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Predictive whisker kinematics reveal context-dependent sensorimotor strategies

Animals actively move their sensory organs in order to acquire sensory information. Some rodents, such as mice and rats, employ cyclic scanning motions of their facial whiskers to explore their proximal surrounding, a behavior known as whisking. Here, we investigated the contingency of whisking kine...

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Autores principales: Wallach, Avner, Deutsch, David, Oram, Tess Baker, Ahissar, Ehud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274460/
https://www.ncbi.nlm.nih.gov/pubmed/32453721
http://dx.doi.org/10.1371/journal.pbio.3000571
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author Wallach, Avner
Deutsch, David
Oram, Tess Baker
Ahissar, Ehud
author_facet Wallach, Avner
Deutsch, David
Oram, Tess Baker
Ahissar, Ehud
author_sort Wallach, Avner
collection PubMed
description Animals actively move their sensory organs in order to acquire sensory information. Some rodents, such as mice and rats, employ cyclic scanning motions of their facial whiskers to explore their proximal surrounding, a behavior known as whisking. Here, we investigated the contingency of whisking kinematics on the animal’s behavioral context that arises from both internal processes (attention and expectations) and external constraints (available sensory and motor degrees of freedom). We recorded rat whisking at high temporal resolution in 2 experimental contexts—freely moving or head-fixed—and 2 spatial sensory configurations—a single row or 3 caudal whiskers on each side of the snout. We found that rapid sensorimotor twitches, called pumps, occurring during free-air whisking carry information about the rat’s upcoming exploratory direction, as demonstrated by the ability of these pumps to predict consequent head and body locomotion. Specifically, pump behavior during both voluntary motionlessness and imposed head fixation exposed a backward redistribution of sensorimotor exploratory resources. Further, head-fixed rats employed a wide range of whisking profiles to compensate for the loss of head- and body-motor degrees of freedom. Finally, changing the number of intact vibrissae available to a rat resulted in an alteration of whisking strategy consistent with the rat actively reallocating its remaining resources. In sum, this work shows that rats adapt their active exploratory behavior in a homeostatic attempt to preserve sensorimotor coverage under changing environmental conditions and changing sensory capacities, including those imposed by various laboratory conditions.
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spelling pubmed-72744602020-06-09 Predictive whisker kinematics reveal context-dependent sensorimotor strategies Wallach, Avner Deutsch, David Oram, Tess Baker Ahissar, Ehud PLoS Biol Research Article Animals actively move their sensory organs in order to acquire sensory information. Some rodents, such as mice and rats, employ cyclic scanning motions of their facial whiskers to explore their proximal surrounding, a behavior known as whisking. Here, we investigated the contingency of whisking kinematics on the animal’s behavioral context that arises from both internal processes (attention and expectations) and external constraints (available sensory and motor degrees of freedom). We recorded rat whisking at high temporal resolution in 2 experimental contexts—freely moving or head-fixed—and 2 spatial sensory configurations—a single row or 3 caudal whiskers on each side of the snout. We found that rapid sensorimotor twitches, called pumps, occurring during free-air whisking carry information about the rat’s upcoming exploratory direction, as demonstrated by the ability of these pumps to predict consequent head and body locomotion. Specifically, pump behavior during both voluntary motionlessness and imposed head fixation exposed a backward redistribution of sensorimotor exploratory resources. Further, head-fixed rats employed a wide range of whisking profiles to compensate for the loss of head- and body-motor degrees of freedom. Finally, changing the number of intact vibrissae available to a rat resulted in an alteration of whisking strategy consistent with the rat actively reallocating its remaining resources. In sum, this work shows that rats adapt their active exploratory behavior in a homeostatic attempt to preserve sensorimotor coverage under changing environmental conditions and changing sensory capacities, including those imposed by various laboratory conditions. Public Library of Science 2020-05-26 /pmc/articles/PMC7274460/ /pubmed/32453721 http://dx.doi.org/10.1371/journal.pbio.3000571 Text en © 2020 Wallach et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wallach, Avner
Deutsch, David
Oram, Tess Baker
Ahissar, Ehud
Predictive whisker kinematics reveal context-dependent sensorimotor strategies
title Predictive whisker kinematics reveal context-dependent sensorimotor strategies
title_full Predictive whisker kinematics reveal context-dependent sensorimotor strategies
title_fullStr Predictive whisker kinematics reveal context-dependent sensorimotor strategies
title_full_unstemmed Predictive whisker kinematics reveal context-dependent sensorimotor strategies
title_short Predictive whisker kinematics reveal context-dependent sensorimotor strategies
title_sort predictive whisker kinematics reveal context-dependent sensorimotor strategies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274460/
https://www.ncbi.nlm.nih.gov/pubmed/32453721
http://dx.doi.org/10.1371/journal.pbio.3000571
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