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Sensory discrimination between innocuous and noxious cold by TRPM8-expressing DRG neurons of rats

The TRPM8 channel is a principal cold transducer that is expressed on some primary afferents of the somatic and cranial sensory systems. However, it is uncertain whether TRPM8-expressing afferent neurons have the ability to convey innocuous and noxious cold stimuli with sensory discrimination betwee...

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Autores principales: Sarria, Ignacio, Ling, Jennifer, Xu, Guang-Yin, Gu, Jianguo G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495675/
https://www.ncbi.nlm.nih.gov/pubmed/23092296
http://dx.doi.org/10.1186/1744-8069-8-79
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author Sarria, Ignacio
Ling, Jennifer
Xu, Guang-Yin
Gu, Jianguo G
author_facet Sarria, Ignacio
Ling, Jennifer
Xu, Guang-Yin
Gu, Jianguo G
author_sort Sarria, Ignacio
collection PubMed
description The TRPM8 channel is a principal cold transducer that is expressed on some primary afferents of the somatic and cranial sensory systems. However, it is uncertain whether TRPM8-expressing afferent neurons have the ability to convey innocuous and noxious cold stimuli with sensory discrimination between the two sub-modalities. Using rat dorsal root ganglion (DRG) neurons and the patch-clamp recording technique, we characterized membrane and action potential properties of TRPM8-expressing DRG neurons at 24°C and 10°C. TRPM8-expressing neurons could be classified into TTX-sensitive (TTXs/TRPM8) and TTX-resistant (TTXr/TRPM8) subtypes based on the sensitivity to tetrodotoxin (TTX) block of their action potentials. These two subtypes of cold-sensing cells displayed different membrane and action potential properties. Voltage-activated inward Na(+) currents were highly susceptible to cooling temperature and abolished by ~95% at 10°C in TTXs/TRPM8 DRG neurons, but remained substantially large at 10°C in TTXr/TRPM8 cells. In both TTXs/TRPM8 and TTXr/TRPM8 cells, voltage-activated outward K(+) currents were substantially inhibited at 10°C, and the cooling-sensitive outward currents resembled A-type K(+) currents. TTXs/TRPM8 neurons and TTXr/TRPM8 neurons were shown to fire action potentials at innocuous and noxious cold temperatures respectively, demonstrating sensory discrimination between innocuous and noxious cold by the two subpopulations of cold-sensing DRG neurons. The effects of cooling temperatures on voltage-gated Na(+) channels and A-type K(+) currents are likely to be contributing factors to sensory discrimination of cold by TTXs/TRPM8 and TTXr/TRPM8 afferent neurons.
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spelling pubmed-34956752012-11-13 Sensory discrimination between innocuous and noxious cold by TRPM8-expressing DRG neurons of rats Sarria, Ignacio Ling, Jennifer Xu, Guang-Yin Gu, Jianguo G Mol Pain Research The TRPM8 channel is a principal cold transducer that is expressed on some primary afferents of the somatic and cranial sensory systems. However, it is uncertain whether TRPM8-expressing afferent neurons have the ability to convey innocuous and noxious cold stimuli with sensory discrimination between the two sub-modalities. Using rat dorsal root ganglion (DRG) neurons and the patch-clamp recording technique, we characterized membrane and action potential properties of TRPM8-expressing DRG neurons at 24°C and 10°C. TRPM8-expressing neurons could be classified into TTX-sensitive (TTXs/TRPM8) and TTX-resistant (TTXr/TRPM8) subtypes based on the sensitivity to tetrodotoxin (TTX) block of their action potentials. These two subtypes of cold-sensing cells displayed different membrane and action potential properties. Voltage-activated inward Na(+) currents were highly susceptible to cooling temperature and abolished by ~95% at 10°C in TTXs/TRPM8 DRG neurons, but remained substantially large at 10°C in TTXr/TRPM8 cells. In both TTXs/TRPM8 and TTXr/TRPM8 cells, voltage-activated outward K(+) currents were substantially inhibited at 10°C, and the cooling-sensitive outward currents resembled A-type K(+) currents. TTXs/TRPM8 neurons and TTXr/TRPM8 neurons were shown to fire action potentials at innocuous and noxious cold temperatures respectively, demonstrating sensory discrimination between innocuous and noxious cold by the two subpopulations of cold-sensing DRG neurons. The effects of cooling temperatures on voltage-gated Na(+) channels and A-type K(+) currents are likely to be contributing factors to sensory discrimination of cold by TTXs/TRPM8 and TTXr/TRPM8 afferent neurons. BioMed Central 2012-10-24 /pmc/articles/PMC3495675/ /pubmed/23092296 http://dx.doi.org/10.1186/1744-8069-8-79 Text en Copyright ©2012 Sarria et al.; 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
Sarria, Ignacio
Ling, Jennifer
Xu, Guang-Yin
Gu, Jianguo G
Sensory discrimination between innocuous and noxious cold by TRPM8-expressing DRG neurons of rats
title Sensory discrimination between innocuous and noxious cold by TRPM8-expressing DRG neurons of rats
title_full Sensory discrimination between innocuous and noxious cold by TRPM8-expressing DRG neurons of rats
title_fullStr Sensory discrimination between innocuous and noxious cold by TRPM8-expressing DRG neurons of rats
title_full_unstemmed Sensory discrimination between innocuous and noxious cold by TRPM8-expressing DRG neurons of rats
title_short Sensory discrimination between innocuous and noxious cold by TRPM8-expressing DRG neurons of rats
title_sort sensory discrimination between innocuous and noxious cold by trpm8-expressing drg neurons of rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495675/
https://www.ncbi.nlm.nih.gov/pubmed/23092296
http://dx.doi.org/10.1186/1744-8069-8-79
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