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Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons
BACKGROUND: Superficial dorsal horn (SDH) neurons process nociceptive information and their excitability is partly determined by the properties of voltage-gated sodium channels. Recently, we showed the excitability and action potential properties of mouse SDH neurons change markedly during early pos...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381457/ https://www.ncbi.nlm.nih.gov/pubmed/25889748 http://dx.doi.org/10.1186/s12990-015-0014-5 |
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author | Tadros, Melissa A Farrell, Kristen E Graham, Brett A Brichta, Alan M Callister, Robert J |
author_facet | Tadros, Melissa A Farrell, Kristen E Graham, Brett A Brichta, Alan M Callister, Robert J |
author_sort | Tadros, Melissa A |
collection | PubMed |
description | BACKGROUND: Superficial dorsal horn (SDH) neurons process nociceptive information and their excitability is partly determined by the properties of voltage-gated sodium channels. Recently, we showed the excitability and action potential properties of mouse SDH neurons change markedly during early postnatal development. Here we compare sodium currents generated in neonate (P0-5) and young adult (≥P21) SDH neurons. RESULTS: Whole cell recordings were obtained from lumbar SDH neurons in transverse spinal cord slices (CsF internal, 32°C). Fast activating and inactivating TTX-sensitive inward currents were evoked by depolarization from a holding potential of −100 mV. Poorly clamped currents, based on a deflection in the IV relationship at potentials between −60 and −50 mV, were not accepted for analysis. Current density and decay time increased significantly between the first and third weeks of postnatal development, whereas time to peak was similar at both ages. This was accompanied by more subtle changes in activation range and steady state inactivation. Recovery from inactivation was slower and TTX-sensitivity was reduced in young adult neurons. CONCLUSIONS: Our study suggests sodium channel expression changes markedly during early postnatal development in mouse SDH neurons. The methods employed in this study can now be applied to future investigations of spinal cord sodium channel plasticity in murine pain models. |
format | Online Article Text |
id | pubmed-4381457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43814572015-04-02 Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons Tadros, Melissa A Farrell, Kristen E Graham, Brett A Brichta, Alan M Callister, Robert J Mol Pain Research BACKGROUND: Superficial dorsal horn (SDH) neurons process nociceptive information and their excitability is partly determined by the properties of voltage-gated sodium channels. Recently, we showed the excitability and action potential properties of mouse SDH neurons change markedly during early postnatal development. Here we compare sodium currents generated in neonate (P0-5) and young adult (≥P21) SDH neurons. RESULTS: Whole cell recordings were obtained from lumbar SDH neurons in transverse spinal cord slices (CsF internal, 32°C). Fast activating and inactivating TTX-sensitive inward currents were evoked by depolarization from a holding potential of −100 mV. Poorly clamped currents, based on a deflection in the IV relationship at potentials between −60 and −50 mV, were not accepted for analysis. Current density and decay time increased significantly between the first and third weeks of postnatal development, whereas time to peak was similar at both ages. This was accompanied by more subtle changes in activation range and steady state inactivation. Recovery from inactivation was slower and TTX-sensitivity was reduced in young adult neurons. CONCLUSIONS: Our study suggests sodium channel expression changes markedly during early postnatal development in mouse SDH neurons. The methods employed in this study can now be applied to future investigations of spinal cord sodium channel plasticity in murine pain models. BioMed Central 2015-03-28 /pmc/articles/PMC4381457/ /pubmed/25889748 http://dx.doi.org/10.1186/s12990-015-0014-5 Text en © Tadros et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tadros, Melissa A Farrell, Kristen E Graham, Brett A Brichta, Alan M Callister, Robert J Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons |
title | Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons |
title_full | Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons |
title_fullStr | Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons |
title_full_unstemmed | Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons |
title_short | Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons |
title_sort | properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381457/ https://www.ncbi.nlm.nih.gov/pubmed/25889748 http://dx.doi.org/10.1186/s12990-015-0014-5 |
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