Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons

Voltage gated sodium channels (Na+ channels) play an important role in nociceptive transmission. They are intimately tied to the genesis and transmission of neuronal firing. Five different isoforms (Nav1.3, Nav1.6, Nav1.7, Nav1.8, and Nav1.9) have been linked to nociceptive responses. A change in th...

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Main Authors: Olivier eTheriault, Mohamed eChahine
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-09-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00285/full
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spelling doaj-6c7096a0898c45f6859c2998047bd3e62020-11-24T23:22:54ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022014-09-01810.3389/fncel.2014.00285110577Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neuronsOlivier eTheriault0Mohamed eChahine1Laval UniversityLaval UniversityVoltage gated sodium channels (Na+ channels) play an important role in nociceptive transmission. They are intimately tied to the genesis and transmission of neuronal firing. Five different isoforms (Nav1.3, Nav1.6, Nav1.7, Nav1.8, and Nav1.9) have been linked to nociceptive responses. A change in the biophysical properties of these channels or in their expression levels occurs in different pathological pain states. However, the precise involvement of the isoforms in the genesis and transmission of nociceptive responses is unknown. The aim of the present study was to investigate the synergy between the different populations Na+ channels that give individual neurons a unique electrophysical profile.We used the patch-clamp technique in the whole-cell configuration to record Na+ currents and action potentials from acutely dissociated small diameter DRG neurons (<30 µM) from adult rats. We also performed single cell qPCR on the same neurons. Our results revealed that there is a strong correlation between Na+ currents and mRNA transcripts in individual neurons. A cluster analysis showed that subgroups formed by Na+ channel transcripts by mRNA quantification have different biophysical properties. In addition, the firing frequency of the neurons was not affected by the relative populations of Na+ channel. The synergy between populations of Na+ channel in individual small diameter DRG neurons gives each neuron a unique electrophysiological profile. The Na+ channel remodeling that occurs in different pathological pain states may be responsible for the sensitization of the neurons.http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00285/fullPainNeuronal excitabilityvoltage-gated sodium channelbiophysical propertiesdorsal root ganglia neurons
collection DOAJ
language English
format Article
sources DOAJ
author Olivier eTheriault
Mohamed eChahine
spellingShingle Olivier eTheriault
Mohamed eChahine
Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons
Frontiers in Cellular Neuroscience
Pain
Neuronal excitability
voltage-gated sodium channel
biophysical properties
dorsal root ganglia neurons
author_facet Olivier eTheriault
Mohamed eChahine
author_sort Olivier eTheriault
title Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons
title_short Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons
title_full Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons
title_fullStr Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons
title_full_unstemmed Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons
title_sort correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2014-09-01
description Voltage gated sodium channels (Na+ channels) play an important role in nociceptive transmission. They are intimately tied to the genesis and transmission of neuronal firing. Five different isoforms (Nav1.3, Nav1.6, Nav1.7, Nav1.8, and Nav1.9) have been linked to nociceptive responses. A change in the biophysical properties of these channels or in their expression levels occurs in different pathological pain states. However, the precise involvement of the isoforms in the genesis and transmission of nociceptive responses is unknown. The aim of the present study was to investigate the synergy between the different populations Na+ channels that give individual neurons a unique electrophysical profile.We used the patch-clamp technique in the whole-cell configuration to record Na+ currents and action potentials from acutely dissociated small diameter DRG neurons (<30 µM) from adult rats. We also performed single cell qPCR on the same neurons. Our results revealed that there is a strong correlation between Na+ currents and mRNA transcripts in individual neurons. A cluster analysis showed that subgroups formed by Na+ channel transcripts by mRNA quantification have different biophysical properties. In addition, the firing frequency of the neurons was not affected by the relative populations of Na+ channel. The synergy between populations of Na+ channel in individual small diameter DRG neurons gives each neuron a unique electrophysiological profile. The Na+ channel remodeling that occurs in different pathological pain states may be responsible for the sensitization of the neurons.
topic Pain
Neuronal excitability
voltage-gated sodium channel
biophysical properties
dorsal root ganglia neurons
url http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00285/full
work_keys_str_mv AT olivieretheriault correlationoftheelectrophysiologicalprofilesandsodiumchanneltranscriptsofindividualratdorsalrootganglianeurons
AT mohamedechahine correlationoftheelectrophysiologicalprofilesandsodiumchanneltranscriptsofindividualratdorsalrootganglianeurons
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