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Conveyance of texture signals along a rat whisker
Neuronal activities underlying a percept are constrained by the physics of sensory signals. In the tactile sense such constraints are frictional stick–slip events, occurring, amongst other vibrotactile features, when tactile sensors are in contact with objects. We reveal new biomechanical phenomena...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245408/ https://www.ncbi.nlm.nih.gov/pubmed/34193889 http://dx.doi.org/10.1038/s41598-021-92770-3 |
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author | Oladazimi, Maysam Putelat, Thibaut Szalai, Robert Noda, Kentaro Shimoyama, Isao Champneys, Alan Schwarz, Cornelius |
author_facet | Oladazimi, Maysam Putelat, Thibaut Szalai, Robert Noda, Kentaro Shimoyama, Isao Champneys, Alan Schwarz, Cornelius |
author_sort | Oladazimi, Maysam |
collection | PubMed |
description | Neuronal activities underlying a percept are constrained by the physics of sensory signals. In the tactile sense such constraints are frictional stick–slip events, occurring, amongst other vibrotactile features, when tactile sensors are in contact with objects. We reveal new biomechanical phenomena about the transmission of these microNewton forces at the tip of a rat’s whisker, where they occur, to the base where they engage primary afferents. Using high resolution videography and accurate measurement of axial and normal forces at the follicle, we show that the conical and curved rat whisker acts as a sign-converting amplification filter for moment to robustly engage primary afferents. Furthermore, we present a model based on geometrically nonlinear Cosserat rod theory and a friction model that recreates the observed whole-beam whisker dynamics. The model quantifies the relation between kinematics (positions and velocities) and dynamic variables (forces and moments). Thus, only videographic assessment of acceleration is required to estimate forces and moments measured by the primary afferents. Our study highlights how sensory systems deal with complex physical constraints of perceptual targets and sensors. |
format | Online Article Text |
id | pubmed-8245408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82454082021-07-06 Conveyance of texture signals along a rat whisker Oladazimi, Maysam Putelat, Thibaut Szalai, Robert Noda, Kentaro Shimoyama, Isao Champneys, Alan Schwarz, Cornelius Sci Rep Article Neuronal activities underlying a percept are constrained by the physics of sensory signals. In the tactile sense such constraints are frictional stick–slip events, occurring, amongst other vibrotactile features, when tactile sensors are in contact with objects. We reveal new biomechanical phenomena about the transmission of these microNewton forces at the tip of a rat’s whisker, where they occur, to the base where they engage primary afferents. Using high resolution videography and accurate measurement of axial and normal forces at the follicle, we show that the conical and curved rat whisker acts as a sign-converting amplification filter for moment to robustly engage primary afferents. Furthermore, we present a model based on geometrically nonlinear Cosserat rod theory and a friction model that recreates the observed whole-beam whisker dynamics. The model quantifies the relation between kinematics (positions and velocities) and dynamic variables (forces and moments). Thus, only videographic assessment of acceleration is required to estimate forces and moments measured by the primary afferents. Our study highlights how sensory systems deal with complex physical constraints of perceptual targets and sensors. Nature Publishing Group UK 2021-06-30 /pmc/articles/PMC8245408/ /pubmed/34193889 http://dx.doi.org/10.1038/s41598-021-92770-3 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Oladazimi, Maysam Putelat, Thibaut Szalai, Robert Noda, Kentaro Shimoyama, Isao Champneys, Alan Schwarz, Cornelius Conveyance of texture signals along a rat whisker |
title | Conveyance of texture signals along a rat whisker |
title_full | Conveyance of texture signals along a rat whisker |
title_fullStr | Conveyance of texture signals along a rat whisker |
title_full_unstemmed | Conveyance of texture signals along a rat whisker |
title_short | Conveyance of texture signals along a rat whisker |
title_sort | conveyance of texture signals along a rat whisker |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245408/ https://www.ncbi.nlm.nih.gov/pubmed/34193889 http://dx.doi.org/10.1038/s41598-021-92770-3 |
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