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Ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons

Sensory mechanical transduction – necessary for hearing, proprioception, and the senses of touch and pain – remains poorly understood. In somatosensation, even the basic properties of the mechanically sensitive excitatory ionic currents that are assumed to mediate mechanical transduction are largely...

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Detalles Bibliográficos
Autores principales: McCarter, Gordon C, Levine, Jon D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1563451/
https://www.ncbi.nlm.nih.gov/pubmed/16923187
http://dx.doi.org/10.1186/1744-8069-2-28
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author McCarter, Gordon C
Levine, Jon D
author_facet McCarter, Gordon C
Levine, Jon D
author_sort McCarter, Gordon C
collection PubMed
description Sensory mechanical transduction – necessary for hearing, proprioception, and the senses of touch and pain – remains poorly understood. In somatosensation, even the basic properties of the mechanically sensitive excitatory ionic currents that are assumed to mediate mechanical transduction are largely undescribed. We have recorded, from the soma of rat dorsal root ganglion (DRG) neurons in vitro, whole-cell ionic currents induced by the impact of a piezo-electrically driven glass probe. This transient mechanically activated current was observed in virtually all DRG neurons tested. In ion substitution experiments the current could be carried nonselectively by most cations, including divalent and organic cations, but not by chloride or sulfate ions. In addition, the mechanically activated current carried by monovalent cations was consistently blocked by millimolar concentrations of external calcium or magnesium. Based on these results, the transient mechanical transduction current observed in somatosensory neurons in vitro is mediated by large-pore mechanically gated channels nonselective for cations but impermeable to anions.
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spelling pubmed-15634512006-09-14 Ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons McCarter, Gordon C Levine, Jon D Mol Pain Research Sensory mechanical transduction – necessary for hearing, proprioception, and the senses of touch and pain – remains poorly understood. In somatosensation, even the basic properties of the mechanically sensitive excitatory ionic currents that are assumed to mediate mechanical transduction are largely undescribed. We have recorded, from the soma of rat dorsal root ganglion (DRG) neurons in vitro, whole-cell ionic currents induced by the impact of a piezo-electrically driven glass probe. This transient mechanically activated current was observed in virtually all DRG neurons tested. In ion substitution experiments the current could be carried nonselectively by most cations, including divalent and organic cations, but not by chloride or sulfate ions. In addition, the mechanically activated current carried by monovalent cations was consistently blocked by millimolar concentrations of external calcium or magnesium. Based on these results, the transient mechanical transduction current observed in somatosensory neurons in vitro is mediated by large-pore mechanically gated channels nonselective for cations but impermeable to anions. BioMed Central 2006-08-21 /pmc/articles/PMC1563451/ /pubmed/16923187 http://dx.doi.org/10.1186/1744-8069-2-28 Text en Copyright © 2006 McCarter and Levine; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
McCarter, Gordon C
Levine, Jon D
Ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons
title Ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons
title_full Ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons
title_fullStr Ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons
title_full_unstemmed Ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons
title_short Ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons
title_sort ionic basis of a mechanotransduction current in adult rat dorsal root ganglion neurons
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1563451/
https://www.ncbi.nlm.nih.gov/pubmed/16923187
http://dx.doi.org/10.1186/1744-8069-2-28
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