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Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain

Chronic pain affects billions of lives globally and is a major public health problem in the United States. However, pain management is still a challenging task due to a lack of understanding of the fundamental mechanisms of pain. In the past decades transient receptor potential (TRP) channels have b...

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Detalles Bibliográficos
Autores principales: Luo, Jialie, Walters, Edgar T., Carlton, Susan M., Hu, Hongzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849790/
https://www.ncbi.nlm.nih.gov/pubmed/24396340
http://dx.doi.org/10.2174/1570159X113119990040
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author Luo, Jialie
Walters, Edgar T.
Carlton, Susan M.
Hu, Hongzhen
author_facet Luo, Jialie
Walters, Edgar T.
Carlton, Susan M.
Hu, Hongzhen
author_sort Luo, Jialie
collection PubMed
description Chronic pain affects billions of lives globally and is a major public health problem in the United States. However, pain management is still a challenging task due to a lack of understanding of the fundamental mechanisms of pain. In the past decades transient receptor potential (TRP) channels have been identified as molecular sensors of tissue damage and inflammation. Activation/sensitization of TRP channels in peripheral nociceptors produces neurogenic inflammation and contributes to both somatic and visceral pain. Pharmacological and genetic studies have affirmed the role of TRP channels in multiple forms of inflammatory and neuropathic pain. Thus pain-evoking TRP channels emerge as promising therapeutic targets for a wide variety of pain and inflammatory conditions
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spelling pubmed-38497902014-06-01 Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain Luo, Jialie Walters, Edgar T. Carlton, Susan M. Hu, Hongzhen Curr Neuropharmacol Article Chronic pain affects billions of lives globally and is a major public health problem in the United States. However, pain management is still a challenging task due to a lack of understanding of the fundamental mechanisms of pain. In the past decades transient receptor potential (TRP) channels have been identified as molecular sensors of tissue damage and inflammation. Activation/sensitization of TRP channels in peripheral nociceptors produces neurogenic inflammation and contributes to both somatic and visceral pain. Pharmacological and genetic studies have affirmed the role of TRP channels in multiple forms of inflammatory and neuropathic pain. Thus pain-evoking TRP channels emerge as promising therapeutic targets for a wide variety of pain and inflammatory conditions Bentham Science Publishers 2013-12 2013-12 /pmc/articles/PMC3849790/ /pubmed/24396340 http://dx.doi.org/10.2174/1570159X113119990040 Text en ©2013 Bentham Science Publishers http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Luo, Jialie
Walters, Edgar T.
Carlton, Susan M.
Hu, Hongzhen
Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain
title Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain
title_full Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain
title_fullStr Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain
title_full_unstemmed Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain
title_short Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain
title_sort targeting pain-evoking transient receptor potential channels for the treatment of pain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849790/
https://www.ncbi.nlm.nih.gov/pubmed/24396340
http://dx.doi.org/10.2174/1570159X113119990040
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