Literature DB >> 17997239

Comparison of distortion product otoacoustic emissions in 28 inbred strains of mice.

Glen K Martin1, Ana E Vazquez, Ana M Jimenez, Barden B Stagner, Mackenzie A Howard, Brenda L Lonsbury-Martin.   

Abstract

Cochlear function was evaluated in a longitudinal study of 28 inbred strains of mice at 3 and 5 mo of age using measures of distortion product otoacoustic emissions (DPOAEs) in response to a federal initiative to develop rapid mouse phenotyping methodologies. DP-grams at f(2) frequencies ranging from 6.3 to 54.2kHz were obtained in about 3min/ear by eliciting 2f(1)-f(2) DPOAEs in 0.1-octave steps of f(2) with primary tones at L(1)=L(2) =55, 65, and 75dB SPL. CBA/CaJ mice exhibited average levels of approximately 26dB SPL and this strain was selected as the normal reference strain against which the others were compared. Based upon the configurations of their DP-grams, the 28 mouse strains could be categorized into four distinct groups. That is, nine of the strains including the CBA were designated as the CBA-like group because these mice displayed robust DPOAE levels across frequency. In contrast, the remaining three groups all exhibited irregular DP-gram patterns. Specifically, eight of the remaining 19 strains showed a progressive high- to low-frequency reduction in DPOAE levels that was typical of age-related hearing loss (AHL) associated with mouse strains homozygous for the ahl allele and were labeled as AHL-like strains. Seven strains demonstrating relatively even patterns of reduced DPOAE levels across the frequency-test range were designated as Flat-loss strains. Finally, the remaining four strains exhibited no measurable DPOAEs at either 3 or 5 mo of age and thus were classified as Absent strains. Extending the f(2) test frequencies up to approximately 54kHz led to the detection of very early-onset reductions in cochlear function in non-CBA-like groups so that all strains could be categorized by 3 mo of age. Predictably, the AHL-like strains showed more pronounced DPOAE losses at 5 mo than at 3 mo. A similar deterioration in DPOAE levels was not apparent for the Flat-loss strains. Both the AHL-like and Flat-loss strains showed considerably more variability in DPOAE levels than did the CBA-like strains. Together, these findings indicate that DP-grams adequately reveal both frequency-specific loss patterns and details of inbred strain variability.

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Year:  2007        PMID: 17997239     DOI: 10.1016/j.heares.2007.09.002

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


  12 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.

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Journal:  Hear Res       Date:  2010-12-24       Impact factor: 3.208

2.  Deterioration of the Medial Olivocochlear Efferent System Accelerates Age-Related Hearing Loss in Pax2-Isl1 Transgenic Mice.

Authors:  Tetyana Chumak; Romana Bohuslavova; Iva Macova; Nicole Dodd; Daniela Buckiova; Bernd Fritzsch; Josef Syka; Gabriela Pavlinkova
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3.  A Chromosome 17 Locus Engenders Frequency-Specific Non-Progressive Hearing Loss that Contributes to Age-Related Hearing Loss in Mice.

Authors:  Braulio Peguero; Bruce L Tempel
Journal:  J Assoc Res Otolaryngol       Date:  2015-05-05

Review 4.  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

5.  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

6.  Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice.

Authors:  Konrad Noben-Trauth; Joseph R Latoche; Harold R Neely; Beth Bennett
Journal:  PLoS One       Date:  2010-07-07       Impact factor: 3.240

7.  Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation.

Authors:  Ruishuang Geng; Scott F Geller; Toshinori Hayashi; Catherine A Ray; Thomas A Reh; Olivia Bermingham-McDonogh; Sherri M Jones; Charles G Wright; Sami Melki; Yoshikazu Imanishi; Krzysztof Palczewski; Kumar N Alagramam; John G Flannery
Journal:  Hum Mol Genet       Date:  2009-05-03       Impact factor: 6.150

8.  FVB/NJ mice demonstrate a youthful sensitivity to noise-induced hearing loss and provide a useful genetic model for the study of neural hearing loss.

Authors:  Maria K Ho; Xin Li; Juemei Wang; Jeffrey D Ohmen; Rick A Friedman
Journal:  Audiol Neurotol Extra       Date:  2014-01-01

9.  Mitochondrial calcium uniporter is essential for hearing and hair cell preservation in congenic FVB/NJ mice.

Authors:  Mayakannan Manikandan; Steven Walker; Aditi R Deshmukh; Elizabeth Perea; Danqi Wang; Kumar N Alagramam; Ruben Stepanyan
Journal:  Sci Rep       Date:  2021-05-06       Impact factor: 4.379

10.  Genome-wide linkage analyses identify Hfhl1 and Hfhl3 with frequency-specific effects on the hearing spectrum of NIH Swiss mice.

Authors:  James M Keller; Konrad Noben-Trauth
Journal:  BMC Genet       Date:  2012-04-27       Impact factor: 2.797

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