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Role of the transient receptor potential vanilloid 1 in inflammation and sepsis
The transient receptor potential vanilloid 1 (TRPV1) is a thermoreceptor that responds to noxious temperatures, as well as to chemical agonists, such as vanilloids and protons. In addition, its channel activity is notably potentiated by proinflammatory mediators released upon tissue damage. The TRPV...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218746/ https://www.ncbi.nlm.nih.gov/pubmed/22096371 http://dx.doi.org/10.2147/JIR.S12978 |
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author | Devesa, Isabel Planells-Cases, Rosa Fernández-Ballester, Gregorio González-Ros, José Manuel Ferrer-Montiel, Antonio Fernández-Carvajal, Asia |
author_facet | Devesa, Isabel Planells-Cases, Rosa Fernández-Ballester, Gregorio González-Ros, José Manuel Ferrer-Montiel, Antonio Fernández-Carvajal, Asia |
author_sort | Devesa, Isabel |
collection | PubMed |
description | The transient receptor potential vanilloid 1 (TRPV1) is a thermoreceptor that responds to noxious temperatures, as well as to chemical agonists, such as vanilloids and protons. In addition, its channel activity is notably potentiated by proinflammatory mediators released upon tissue damage. The TRPV1 contribution to sensory neuron sensitization by proalgesic agents has signaled this receptor as a prime target for analgesic and anti-inflammatory drug intervention. However, TRPV1 antagonists have notably failed in clinical and preclinical studies because of their unwanted side effects. Recent reports have unveiled previously unrecognized anti-inflammatory and protective functions of TRPV1 in several diseases. For instance, this channel has been suggested to play an anti-inflammatory role in sepsis. Therefore, the use of potent TRPV1 antagonists as a general strategy to treat inflammation must be cautiously considered, given the deleterious effects that may arise from inhibiting the population of channels that have a protective function. The use of TRPV1 antagonists may be limited to treating those pathologies where enhanced receptor activity contributes to the inflamed state. Alternatively, therapeutic paradigms, such as reduction of inflammatory-mediated increase of receptor expression in the cell surface, may be a better strategy to prevent abrogation of the TRPV1 subpopulation involved in anti-inflammatory and protective processes. |
format | Online Article Text |
id | pubmed-3218746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32187462011-11-17 Role of the transient receptor potential vanilloid 1 in inflammation and sepsis Devesa, Isabel Planells-Cases, Rosa Fernández-Ballester, Gregorio González-Ros, José Manuel Ferrer-Montiel, Antonio Fernández-Carvajal, Asia J Inflamm Res Review The transient receptor potential vanilloid 1 (TRPV1) is a thermoreceptor that responds to noxious temperatures, as well as to chemical agonists, such as vanilloids and protons. In addition, its channel activity is notably potentiated by proinflammatory mediators released upon tissue damage. The TRPV1 contribution to sensory neuron sensitization by proalgesic agents has signaled this receptor as a prime target for analgesic and anti-inflammatory drug intervention. However, TRPV1 antagonists have notably failed in clinical and preclinical studies because of their unwanted side effects. Recent reports have unveiled previously unrecognized anti-inflammatory and protective functions of TRPV1 in several diseases. For instance, this channel has been suggested to play an anti-inflammatory role in sepsis. Therefore, the use of potent TRPV1 antagonists as a general strategy to treat inflammation must be cautiously considered, given the deleterious effects that may arise from inhibiting the population of channels that have a protective function. The use of TRPV1 antagonists may be limited to treating those pathologies where enhanced receptor activity contributes to the inflamed state. Alternatively, therapeutic paradigms, such as reduction of inflammatory-mediated increase of receptor expression in the cell surface, may be a better strategy to prevent abrogation of the TRPV1 subpopulation involved in anti-inflammatory and protective processes. Dove Medical Press 2011-05-24 /pmc/articles/PMC3218746/ /pubmed/22096371 http://dx.doi.org/10.2147/JIR.S12978 Text en © 2011 Devesa et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Review Devesa, Isabel Planells-Cases, Rosa Fernández-Ballester, Gregorio González-Ros, José Manuel Ferrer-Montiel, Antonio Fernández-Carvajal, Asia Role of the transient receptor potential vanilloid 1 in inflammation and sepsis |
title | Role of the transient receptor potential vanilloid 1 in inflammation and sepsis |
title_full | Role of the transient receptor potential vanilloid 1 in inflammation and sepsis |
title_fullStr | Role of the transient receptor potential vanilloid 1 in inflammation and sepsis |
title_full_unstemmed | Role of the transient receptor potential vanilloid 1 in inflammation and sepsis |
title_short | Role of the transient receptor potential vanilloid 1 in inflammation and sepsis |
title_sort | role of the transient receptor potential vanilloid 1 in inflammation and sepsis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218746/ https://www.ncbi.nlm.nih.gov/pubmed/22096371 http://dx.doi.org/10.2147/JIR.S12978 |
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