Literature DB >> 10575118

Age-related loss of distortion product otoacoustic emissions in four mouse strains.

A M Jimenez1, B B Stagner, G K Martin, B L Lonsbury-Martin.   

Abstract

Changes in cochlear function in four inbred strains of mice, CBA/CaJ (CBA), C57BL/6J (C57), BALB/cByJ (BALB), and WB/ReJ (WB), previously used to study age-related hearing loss, were evaluated serially as a function of age with 2f(1)-f(2) distortion-product otoacoustic emissions (DPOAEs). DPOAE levels in response to equilevel primary tones for geometric-mean (GM) frequencies from 5.6 to 48.5 kHz were recorded systematically as DP-grams and response/growth or input/output (I/O) functions at monthly intervals from about 2 to 15 months of age. Over the approximate 13-month measurement period, CBAs showed robust and unchanged DPOAEs for all tested frequencies, while BALBs, C57s, and WBs showed strain-specific, age-related decreases in DPOAEs that progressed systematically from the high to low frequencies. Specifically, for the youngest WBs at 2 months of age, no DPOAEs were recordable for GM frequencies > or = 32 kHz, while C57s and BALBs reached the identical stage of cochlear dysfunction by 5 and 8 months, respectively. The differential decline in DPOAE activity shown for WB, C57, and BALB mice supports the notion that they represent unique animal models of age-related changes in cochlear function. In contrast, the unchanging DPOAEs for CBAs over the same time period indicate that this strain makes an effective control for normal cochlear function in the mouse, at least, up to 15 months of age.

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Year:  1999        PMID: 10575118     DOI: 10.1016/s0378-5955(99)00154-9

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  29 in total

1.  Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain.

Authors:  Joseph R Latoche; Harold R Neely; Konrad Noben-Trauth
Journal:  Hear Res       Date:  2010-12-24       Impact factor: 3.208

2.  Assessing age-related ossification of the petro-occipital fissure: laying the foundation for understanding the clinicopathologies of the cranial base.

Authors:  Armand L Balboni; Thomas L Estenson; Joy S Reidenberg; Andrew D Bergemann; Jeffrey T Laitman
Journal:  Anat Rec A Discov Mol Cell Evol Biol       Date:  2005-01

3.  Auditory brainstem responses in 10 inbred strains of mice.

Authors:  Xiaoming Zhou; Philip H-S Jen; Kevin L Seburn; Wayne N Frankel; Qing Y Zheng
Journal:  Brain Res       Date:  2006-03-03       Impact factor: 3.252

4.  Selective hair cell ablation and noise exposure lead to different patterns of changes in the cochlea and the cochlear nucleus.

Authors:  Takaomi Kurioka; Min Young Lee; Amarins N Heeringa; Lisa A Beyer; Donald L Swiderski; Ariane C Kanicki; Lisa L Kabara; David F Dolan; Susan E Shore; Yehoash Raphael
Journal:  Neuroscience       Date:  2016-07-09       Impact factor: 3.590

5.  Gravity receptor aging in the CBA/CaJ strain: a comparison to auditory aging.

Authors:  Bruce Mock; Timothy A Jones; Sherri M Jones
Journal:  J Assoc Res Otolaryngol       Date:  2010-11-05

6.  Sex differences in distortion-product and transient-evoked otoacoustic emissions compared.

Authors:  Dennis McFadden; Glen K Martin; Barden B Stagner; Mindy M Maloney
Journal:  J Acoust Soc Am       Date:  2009-01       Impact factor: 1.840

Review 7.  Inheritance patterns of progressive hearing loss in laboratory strains of mice.

Authors:  Konrad Noben-Trauth; Kenneth R Johnson
Journal:  Brain Res       Date:  2009-02-21       Impact factor: 3.252

8.  Spatiotemporally controlled overexpression of cyclin D1 triggers generation of supernumerary cells in the postnatal mouse inner ear.

Authors:  Shikha Tarang; Umesh Pyakurel; Michael D Weston; Sarath Vijayakumar; Timothy Jones; Kay-Uwe Wagner; Sonia M Rocha-Sanchez
Journal:  Hear Res       Date:  2020-03-19       Impact factor: 3.208

9.  Otoconin-90 deletion leads to imbalance but normal hearing: a comparison with other otoconia mutants.

Authors:  X Zhao; S M Jones; E N Yamoah; Y Wang Lundberg
Journal:  Neuroscience       Date:  2008-02-10       Impact factor: 3.590

10.  A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction.

Authors:  Nahid G Robertson; Sherri M Jones; Theru A Sivakumaran; Anne B S Giersch; Sara A Jurado; Linda M Call; Constance E Miller; Stéphane F Maison; M Charles Liberman; Cynthia C Morton
Journal:  Hum Mol Genet       Date:  2008-08-12       Impact factor: 6.150

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