Exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in rats

The ears are air-filled structures that are directly impacted during blast exposure. In addition to hearing loss and tinnitus, blast victims often complain of vertigo, dizziness and unsteady posture, suggesting that blast exposure induces damage to the vestibular end organs in the inner ear. However...

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Published in:Journal of Otology
Main Authors: Yue Yu, Jun Huang, Xuehui Tang, Jerome Allison, David Sandlin, Dalian Ding, Yi Pang, Chunming Zhang, Tianwen Chen, Nathan Yin, Lan Chen, William Mustain, Wu Zhou, Hong Zhu
Format: Article
Language:English
Published: Tsinghua University Press 2020-09-01
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1672293019301333
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author Yue Yu
Jun Huang
Xuehui Tang
Jerome Allison
David Sandlin
Dalian Ding
Yi Pang
Chunming Zhang
Tianwen Chen
Nathan Yin
Lan Chen
William Mustain
Wu Zhou
Hong Zhu
author_facet Yue Yu
Jun Huang
Xuehui Tang
Jerome Allison
David Sandlin
Dalian Ding
Yi Pang
Chunming Zhang
Tianwen Chen
Nathan Yin
Lan Chen
William Mustain
Wu Zhou
Hong Zhu
author_sort Yue Yu
collection DOAJ
container_title Journal of Otology
description The ears are air-filled structures that are directly impacted during blast exposure. In addition to hearing loss and tinnitus, blast victims often complain of vertigo, dizziness and unsteady posture, suggesting that blast exposure induces damage to the vestibular end organs in the inner ear. However, the underlying mechanisms remain to be elucidated. In this report, single vestibular afferent activity and the vestibulo-ocular reflex (VOR) were investigated before and after exposure to blast shock waves (∼20 PSI) delivered into the left external ear canals of anesthetized rats. Single vestibular afferent activity was recorded from the superior branch of the left vestibular nerves of the blast-treated and control rats one day after blast exposure. Blast exposure reduced the spontaneous discharge rates of the otolith and canal afferents. Blast exposure also reduced the sensitivity of irregular canal afferents to sinusoidal head rotation at 0.5–2Hz. Blast exposure, however, resulted in few changes in the VOR responses to sinusoidal head rotation and translation. To the best of our knowledge, this is the first study that reports blast exposure-induced damage to vestibular afferents in an animal model. These results provide insights that may be helpful in developing biomarkers for early diagnosis of blast-induced vestibular deficits in military and civilian populations.
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spelling doaj-e613b383ba254381bfd9ceb5e09eea0e2025-11-03T00:45:10ZengTsinghua University PressJournal of Otology1672-29302020-09-01153778510.1016/j.joto.2020.01.003Exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in ratsYue Yu0Jun Huang1Xuehui Tang2Jerome Allison3David Sandlin4Dalian Ding5Yi Pang6Chunming Zhang7Tianwen Chen8Nathan Yin9Lan Chen10William Mustain11Wu Zhou12Hong Zhu13Departmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USADepartmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USADepartmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USADepartmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USA; Department of Neurobiology and Anatomical Sciences, University of Mississippi Medical Center, Jackson, MS, USAProgram in Neuroscience, University of Mississippi Medical Center, Jackson, MS, USACenter for Hearing and Deafness, University at Buffalo, Buffalo, NY, USADepartment of Pediatric, University of Mississippi Medical Center, Jackson, MS, USADepartment of Otolaryngology, First Affiliated Hospital, Shanxi Medical University, Taiyuan Shanxi, 030001, ChinaDepartmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USADepartmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USADepartmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USADepartmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USADepartmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USA; Department of Neurobiology and Anatomical Sciences, University of Mississippi Medical Center, Jackson, MS, USA; Department of Neurology, University of Mississippi Medical Center, Jackson, MS, USA; Corresponding author. Department of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS, 39216, USA.Departmant of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, Jackson, MS, USA; Department of Neurobiology and Anatomical Sciences, University of Mississippi Medical Center, Jackson, MS, USA; Corresponding author. Department of Otolaryngology and Communicative Sciences, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS, 39216, USA.The ears are air-filled structures that are directly impacted during blast exposure. In addition to hearing loss and tinnitus, blast victims often complain of vertigo, dizziness and unsteady posture, suggesting that blast exposure induces damage to the vestibular end organs in the inner ear. However, the underlying mechanisms remain to be elucidated. In this report, single vestibular afferent activity and the vestibulo-ocular reflex (VOR) were investigated before and after exposure to blast shock waves (∼20 PSI) delivered into the left external ear canals of anesthetized rats. Single vestibular afferent activity was recorded from the superior branch of the left vestibular nerves of the blast-treated and control rats one day after blast exposure. Blast exposure reduced the spontaneous discharge rates of the otolith and canal afferents. Blast exposure also reduced the sensitivity of irregular canal afferents to sinusoidal head rotation at 0.5–2Hz. Blast exposure, however, resulted in few changes in the VOR responses to sinusoidal head rotation and translation. To the best of our knowledge, this is the first study that reports blast exposure-induced damage to vestibular afferents in an animal model. These results provide insights that may be helpful in developing biomarkers for early diagnosis of blast-induced vestibular deficits in military and civilian populations.http://www.sciencedirect.com/science/article/pii/S1672293019301333Primary blast injuryVestibular end organVestibulo-ocular reflexVestibular afferentVestibular hair cell
spellingShingle Yue Yu
Jun Huang
Xuehui Tang
Jerome Allison
David Sandlin
Dalian Ding
Yi Pang
Chunming Zhang
Tianwen Chen
Nathan Yin
Lan Chen
William Mustain
Wu Zhou
Hong Zhu
Exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in rats
Primary blast injury
Vestibular end organ
Vestibulo-ocular reflex
Vestibular afferent
Vestibular hair cell
title Exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in rats
title_full Exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in rats
title_fullStr Exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in rats
title_full_unstemmed Exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in rats
title_short Exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in rats
title_sort exposure to blast shock waves via the ear canal induces deficits in vestibular afferent function in rats
topic Primary blast injury
Vestibular end organ
Vestibulo-ocular reflex
Vestibular afferent
Vestibular hair cell
url http://www.sciencedirect.com/science/article/pii/S1672293019301333
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