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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3495675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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