Cargando…

Untangling Perceptual Memory: Hysteresis and Adaptation Map into Separate Cortical Networks

Perception is an active inferential process in which prior knowledge is combined with sensory input, the result of which determines the contents of awareness. Accordingly, previous experience is known to help the brain “decide” what to perceive. However, a critical aspect that has not been addressed...

Descripción completa

Detalles Bibliográficos
Autores principales: Schwiedrzik, Caspar M., Ruff, Christian C., Lazar, Andreea, Leitner, Frauke C., Singer, Wolf, Melloni, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3977616/
https://www.ncbi.nlm.nih.gov/pubmed/23236204
http://dx.doi.org/10.1093/cercor/bhs396
_version_ 1782310448553525248
author Schwiedrzik, Caspar M.
Ruff, Christian C.
Lazar, Andreea
Leitner, Frauke C.
Singer, Wolf
Melloni, Lucia
author_facet Schwiedrzik, Caspar M.
Ruff, Christian C.
Lazar, Andreea
Leitner, Frauke C.
Singer, Wolf
Melloni, Lucia
author_sort Schwiedrzik, Caspar M.
collection PubMed
description Perception is an active inferential process in which prior knowledge is combined with sensory input, the result of which determines the contents of awareness. Accordingly, previous experience is known to help the brain “decide” what to perceive. However, a critical aspect that has not been addressed is that previous experience can exert 2 opposing effects on perception: An attractive effect, sensitizing the brain to perceive the same again (hysteresis), or a repulsive effect, making it more likely to perceive something else (adaptation). We used functional magnetic resonance imaging and modeling to elucidate how the brain entertains these 2 opposing processes, and what determines the direction of such experience-dependent perceptual effects. We found that although affecting our perception concurrently, hysteresis and adaptation map into distinct cortical networks: a widespread network of higher-order visual and fronto-parietal areas was involved in perceptual stabilization, while adaptation was confined to early visual areas. This areal and hierarchical segregation may explain how the brain maintains the balance between exploiting redundancies and staying sensitive to new information. We provide a Bayesian model that accounts for the coexistence of hysteresis and adaptation by separating their causes into 2 distinct terms: Hysteresis alters the prior, whereas adaptation changes the sensory evidence (the likelihood function).
format Online
Article
Text
id pubmed-3977616
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-39776162014-04-07 Untangling Perceptual Memory: Hysteresis and Adaptation Map into Separate Cortical Networks Schwiedrzik, Caspar M. Ruff, Christian C. Lazar, Andreea Leitner, Frauke C. Singer, Wolf Melloni, Lucia Cereb Cortex Articles Perception is an active inferential process in which prior knowledge is combined with sensory input, the result of which determines the contents of awareness. Accordingly, previous experience is known to help the brain “decide” what to perceive. However, a critical aspect that has not been addressed is that previous experience can exert 2 opposing effects on perception: An attractive effect, sensitizing the brain to perceive the same again (hysteresis), or a repulsive effect, making it more likely to perceive something else (adaptation). We used functional magnetic resonance imaging and modeling to elucidate how the brain entertains these 2 opposing processes, and what determines the direction of such experience-dependent perceptual effects. We found that although affecting our perception concurrently, hysteresis and adaptation map into distinct cortical networks: a widespread network of higher-order visual and fronto-parietal areas was involved in perceptual stabilization, while adaptation was confined to early visual areas. This areal and hierarchical segregation may explain how the brain maintains the balance between exploiting redundancies and staying sensitive to new information. We provide a Bayesian model that accounts for the coexistence of hysteresis and adaptation by separating their causes into 2 distinct terms: Hysteresis alters the prior, whereas adaptation changes the sensory evidence (the likelihood function). Oxford University Press 2014-05 2012-12-12 /pmc/articles/PMC3977616/ /pubmed/23236204 http://dx.doi.org/10.1093/cercor/bhs396 Text en © The Author 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.
spellingShingle Articles
Schwiedrzik, Caspar M.
Ruff, Christian C.
Lazar, Andreea
Leitner, Frauke C.
Singer, Wolf
Melloni, Lucia
Untangling Perceptual Memory: Hysteresis and Adaptation Map into Separate Cortical Networks
title Untangling Perceptual Memory: Hysteresis and Adaptation Map into Separate Cortical Networks
title_full Untangling Perceptual Memory: Hysteresis and Adaptation Map into Separate Cortical Networks
title_fullStr Untangling Perceptual Memory: Hysteresis and Adaptation Map into Separate Cortical Networks
title_full_unstemmed Untangling Perceptual Memory: Hysteresis and Adaptation Map into Separate Cortical Networks
title_short Untangling Perceptual Memory: Hysteresis and Adaptation Map into Separate Cortical Networks
title_sort untangling perceptual memory: hysteresis and adaptation map into separate cortical networks
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3977616/
https://www.ncbi.nlm.nih.gov/pubmed/23236204
http://dx.doi.org/10.1093/cercor/bhs396
work_keys_str_mv AT schwiedrzikcasparm untanglingperceptualmemoryhysteresisandadaptationmapintoseparatecorticalnetworks
AT ruffchristianc untanglingperceptualmemoryhysteresisandadaptationmapintoseparatecorticalnetworks
AT lazarandreea untanglingperceptualmemoryhysteresisandadaptationmapintoseparatecorticalnetworks
AT leitnerfraukec untanglingperceptualmemoryhysteresisandadaptationmapintoseparatecorticalnetworks
AT singerwolf untanglingperceptualmemoryhysteresisandadaptationmapintoseparatecorticalnetworks
AT mellonilucia untanglingperceptualmemoryhysteresisandadaptationmapintoseparatecorticalnetworks