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Ion Channels Involved in Substance P-Mediated Nociception and Antinociception

Substance P (SP), an 11-amino-acid neuropeptide, has long been considered an effector of pain. However, accumulating studies have proposed a paradoxical role of SP in anti-nociception. Here, we review studies of SP-mediated nociception and anti-nociception in terms of peptide features, SP-modulated...

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Autores principales: Chang, Chu-Ting, Jiang, Bo-Yang, Chen, Chih-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479580/
https://www.ncbi.nlm.nih.gov/pubmed/30935032
http://dx.doi.org/10.3390/ijms20071596
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author Chang, Chu-Ting
Jiang, Bo-Yang
Chen, Chih-Cheng
author_facet Chang, Chu-Ting
Jiang, Bo-Yang
Chen, Chih-Cheng
author_sort Chang, Chu-Ting
collection PubMed
description Substance P (SP), an 11-amino-acid neuropeptide, has long been considered an effector of pain. However, accumulating studies have proposed a paradoxical role of SP in anti-nociception. Here, we review studies of SP-mediated nociception and anti-nociception in terms of peptide features, SP-modulated ion channels, and differential effector systems underlying neurokinin 1 receptors (NK1Rs) in differential cell types to elucidate the effect of SP and further our understanding of SP in anti-nociception. Most importantly, understanding the anti-nociceptive SP-NK1R pathway would provide new insights for analgesic drug development.
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spelling pubmed-64795802019-04-29 Ion Channels Involved in Substance P-Mediated Nociception and Antinociception Chang, Chu-Ting Jiang, Bo-Yang Chen, Chih-Cheng Int J Mol Sci Review Substance P (SP), an 11-amino-acid neuropeptide, has long been considered an effector of pain. However, accumulating studies have proposed a paradoxical role of SP in anti-nociception. Here, we review studies of SP-mediated nociception and anti-nociception in terms of peptide features, SP-modulated ion channels, and differential effector systems underlying neurokinin 1 receptors (NK1Rs) in differential cell types to elucidate the effect of SP and further our understanding of SP in anti-nociception. Most importantly, understanding the anti-nociceptive SP-NK1R pathway would provide new insights for analgesic drug development. MDPI 2019-03-30 /pmc/articles/PMC6479580/ /pubmed/30935032 http://dx.doi.org/10.3390/ijms20071596 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chang, Chu-Ting
Jiang, Bo-Yang
Chen, Chih-Cheng
Ion Channels Involved in Substance P-Mediated Nociception and Antinociception
title Ion Channels Involved in Substance P-Mediated Nociception and Antinociception
title_full Ion Channels Involved in Substance P-Mediated Nociception and Antinociception
title_fullStr Ion Channels Involved in Substance P-Mediated Nociception and Antinociception
title_full_unstemmed Ion Channels Involved in Substance P-Mediated Nociception and Antinociception
title_short Ion Channels Involved in Substance P-Mediated Nociception and Antinociception
title_sort ion channels involved in substance p-mediated nociception and antinociception
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479580/
https://www.ncbi.nlm.nih.gov/pubmed/30935032
http://dx.doi.org/10.3390/ijms20071596
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