Temporary reduction of distortion product otoacoustic emissions (DPOAEs) immediately following auditory brainstem response (ABR)

被引:10
作者
Mhatre, Anand N. [1 ,3 ]
Tajudeen, Bobby [1 ,2 ]
Welt, Elena M. [1 ,2 ]
Wartmann, Christopher [1 ,2 ]
Long, Glenis R. [5 ]
Lalwani, Anil K. [2 ,3 ,4 ]
机构
[1] NYU, Dept Otolaryngol, Sch Med, Mol Genet Lab, New York, NY 10016 USA
[2] NYU, Dept Otolaryngol, Sch Med, Lab Mol Otol, New York, NY 10016 USA
[3] NYU, Dept Physiol & Neurosci, Sch Med, New York, NY 10016 USA
[4] NYU, Dept Pediat, Sch Med, New York, NY 10016 USA
[5] CUNY, Grad Ctr, New York, NY 10016 USA
关键词
SUPEROXIDE-DISMUTASE; HEARING-LOSS; NOISE; MUTATIONS; OVEREXPRESSION; CADHERIN-23; SUSCEPTIBILITY; EXPOSURE; WALTZER; CDH23;
D O I
10.1016/j.heares.2010.06.012
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
The hearing status of an experimental animal is typically assessed in the laboratory setting by the combined use of auditory brainstem response (ABR) and distortion product otoacoustic emissions (DPOAEs), carried out in succession, with the former assay preceding the latter. This study reports a cautionary finding that the use of this accepted regimen yields a reduced DPOAE response. When the DPOAEs were performed after ABR testing, transient reduction of the DPOAE amplitudes was observed at all frequencies in both the inbred, C57/B6 and FVB/N, and the outbred, SW mouse strains. DPOAEs were reduced post-ABR in multiple mouse strains which suggests that this finding is not strain-specific but a general consequence of the preceding ABR analysis. The reduction in DPOAE was temporary: when re-tested at one hour, DPOAE amplitudes recovered to pre-ABR levels. In contrast to the ABR's impact on DPOAE response, ABR thresholds were not altered or reduced when preceded immediately by DPOAE measurements. The molecular alterations underlying the ABR-induced transient reduction of DPOAE remain to be determined. To investigate the potential role of reactive oxygen species in post-ABR DPOAE reduction, transgenic mice over-expressing SOD1, the cytoplasmic enzyme critical for removal of superoxide radicals were subjected to the same auditory testing regimen. Similar to their wild type littermates, the SOD1 transgenic mice also demonstrated post-ABR DPOAE reduction, and thus do not support a role for superoxide radicals in transient reduction of DPOAE. While toxic noise exposure is known to negatively impact OAE, transient decrease in DPOAE levels following standard ABR assay has not been previously described. A practical outcome from this study is a recommendation for reversal of the traditional order for carrying out auditory tests, with the OAE measurements preceding ABR assessment, thus ensuring that the DPOAE response is unaffected. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:180 / 185
页数:6
相关论文
共 29 条
[1]   Modification of otoacoustic emissions following ear-level exposure to MP3 player music [J].
Bhagat, Shaum P. ;
Davis, Anne M. .
INTERNATIONAL JOURNAL OF AUDIOLOGY, 2008, 47 (12) :751-760
[2]   Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 [J].
Bork, JM ;
Peters, LM ;
Riazuddin, S ;
Bernstein, SL ;
Ahmed, ZM ;
Ness, SL ;
Polomeno, R ;
Ramesh, A ;
Schloss, M ;
Srisailpathy, CRS ;
Wayne, S ;
Bellman, S ;
Desmukh, D ;
Ahmed, Z ;
Khan, SN ;
Kaloustian, VMD ;
Li, XC ;
Lalwani, A ;
Riazuddin, S ;
Bitner-Glindzicz, M ;
Nance, WE ;
Liu, XZ ;
Wistow, G ;
Smith, RJH ;
Griffith, AJ ;
Wilcox, ER ;
Friedman, TB ;
Morell, RJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (01) :26-37
[3]   A strategy for the ubiquitous overexpression of human catalase and CuZn superoxide dismutase genes in transgenic mice [J].
Chen, XL ;
Mele, J ;
Giese, H ;
Van Remmen, H ;
Dollé, MET ;
Steinhelper, M ;
Richardson, A ;
Vijg, J .
MECHANISMS OF AGEING AND DEVELOPMENT, 2003, 124 (02) :219-227
[4]   Effect of SOD1 overexpression on age- and noise-related hearing loss [J].
Coling, DE ;
Yu, KCY ;
Somand, D ;
Satar, B ;
Bai, U ;
Huang, TT ;
Seidman, MD ;
Epstein, CJ ;
Mhatre, AN ;
Lalwani, AK .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 34 (07) :873-880
[5]  
Desai Anjali, 1999, Noise Health, V1, P58
[6]   Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D [J].
Di Palma, F ;
Holme, RH ;
Bryda, EC ;
Belyantseva, IA ;
Pellegrino, R ;
Kachar, B ;
Steel, KP ;
Noben-Trauth, K .
NATURE GENETICS, 2001, 27 (01) :103-107
[7]   The role of oxidative stress in noise-induced hearing loss [J].
Henderson, D ;
Bielefeld, EC ;
Harris, KC ;
Hu, BH .
EAR AND HEARING, 2006, 27 (01) :1-19
[8]   Quantitative relationship of carboplatin dose to magnitude of inner and outer hair cell loss and the reduction in distortion product otoacoustic emission amplitude in chinchillas [J].
Hofstetter, P ;
Ding, DL ;
Powers, N ;
Salvi, RJ .
HEARING RESEARCH, 1997, 112 (1-2) :199-215
[9]   A major gene affecting age-related hearing loss in C57BL/6J mice [J].
Johnson, KR ;
Erway, LC ;
Cook, SA ;
Willott, JF ;
Zheng, QY .
HEARING RESEARCH, 1997, 114 (1-2) :83-92
[10]   A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice [J].
Johnson, KR ;
Zheng, QY ;
Erway, LC .
GENOMICS, 2000, 70 (02) :171-180