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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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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. |
format | Online Article Text |
id | pubmed-4606012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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