Age-related hearing impairment in senescence-accelerated mouse (SAM). 1994

Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
Department of Otolaryngology, Kyoto Prefectural University of Medicine, Japan.

The auditory brainstem response and histopathology of the cochlea were investigated in an accelerated senescence-prone strain, SAM-P/1 mice and a senescence-resistant strain, SAM-R/1 mice. Each strain displayed an age-related auditory loss expressed as elevated thresholds similar to human hearing loss in that high-frequency losses occurred earlier than middle- or low-frequency losses. SAM-P/1 showed a more rapid decline of hearing with age than did SAM-R/1. Interpeak intervals I-III and I-IV were prolonged with age in both strains, especially at high frequency. The prolongation was more marked in SAM-P/1 than in SAM-R/1. The decrease in amplitude of wave I observed in both strains was greater in SAM-P/1 than in SAM-R/1. The auditory function assessed by thresholds, interpeak intervals and amplitudes of wave I in SAM-P/1 at 12 months of age corresponded roughly to that in SAM-R/1 at 20 months of age. In morphological studies, there was an age-related decrease in the cell density as well as in the size of spiral ganglion neurons in both strains, but these changes were more pronounced in SAM-P/1 than in SAM-R/1. These results reveal that age-related hearing impairment associated with morphological changes in the cochlea is manifested earlier and progresses more rapidly in SAM-P/1 than in SAM-R/1. Thus, the SAM-P/1 strain should prove useful as a model of presbycusis.

UI MeSH Term Description Entries
D008297 Male Males
D008815 Mice, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations, or by parent x offspring matings carried out with certain restrictions. All animals within an inbred strain trace back to a common ancestor in the twentieth generation. Inbred Mouse Strains,Inbred Strain of Mice,Inbred Strain of Mouse,Inbred Strains of Mice,Mouse, Inbred Strain,Inbred Mouse Strain,Mouse Inbred Strain,Mouse Inbred Strains,Mouse Strain, Inbred,Mouse Strains, Inbred,Strain, Inbred Mouse,Strains, Inbred Mouse
D009474 Neurons The basic cellular units of nervous tissue. Each neuron consists of a body, an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the NERVOUS SYSTEM. Nerve Cells,Cell, Nerve,Cells, Nerve,Nerve Cell,Neuron
D011304 Presbycusis Gradual bilateral hearing loss associated with aging that is due to progressive degeneration of cochlear structures and central auditory pathways. Hearing loss usually begins with the high frequencies then progresses to sounds of middle and low frequencies. Presbycuses
D002452 Cell Count The number of CELLS of a specific kind, usually measured per unit volume or area of sample. Cell Density,Cell Number,Cell Counts,Cell Densities,Cell Numbers,Count, Cell,Counts, Cell,Densities, Cell,Density, Cell,Number, Cell,Numbers, Cell
D003051 Cochlea The part of the inner ear (LABYRINTH) that is concerned with hearing. It forms the anterior part of the labyrinth, as a snail-like structure that is situated almost horizontally anterior to the VESTIBULAR LABYRINTH. Cochleas
D004195 Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. Animal Disease Model,Animal Disease Models,Disease Model, Animal
D005260 Female Females
D000375 Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. Senescence,Aging, Biological,Biological Aging
D000704 Analysis of Variance A statistical technique that isolates and assesses the contributions of categorical independent variables to variation in the mean of a continuous dependent variable. ANOVA,Analysis, Variance,Variance Analysis,Analyses, Variance,Variance Analyses

Related Publications

Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
October 1996, Journal of periodontal research,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
September 1996, Brain research,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
September 1982, Mechanisms of ageing and development,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
January 1986, Physiology & behavior,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
May 1992, Physiology & behavior,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
June 1991, Mechanisms of ageing and development,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
January 1993, Neurobiology of aging,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
January 1993, Neurobiology of aging,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
November 1990, The Journal of nutrition,
Y Saitoh, and M Hosokawa, and A Shimada, and Y Watanabe, and N Yasuda, and T Takeda, and Y Murakami
September 1991, Journal of the American Geriatrics Society,
Copied contents to your clipboard!