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Effects of Arousal on Mouse Sensory Cortex Depend on Modality

Changes in arousal modulate the activity of mouse sensory cortex, but studies in different mice and different sensory areas disagree on whether this modulation enhances or suppresses activity. We measured this modulation simultaneously in multiple cortical areas by imaging mice expressing voltage-se...

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Detalles Bibliográficos
Autores principales: Shimaoka, Daisuke, Harris, Kenneth D., Carandini, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883328/
https://www.ncbi.nlm.nih.gov/pubmed/29562173
http://dx.doi.org/10.1016/j.celrep.2018.02.092
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author Shimaoka, Daisuke
Harris, Kenneth D.
Carandini, Matteo
author_facet Shimaoka, Daisuke
Harris, Kenneth D.
Carandini, Matteo
author_sort Shimaoka, Daisuke
collection PubMed
description Changes in arousal modulate the activity of mouse sensory cortex, but studies in different mice and different sensory areas disagree on whether this modulation enhances or suppresses activity. We measured this modulation simultaneously in multiple cortical areas by imaging mice expressing voltage-sensitive fluorescent proteins (VSFP). VSFP imaging estimates local membrane potential across large portions of cortex. We used temporal filters to predict local potential from running speed or from pupil dilation, two measures of arousal. The filters provided good fits and revealed that the effects of arousal depend on modality. In the primary visual cortex (V1) and auditory cortex (Au), arousal caused depolarization followed by hyperpolarization. In the barrel cortex (S1b) and a secondary visual area (LM), it caused only hyperpolarization. In all areas, nonetheless, arousal reduced the phasic responses to trains of sensory stimuli. These results demonstrate diverse effects of arousal across sensory cortex but similar effects on sensory responses.
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spelling pubmed-58833282018-04-06 Effects of Arousal on Mouse Sensory Cortex Depend on Modality Shimaoka, Daisuke Harris, Kenneth D. Carandini, Matteo Cell Rep Article Changes in arousal modulate the activity of mouse sensory cortex, but studies in different mice and different sensory areas disagree on whether this modulation enhances or suppresses activity. We measured this modulation simultaneously in multiple cortical areas by imaging mice expressing voltage-sensitive fluorescent proteins (VSFP). VSFP imaging estimates local membrane potential across large portions of cortex. We used temporal filters to predict local potential from running speed or from pupil dilation, two measures of arousal. The filters provided good fits and revealed that the effects of arousal depend on modality. In the primary visual cortex (V1) and auditory cortex (Au), arousal caused depolarization followed by hyperpolarization. In the barrel cortex (S1b) and a secondary visual area (LM), it caused only hyperpolarization. In all areas, nonetheless, arousal reduced the phasic responses to trains of sensory stimuli. These results demonstrate diverse effects of arousal across sensory cortex but similar effects on sensory responses. Cell Press 2018-03-20 /pmc/articles/PMC5883328/ /pubmed/29562173 http://dx.doi.org/10.1016/j.celrep.2018.02.092 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shimaoka, Daisuke
Harris, Kenneth D.
Carandini, Matteo
Effects of Arousal on Mouse Sensory Cortex Depend on Modality
title Effects of Arousal on Mouse Sensory Cortex Depend on Modality
title_full Effects of Arousal on Mouse Sensory Cortex Depend on Modality
title_fullStr Effects of Arousal on Mouse Sensory Cortex Depend on Modality
title_full_unstemmed Effects of Arousal on Mouse Sensory Cortex Depend on Modality
title_short Effects of Arousal on Mouse Sensory Cortex Depend on Modality
title_sort effects of arousal on mouse sensory cortex depend on modality
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883328/
https://www.ncbi.nlm.nih.gov/pubmed/29562173
http://dx.doi.org/10.1016/j.celrep.2018.02.092
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