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Updated: Jul 18, 2026

Modified Experimental Conditions for Noise-Induced Hearing Loss in Mice and Assessment of Hearing Function and Outer Hair Cell Damage
Published on: February 10, 2023
Genetic dependence of cochlear cells and structures injured by noise
Kevin K Ohlemiller1, Patricia M Gagnon
1Department of Otolaryngology, Washington University School of Medicine, 660 S. Euclid, St. Louis, MO 63110, United States. kohlemiller@wustl.edu
Abstract:
The acute and permanent effects of a single damaging noise exposure were compared in CBA/J, C57BL/6 (B6), and closely related strains of mice. Two hours of broadband noise (4-45 kHz) at 110 dB SPL led to temporary reduction in the endocochlear potential (EP) of CBA/J and CBA/CaJ (CBA) mice and acute cellular changes in cochlear stria vascularis and spiral ligament. For the same exposure, B6 mice showed no EP reduction and little of the pathology seen in CBA. Eight weeks after exposure, all mice showed a normal EP, but only CBA mice showed injury and cell loss in cochlear lateral wall, despite the fact that B6 sustained larger permanent threshold shifts. Examination of noise injury in B6 congenics carrying alternate alleles of genes encoding otocadherin (Cdh23), agouti protein, and tyrosinase (albinism) indicated that none of these loci can account for the strain differences observed. Examination of CBA x B6 F1 mice and N2 backcross mice to B6 further indicated that susceptibility to noise-related EP reduction and associated cell pathology are inherited in an autosomal dominant manner, and are established by one or a few large effect quantitative trait loci. Findings support a common genetic basis for an entire constellation of noise-related cochlear pathologies in cochlear lateral wall and spiral limbus. Even within species, cellular targets of acute and permanent cochlear noise injury may vary with genetic makeup.
Insights
Genetic differences in mice influence susceptibility to noise-induced hearing loss. CBA mice show more cochlear damage than B6 mice after noise exposure, indicating a genetic basis for hearing injury.
Area of Science:
- Ototoxicology
- Auditory Neuroscience
- Genetics of Hearing
Background:
- Noise-induced hearing loss is a significant health concern.
- Genetic factors play a role in individual susceptibility to noise damage.
- Understanding these genetic factors is crucial for developing targeted protective strategies.
Purpose of the Study:
- To compare the acute and permanent effects of noise exposure in different mouse strains.
- To identify genetic loci responsible for strain-dependent differences in noise susceptibility.
- To elucidate the inheritance patterns of noise-induced cochlear pathology.
Main Methods:
- Exposure of CBA/J and C57BL/6 (B6) mice to broadband noise (110 dB SPL for 2 hours).
- Assessment of endocochlear potential (EP) and cochlear pathology (stria vascularis, spiral ligament, lateral wall).
- Genetic analysis using congenic strains, F1 hybrids, and N2 backcross mice.
Main Results:
- CBA mice exhibited temporary EP reduction and acute cellular changes, while B6 mice showed minimal effects.
- Permanent threshold shifts were larger in B6 mice, but CBA mice displayed cochlear injury and cell loss.
- Susceptibility to noise-induced EP reduction and pathology is inherited in an autosomal dominant manner, linked to a few large-effect quantitative trait loci.
Conclusions:
- Genetic makeup significantly influences the acute and permanent effects of noise exposure on the cochlea.
- A common genetic basis underlies various noise-related cochlear pathologies.
- Cellular targets of noise injury can differ based on genetic background, even within the same species.
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