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Support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment

Rodents use active whisker movements to explore their environment. The “slip hypothesis” of whisker-related tactile perception entails that short-lived kinematic events (abrupt whisker movements, called “slips”, due to bioelastic whisker properties that occur during active touch of textures) carry t...

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Autores principales: Waiblinger, Christian, Brugger, Dominik, Whitmire, Clarissa J., Stanley, Garrett B., Schwarz, Cornelius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4606012/
https://www.ncbi.nlm.nih.gov/pubmed/26528148
http://dx.doi.org/10.3389/fnint.2015.00053
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author Waiblinger, Christian
Brugger, Dominik
Whitmire, Clarissa J.
Stanley, Garrett B.
Schwarz, Cornelius
author_facet Waiblinger, Christian
Brugger, Dominik
Whitmire, Clarissa J.
Stanley, Garrett B.
Schwarz, Cornelius
author_sort Waiblinger, Christian
collection PubMed
description Rodents use active whisker movements to explore their environment. The “slip hypothesis” of whisker-related tactile perception entails that short-lived kinematic events (abrupt whisker movements, called “slips”, due to bioelastic whisker properties that occur during active touch of textures) carry the decisive texture information. Supporting this hypothesis, previous studies have shown that slip amplitude and frequency occur in a texture-dependent way. Further, experiments employing passive pulsatile whisker deflections revealed that perceptual performance based on pulse kinematics (i.e., signatures that resemble slips) is far superior to the one based on time-integrated variables like frequency and intensity. So far, pulsatile stimuli were employed in a noise free environment. However, the realistic scenario involves background noise (e.g., evoked by rubbing across the texture). Therefore, if slips are used for tactile perception, the tactile neuronal system would need to differentiate slip-evoked spikes from those evoked by noise. To test the animals under these more realistic conditions, we presented passive whisker-deflections to head-fixed trained rats, consisting of “slip-like” events (waveforms mimicking slips occurring with touch of real textures) embedded into background noise. Varying the (i) shapes (ramp or pulse); (ii) kinematics (amplitude, velocity, etc.); and (iii) the probabilities of occurrence of slip-like events, we observed that rats could readily detect slip-like events of different shapes against noisy background. Psychophysical curves revealed that the difference of slip event and noise amplitude determined perception, while increased probability of occurrence (frequency) had barely any effect. These results strongly support the notion that encoding of kinematics dominantly determines whisker-related tactile perception while the computation of frequency or intensity plays a minor role.
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spelling pubmed-46060122015-11-02 Support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment Waiblinger, Christian Brugger, Dominik Whitmire, Clarissa J. Stanley, Garrett B. Schwarz, Cornelius Front Integr Neurosci Neuroscience Rodents use active whisker movements to explore their environment. The “slip hypothesis” of whisker-related tactile perception entails that short-lived kinematic events (abrupt whisker movements, called “slips”, due to bioelastic whisker properties that occur during active touch of textures) carry the decisive texture information. Supporting this hypothesis, previous studies have shown that slip amplitude and frequency occur in a texture-dependent way. Further, experiments employing passive pulsatile whisker deflections revealed that perceptual performance based on pulse kinematics (i.e., signatures that resemble slips) is far superior to the one based on time-integrated variables like frequency and intensity. So far, pulsatile stimuli were employed in a noise free environment. However, the realistic scenario involves background noise (e.g., evoked by rubbing across the texture). Therefore, if slips are used for tactile perception, the tactile neuronal system would need to differentiate slip-evoked spikes from those evoked by noise. To test the animals under these more realistic conditions, we presented passive whisker-deflections to head-fixed trained rats, consisting of “slip-like” events (waveforms mimicking slips occurring with touch of real textures) embedded into background noise. Varying the (i) shapes (ramp or pulse); (ii) kinematics (amplitude, velocity, etc.); and (iii) the probabilities of occurrence of slip-like events, we observed that rats could readily detect slip-like events of different shapes against noisy background. Psychophysical curves revealed that the difference of slip event and noise amplitude determined perception, while increased probability of occurrence (frequency) had barely any effect. These results strongly support the notion that encoding of kinematics dominantly determines whisker-related tactile perception while the computation of frequency or intensity plays a minor role. Frontiers Media S.A. 2015-10-15 /pmc/articles/PMC4606012/ /pubmed/26528148 http://dx.doi.org/10.3389/fnint.2015.00053 Text en Copyright © 2015 Waiblinger, Brugger, Whitmire, Stanley and Schwarz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Waiblinger, Christian
Brugger, Dominik
Whitmire, Clarissa J.
Stanley, Garrett B.
Schwarz, Cornelius
Support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment
title Support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment
title_full Support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment
title_fullStr Support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment
title_full_unstemmed Support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment
title_short Support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment
title_sort support for the slip hypothesis from whisker-related tactile perception of rats in a noisy environment
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4606012/
https://www.ncbi.nlm.nih.gov/pubmed/26528148
http://dx.doi.org/10.3389/fnint.2015.00053
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