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Transforming growth factor β1 inhibition protects from noise-induced hearing loss
Excessive exposure to noise damages the principal cochlear structures leading to hearing impairment. Inflammatory and immune responses are central mechanisms in cochlear defensive response to noise but, if unregulated, they contribute to inner ear damage and hearing loss. Transforming growth factor...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367183/ https://www.ncbi.nlm.nih.gov/pubmed/25852546 http://dx.doi.org/10.3389/fnagi.2015.00032 |
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author | Murillo-Cuesta, Silvia Rodríguez-de la Rosa, Lourdes Contreras, Julio Celaya, Adelaida M. Camarero, Guadalupe Rivera, Teresa Varela-Nieto, Isabel |
author_facet | Murillo-Cuesta, Silvia Rodríguez-de la Rosa, Lourdes Contreras, Julio Celaya, Adelaida M. Camarero, Guadalupe Rivera, Teresa Varela-Nieto, Isabel |
author_sort | Murillo-Cuesta, Silvia |
collection | PubMed |
description | Excessive exposure to noise damages the principal cochlear structures leading to hearing impairment. Inflammatory and immune responses are central mechanisms in cochlear defensive response to noise but, if unregulated, they contribute to inner ear damage and hearing loss. Transforming growth factor β (TGF-β) is a key regulator of both responses and high levels of this factor have been associated with cochlear injury in hearing loss animal models. To evaluate the potential of targeting TGF-β as a therapeutic strategy for preventing or ameliorating noise-induced hearing loss (NIHL), we studied the auditory function, cochlear morphology, gene expression and oxidative stress markers in mice exposed to noise and treated with TGF-β1 peptidic inhibitors P17 and P144, just before or immediately after noise insult. Our results indicate that systemic administration of both peptides significantly improved both the evolution of hearing thresholds and the degenerative changes induced by noise-exposure in lateral wall structures. Moreover, treatments ameliorated the inflammatory state and redox balance. These therapeutic effects were dose-dependent and more effective if the TGF-β1 inhibitors were administered prior to inducing the injury. In conclusion, inhibition of TGF-β1 actions with antagonistic peptides represents a new, promising therapeutic strategy for the prevention and repair of noise-induced cochlear damage. |
format | Online Article Text |
id | pubmed-4367183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43671832015-04-07 Transforming growth factor β1 inhibition protects from noise-induced hearing loss Murillo-Cuesta, Silvia Rodríguez-de la Rosa, Lourdes Contreras, Julio Celaya, Adelaida M. Camarero, Guadalupe Rivera, Teresa Varela-Nieto, Isabel Front Aging Neurosci Neuroscience Excessive exposure to noise damages the principal cochlear structures leading to hearing impairment. Inflammatory and immune responses are central mechanisms in cochlear defensive response to noise but, if unregulated, they contribute to inner ear damage and hearing loss. Transforming growth factor β (TGF-β) is a key regulator of both responses and high levels of this factor have been associated with cochlear injury in hearing loss animal models. To evaluate the potential of targeting TGF-β as a therapeutic strategy for preventing or ameliorating noise-induced hearing loss (NIHL), we studied the auditory function, cochlear morphology, gene expression and oxidative stress markers in mice exposed to noise and treated with TGF-β1 peptidic inhibitors P17 and P144, just before or immediately after noise insult. Our results indicate that systemic administration of both peptides significantly improved both the evolution of hearing thresholds and the degenerative changes induced by noise-exposure in lateral wall structures. Moreover, treatments ameliorated the inflammatory state and redox balance. These therapeutic effects were dose-dependent and more effective if the TGF-β1 inhibitors were administered prior to inducing the injury. In conclusion, inhibition of TGF-β1 actions with antagonistic peptides represents a new, promising therapeutic strategy for the prevention and repair of noise-induced cochlear damage. Frontiers Media S.A. 2015-03-20 /pmc/articles/PMC4367183/ /pubmed/25852546 http://dx.doi.org/10.3389/fnagi.2015.00032 Text en Copyright © 2015 Murillo-Cuesta, Rodríguez-de la Rosa, Contreras, Celaya, Camarero, Rivera and Varela-Nieto. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Murillo-Cuesta, Silvia Rodríguez-de la Rosa, Lourdes Contreras, Julio Celaya, Adelaida M. Camarero, Guadalupe Rivera, Teresa Varela-Nieto, Isabel Transforming growth factor β1 inhibition protects from noise-induced hearing loss |
title | Transforming growth factor β1 inhibition protects from noise-induced hearing loss |
title_full | Transforming growth factor β1 inhibition protects from noise-induced hearing loss |
title_fullStr | Transforming growth factor β1 inhibition protects from noise-induced hearing loss |
title_full_unstemmed | Transforming growth factor β1 inhibition protects from noise-induced hearing loss |
title_short | Transforming growth factor β1 inhibition protects from noise-induced hearing loss |
title_sort | transforming growth factor β1 inhibition protects from noise-induced hearing loss |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367183/ https://www.ncbi.nlm.nih.gov/pubmed/25852546 http://dx.doi.org/10.3389/fnagi.2015.00032 |
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