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Decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system
Tactile information available to the rat vibrissal system begins as external forces that cause whisker deformations, which in turn excite mechanoreceptors in the follicle. Despite the fundamental mechanical origin of tactile information, primary sensory neurons in the trigeminal ganglion (Vg) have o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999311/ https://www.ncbi.nlm.nih.gov/pubmed/27348221 http://dx.doi.org/10.7554/eLife.13969 |
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author | Bush, Nicholas E Schroeder, Christopher L Hobbs, Jennifer A Yang, Anne ET Huet, Lucie A Solla, Sara A Hartmann, Mitra JZ |
author_facet | Bush, Nicholas E Schroeder, Christopher L Hobbs, Jennifer A Yang, Anne ET Huet, Lucie A Solla, Sara A Hartmann, Mitra JZ |
author_sort | Bush, Nicholas E |
collection | PubMed |
description | Tactile information available to the rat vibrissal system begins as external forces that cause whisker deformations, which in turn excite mechanoreceptors in the follicle. Despite the fundamental mechanical origin of tactile information, primary sensory neurons in the trigeminal ganglion (Vg) have often been described as encoding the kinematics (geometry) of object contact. Here we aimed to determine the extent to which Vg neurons encode the kinematics vs. mechanics of contact. We used models of whisker bending to quantify mechanical signals (forces and moments) at the whisker base while simultaneously monitoring whisker kinematics and recording single Vg units in both anesthetized rats and awake, body restrained rats. We employed a novel manual stimulation technique to deflect whiskers in a way that decouples kinematics from mechanics, and used Generalized Linear Models (GLMs) to show that Vg neurons more directly encode mechanical signals when the whisker is deflected in this decoupled stimulus space. DOI: http://dx.doi.org/10.7554/eLife.13969.001 |
format | Online Article Text |
id | pubmed-4999311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49993112016-08-29 Decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system Bush, Nicholas E Schroeder, Christopher L Hobbs, Jennifer A Yang, Anne ET Huet, Lucie A Solla, Sara A Hartmann, Mitra JZ eLife Computational and Systems Biology Tactile information available to the rat vibrissal system begins as external forces that cause whisker deformations, which in turn excite mechanoreceptors in the follicle. Despite the fundamental mechanical origin of tactile information, primary sensory neurons in the trigeminal ganglion (Vg) have often been described as encoding the kinematics (geometry) of object contact. Here we aimed to determine the extent to which Vg neurons encode the kinematics vs. mechanics of contact. We used models of whisker bending to quantify mechanical signals (forces and moments) at the whisker base while simultaneously monitoring whisker kinematics and recording single Vg units in both anesthetized rats and awake, body restrained rats. We employed a novel manual stimulation technique to deflect whiskers in a way that decouples kinematics from mechanics, and used Generalized Linear Models (GLMs) to show that Vg neurons more directly encode mechanical signals when the whisker is deflected in this decoupled stimulus space. DOI: http://dx.doi.org/10.7554/eLife.13969.001 eLife Sciences Publications, Ltd 2016-06-27 /pmc/articles/PMC4999311/ /pubmed/27348221 http://dx.doi.org/10.7554/eLife.13969 Text en © 2016, Bush et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Bush, Nicholas E Schroeder, Christopher L Hobbs, Jennifer A Yang, Anne ET Huet, Lucie A Solla, Sara A Hartmann, Mitra JZ Decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system |
title | Decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system |
title_full | Decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system |
title_fullStr | Decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system |
title_full_unstemmed | Decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system |
title_short | Decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system |
title_sort | decoupling kinematics and mechanics reveals coding properties of trigeminal ganglion neurons in the rat vibrissal system |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999311/ https://www.ncbi.nlm.nih.gov/pubmed/27348221 http://dx.doi.org/10.7554/eLife.13969 |
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