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Non-Analgesic Symptomatic or Disease—Modifying Potential of TRPA1

TRPA1, a versatile ion channel of the Transient Receptor Potential (TRP) channel family, detects a large variety of chemicals and can contribute to signal processing of other stimuli, e.g., due to its sensitivity to cytosolic calcium elevation or phosphoinositolphosphate modulation. At first, TRPA1...

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Detalles Bibliográficos
Autores principales: Heber, Stefan, Fischer, Michael J.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836032/
https://www.ncbi.nlm.nih.gov/pubmed/31547502
http://dx.doi.org/10.3390/medsci7100099
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author Heber, Stefan
Fischer, Michael J.M.
author_facet Heber, Stefan
Fischer, Michael J.M.
author_sort Heber, Stefan
collection PubMed
description TRPA1, a versatile ion channel of the Transient Receptor Potential (TRP) channel family, detects a large variety of chemicals and can contribute to signal processing of other stimuli, e.g., due to its sensitivity to cytosolic calcium elevation or phosphoinositolphosphate modulation. At first, TRPA1 was found on sensory neurons, where it can act as a sensor for potential or actual tissue damage that ultimately may elicit pain or itch as warning symptoms. This review provides an update regarding the analgesic and antipruritic potential of TRPA1 modulation and the respective clinical trials. Furthermore, TRPA1 has been found in an increasing amount of other cell types. Therefore, the main focus of the review is to discuss the non-analgesic and particularly the disease-modifying potential of TRPA1. This includes diseases of the respiratory system, cancer, ischemia, allergy, diabetes, and the gastrointestinal system. The involvement of TRPA1 in the respective pathophysiological cascades is so far mainly based on pre-clinical data.
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spelling pubmed-68360322019-11-25 Non-Analgesic Symptomatic or Disease—Modifying Potential of TRPA1 Heber, Stefan Fischer, Michael J.M. Med Sci (Basel) Review TRPA1, a versatile ion channel of the Transient Receptor Potential (TRP) channel family, detects a large variety of chemicals and can contribute to signal processing of other stimuli, e.g., due to its sensitivity to cytosolic calcium elevation or phosphoinositolphosphate modulation. At first, TRPA1 was found on sensory neurons, where it can act as a sensor for potential or actual tissue damage that ultimately may elicit pain or itch as warning symptoms. This review provides an update regarding the analgesic and antipruritic potential of TRPA1 modulation and the respective clinical trials. Furthermore, TRPA1 has been found in an increasing amount of other cell types. Therefore, the main focus of the review is to discuss the non-analgesic and particularly the disease-modifying potential of TRPA1. This includes diseases of the respiratory system, cancer, ischemia, allergy, diabetes, and the gastrointestinal system. The involvement of TRPA1 in the respective pathophysiological cascades is so far mainly based on pre-clinical data. MDPI 2019-09-23 /pmc/articles/PMC6836032/ /pubmed/31547502 http://dx.doi.org/10.3390/medsci7100099 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
Heber, Stefan
Fischer, Michael J.M.
Non-Analgesic Symptomatic or Disease—Modifying Potential of TRPA1
title Non-Analgesic Symptomatic or Disease—Modifying Potential of TRPA1
title_full Non-Analgesic Symptomatic or Disease—Modifying Potential of TRPA1
title_fullStr Non-Analgesic Symptomatic or Disease—Modifying Potential of TRPA1
title_full_unstemmed Non-Analgesic Symptomatic or Disease—Modifying Potential of TRPA1
title_short Non-Analgesic Symptomatic or Disease—Modifying Potential of TRPA1
title_sort non-analgesic symptomatic or disease—modifying potential of trpa1
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836032/
https://www.ncbi.nlm.nih.gov/pubmed/31547502
http://dx.doi.org/10.3390/medsci7100099
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