Psychology, East Lansing, United States; Michigan State University, Neuroscience Program, East Lansing, United StatesZurich Center for Neuroeconomics, Department of Economics, University of Zurich, Zurich, SwitzerlandMichigan State University, Department of Psychology, East Lansing, United StatesMichigan State University, Department of Psychology, East Lansing, United StatesVrije Universiteit Amsterdam, Amsterdam, Netherlands; Spinoza Centre for Neuroimaging, Royal Academy of Sciences, Amsterdam, NetherlandsThe pupil provides a rich, non-invasive measure of the neural bases of perception and cognition and has been of particular value in uncovering the role of arousal-linked neuromodulation, which alters both cortical processing and pupil size. But pupil size is subject to a multitude of influences, which complicates unique interpretation. We measured pupils of observers experiencing perceptual multistability—an ever-changing subjective percept in the face of unchanging but inconclusive sensory input. In separate conditions, the endogenously generated perceptual changes were either task-relevant or not, allowing a separation between perception-related and task-related pupil signals. Perceptual changes were marked by a complex pupil response that could be decomposed into two components: a dilation tied to task execution and plausibly indicative of an arousal-linked noradrenaline surge, and an overlapping constriction tied to the perceptual transient and plausibly a marker of altered visual cortical representation. Constriction, but not dilation, amplitude systematically depended on the time interval between perceptual changes, possibly providing an overt index of neural adaptation. These results show that the pupil provides a simultaneous reading on interacting but dissociable neural processes during perceptual multistability, and suggest that arousal-linked neuromodulator release shapes action but not perception in these circumstances.https://elifesciences.org/articles/66161visual perceptionpupilsnoradrenalinecognitive psychologymultistable perceptionbinocular rivalry
spellingShingle Jan W Brascamp
Gilles de Hollander
Michael D Wertheimer
Ashley N DePew
Tomas Knapen
Separable pupillary signatures of perception and action during perceptual multistability
eLife
visual perception
pupils
noradrenaline
cognitive psychology
multistable perception
binocular rivalry
title Separable pupillary signatures of perception and action during perceptual multistability
title_full Separable pupillary signatures of perception and action during perceptual multistability
title_fullStr Separable pupillary signatures of perception and action during perceptual multistability
title_full_unstemmed Separable pupillary signatures of perception and action during perceptual multistability
title_short Separable pupillary signatures of perception and action during perceptual multistability
title_sort separable pupillary signatures of perception and action during perceptual multistability
topic visual perception
pupils
noradrenaline
cognitive psychology
multistable perception
binocular rivalry
url https://elifesciences.org/articles/66161
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