Cargando…

Noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear Claudin-5 and Occludin

BACKGROUND: Noise exposure (NE) is a severe modern health hazard that induces hearing impairment. However, the noise-induced ultrastructural changes of blood-labyrinth barrier (BLB) and the potential involvements of tight junction proteins (TJP) remain inconclusive. We investigated the effects of NE...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Yong-Xiang, Zhu, Guo-Xia, Liu, Xin-Qin, Sun, Fei, Zhou, Ke, Wang, Shuang, Wang, Chun-Mei, Jia, Jin-Wen, Song, Jian-Tao, Lu, Lian-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299297/
https://www.ncbi.nlm.nih.gov/pubmed/25539640
http://dx.doi.org/10.1186/s12868-014-0136-0
_version_ 1782353374566416384
author Wu, Yong-Xiang
Zhu, Guo-Xia
Liu, Xin-Qin
Sun, Fei
Zhou, Ke
Wang, Shuang
Wang, Chun-Mei
Jia, Jin-Wen
Song, Jian-Tao
Lu, Lian-Jun
author_facet Wu, Yong-Xiang
Zhu, Guo-Xia
Liu, Xin-Qin
Sun, Fei
Zhou, Ke
Wang, Shuang
Wang, Chun-Mei
Jia, Jin-Wen
Song, Jian-Tao
Lu, Lian-Jun
author_sort Wu, Yong-Xiang
collection PubMed
description BACKGROUND: Noise exposure (NE) is a severe modern health hazard that induces hearing impairment. However, the noise-induced ultrastructural changes of blood-labyrinth barrier (BLB) and the potential involvements of tight junction proteins (TJP) remain inconclusive. We investigated the effects of NE on not only the ultrastructure of cochlea and permeability of BLB but also the expression of TJP within the guinea pig cochlea. RESULTS: Male albino guinea pigs were exposed to white noise for 4 h or 2 consecutive days (115 dB sound pressure level, 6 hours per day) and the hearing impairments and light microscopic change of BLB were evaluated with auditory brainstem responses (ABR) and the cochlear sensory epithelia surface preparation, respectively. The cochlear ultrastructure and BLB permeability after NE 2d were revealed with transmission electron microscope (TEM) and lanthanum nitrate-tracing techniques, respectively. The potential alterations of TJPs Claudin-5 and Occludin were quantified with immunohistochemistry and western blot. NE induced significant hearing impairment and NE 2d contributed to significant outer hair cell (OHC) loss that is most severe in the first row of outer hair cells. Furthermore, the loosen TJ and an obvious leakage of lanthanum nitrate particles beneath the basal lamina were revealed with TEM. Moreover, a dose-dependent decrease of Claudin-5 and Occludin was observed in the cochlea after NE. CONCLUSIONS: All these findings suggest that both decrease of Claudin-5 and Occludin and increased BLB permeability are involved in the pathologic process of noise-induced hearing impairment; however, the causal relationship and underlying mechanisms should be further investigated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12868-014-0136-0) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4299297
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-42992972015-01-21 Noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear Claudin-5 and Occludin Wu, Yong-Xiang Zhu, Guo-Xia Liu, Xin-Qin Sun, Fei Zhou, Ke Wang, Shuang Wang, Chun-Mei Jia, Jin-Wen Song, Jian-Tao Lu, Lian-Jun BMC Neurosci Research Article BACKGROUND: Noise exposure (NE) is a severe modern health hazard that induces hearing impairment. However, the noise-induced ultrastructural changes of blood-labyrinth barrier (BLB) and the potential involvements of tight junction proteins (TJP) remain inconclusive. We investigated the effects of NE on not only the ultrastructure of cochlea and permeability of BLB but also the expression of TJP within the guinea pig cochlea. RESULTS: Male albino guinea pigs were exposed to white noise for 4 h or 2 consecutive days (115 dB sound pressure level, 6 hours per day) and the hearing impairments and light microscopic change of BLB were evaluated with auditory brainstem responses (ABR) and the cochlear sensory epithelia surface preparation, respectively. The cochlear ultrastructure and BLB permeability after NE 2d were revealed with transmission electron microscope (TEM) and lanthanum nitrate-tracing techniques, respectively. The potential alterations of TJPs Claudin-5 and Occludin were quantified with immunohistochemistry and western blot. NE induced significant hearing impairment and NE 2d contributed to significant outer hair cell (OHC) loss that is most severe in the first row of outer hair cells. Furthermore, the loosen TJ and an obvious leakage of lanthanum nitrate particles beneath the basal lamina were revealed with TEM. Moreover, a dose-dependent decrease of Claudin-5 and Occludin was observed in the cochlea after NE. CONCLUSIONS: All these findings suggest that both decrease of Claudin-5 and Occludin and increased BLB permeability are involved in the pathologic process of noise-induced hearing impairment; however, the causal relationship and underlying mechanisms should be further investigated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12868-014-0136-0) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-24 /pmc/articles/PMC4299297/ /pubmed/25539640 http://dx.doi.org/10.1186/s12868-014-0136-0 Text en © Wu et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wu, Yong-Xiang
Zhu, Guo-Xia
Liu, Xin-Qin
Sun, Fei
Zhou, Ke
Wang, Shuang
Wang, Chun-Mei
Jia, Jin-Wen
Song, Jian-Tao
Lu, Lian-Jun
Noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear Claudin-5 and Occludin
title Noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear Claudin-5 and Occludin
title_full Noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear Claudin-5 and Occludin
title_fullStr Noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear Claudin-5 and Occludin
title_full_unstemmed Noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear Claudin-5 and Occludin
title_short Noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear Claudin-5 and Occludin
title_sort noise alters guinea pig’s blood-labyrinth barrier ultrastructure and permeability along with a decrease of cochlear claudin-5 and occludin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299297/
https://www.ncbi.nlm.nih.gov/pubmed/25539640
http://dx.doi.org/10.1186/s12868-014-0136-0
work_keys_str_mv AT wuyongxiang noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT zhuguoxia noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT liuxinqin noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT sunfei noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT zhouke noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT wangshuang noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT wangchunmei noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT jiajinwen noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT songjiantao noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin
AT lulianjun noisealtersguineapigsbloodlabyrinthbarrierultrastructureandpermeabilityalongwithadecreaseofcochlearclaudin5andoccludin