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Characteristics of dorsal root ganglia neurons sensitive to Substance P
BACKGROUND: Substance P modulates ion channels and the excitability of sensory neurons in pain pathways. Within the heterogeneous population of Dorsal Root Ganglia (DRG) primary sensory neurons, the properties of cells that are sensitive to Substance P are poorly characterized. To define this popula...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280706/ https://www.ncbi.nlm.nih.gov/pubmed/25431155 http://dx.doi.org/10.1186/1744-8069-10-73 |
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author | Moraes, Eder Ricardo Kushmerick, Christopher Naves, Ligia Araujo |
author_facet | Moraes, Eder Ricardo Kushmerick, Christopher Naves, Ligia Araujo |
author_sort | Moraes, Eder Ricardo |
collection | PubMed |
description | BACKGROUND: Substance P modulates ion channels and the excitability of sensory neurons in pain pathways. Within the heterogeneous population of Dorsal Root Ganglia (DRG) primary sensory neurons, the properties of cells that are sensitive to Substance P are poorly characterized. To define this population better, dissociated rat DRG neurons were tested for their responsiveness to capsaicin, ATP and acid. Responses to ATP were classified according to the kinetics of current activation and desensitization. The same cells were then tested for modulation of action potential firing by Substance P. RESULTS: Acid and capsaicin currents were more frequently encountered in the largest diameter neurons. P2X3-like ATP currents were concentrated in small diameter neurons. Substance P modulated the excitability in 20 of 72 cells tested (28%). Of the Substance P sensitive cells, 10 exhibited an increase in excitability and 10 exhibited a decrease in excitability. There was no significant correlation between sensitivity to capsaicin and to Substance P. Excitatory effects of Substance P were strongly associated with cells that had large diameters, fired APs with large overshoots and slowly decaying after hyperpolarizations, and expressed acid currents at pH 7. No neurons that were excited by Substance P presented P2X3-like currents. In contrast, neurons that exhibited inhibitory effects of Substance P fired action potentials with rapidly decaying after hyperpolarizations. CONCLUSION: We conclude that excitatory effects of Substance P are restricted to a specific neuronal subpopulation with limited expression of putative nociceptive markers. |
format | Online Article Text |
id | pubmed-4280706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42807062015-01-01 Characteristics of dorsal root ganglia neurons sensitive to Substance P Moraes, Eder Ricardo Kushmerick, Christopher Naves, Ligia Araujo Mol Pain Research BACKGROUND: Substance P modulates ion channels and the excitability of sensory neurons in pain pathways. Within the heterogeneous population of Dorsal Root Ganglia (DRG) primary sensory neurons, the properties of cells that are sensitive to Substance P are poorly characterized. To define this population better, dissociated rat DRG neurons were tested for their responsiveness to capsaicin, ATP and acid. Responses to ATP were classified according to the kinetics of current activation and desensitization. The same cells were then tested for modulation of action potential firing by Substance P. RESULTS: Acid and capsaicin currents were more frequently encountered in the largest diameter neurons. P2X3-like ATP currents were concentrated in small diameter neurons. Substance P modulated the excitability in 20 of 72 cells tested (28%). Of the Substance P sensitive cells, 10 exhibited an increase in excitability and 10 exhibited a decrease in excitability. There was no significant correlation between sensitivity to capsaicin and to Substance P. Excitatory effects of Substance P were strongly associated with cells that had large diameters, fired APs with large overshoots and slowly decaying after hyperpolarizations, and expressed acid currents at pH 7. No neurons that were excited by Substance P presented P2X3-like currents. In contrast, neurons that exhibited inhibitory effects of Substance P fired action potentials with rapidly decaying after hyperpolarizations. CONCLUSION: We conclude that excitatory effects of Substance P are restricted to a specific neuronal subpopulation with limited expression of putative nociceptive markers. BioMed Central 2014-11-27 /pmc/articles/PMC4280706/ /pubmed/25431155 http://dx.doi.org/10.1186/1744-8069-10-73 Text en © Moraes et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 Moraes, Eder Ricardo Kushmerick, Christopher Naves, Ligia Araujo Characteristics of dorsal root ganglia neurons sensitive to Substance P |
title | Characteristics of dorsal root ganglia neurons sensitive to Substance P |
title_full | Characteristics of dorsal root ganglia neurons sensitive to Substance P |
title_fullStr | Characteristics of dorsal root ganglia neurons sensitive to Substance P |
title_full_unstemmed | Characteristics of dorsal root ganglia neurons sensitive to Substance P |
title_short | Characteristics of dorsal root ganglia neurons sensitive to Substance P |
title_sort | characteristics of dorsal root ganglia neurons sensitive to substance p |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280706/ https://www.ncbi.nlm.nih.gov/pubmed/25431155 http://dx.doi.org/10.1186/1744-8069-10-73 |
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