Central anatomical correlates of aging and age-related hearing loss (presbycusis) will be studied in two mouse models: the C57BL/6J, which demonstrates progressive sensorineural hearing loss (SNHL) with onset during young adulthood to middle age; and the CBA/J, which maintains good auditory sensitivity until late in life. Several age groups will be studied, ranging from young (2-months old) to very old (over 30-months). Two groups of CBA mice with induced chronic SNHL (similar to that occurring in C57 mice) will also be employed. Quantitative morphometric evaluations will be made in subdivisions of the cochlear nucleus (CN) and inferior colliculus (IC) using Nissl-stained, fiber-stained, and Golgi- impregnated tissue. A variety of cellular features will be assessed including cell number (neurons and glia), neuronal soma size and shape, dendritic dimensions and orientation, presence of spines, signs of degeneration, etc. Data will be statistically analyzed as a function of age, brainstem subnucleus, and when appropriate, cell type or location with regard to tonotopic organization. Peripheral input to the brainstem will be evaluated using quantitative counts of spiral ganglion cells. The final product will be a comprehensive, detailed anatomical description of two major auditory brainstem regions in two mouse models of presbycusis. In addition, by comparisons among data from the various subject groups the contributions of aging per se, the occurrence and chronicity of SNHL, and genotype will be elucidated.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AG007554-08
Application #
2049791
Study Section
Special Emphasis Panel (NSS)
Project Start
1988-05-01
Project End
1998-04-30
Budget Start
1995-05-01
Budget End
1996-04-30
Support Year
8
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Northern Illinois University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
City
De Kalb
State
IL
Country
United States
Zip Code
60115
Idrizbegovic, Esma; Bogdanovic, Nenad; Willott, James F et al. (2004) Age-related increases in calcium-binding protein immunoreactivity in the cochlear nucleus of hearing impaired C57BL/6J mice. Neurobiol Aging 25:1085-93
Gauthier, K; Plateroti, M; Harvey, C B et al. (2001) Genetic analysis reveals different functions for the products of the thyroid hormone receptor alpha locus. Mol Cell Biol 21:4748-60
Idrizbegovic, E; Canlon, B; Bross, L S et al. (2001) The total number of neurons and calcium binding protein positive neurons during aging in the cochlear nucleus of CBA/CaJ mice: a quantitative study. Hear Res 158:102-15
Falls, W A; Kogan, J H; Silva, A J et al. (2000) Fear-potentiated startle, but not prepulse inhibition of startle, is impaired in CREBalphadelta-/- mutant mice. Behav Neurosci 114:998-1004
Willott, J F; Turner, J G (2000) Neural plasticity in the mouse inferior colliculus: relationship to hearing loss, augmented acoustic stimulation, and prepulse inhibition. Hear Res 147:275-81
Jeskey, J E; Willott, J F (2000) Modulation of prepulse inhibition by an augmented acoustic environment in DBA/2J mice. Behav Neurosci 114:991-7
Parham, K; Bonaiuto, G; Carlson, S et al. (2000) Purkinje cell degeneration and control mice: responses of single units in the dorsal cochlear nucleus and the acoustic startle response. Hear Res 148:137-52
Heldt, S; Sundin, V; Willott, J F et al. (2000) Posttraining lesions of the amygdala interfere with fear-potentiated startle to both visual and auditory conditioned stimuli in C57BL/6J mice. Behav Neurosci 114:749-59
Willott, J F; Turner, J G (1999) Prolonged exposure to an augmented acoustic environment ameliorates age-related auditory changes in C57BL/6J and DBA/2J mice. Hear Res 135:78-88
Turner, J G; Willott, J F (1998) Exposure to an augmented acoustic environment alters auditory function in hearing-impaired DBA/2J mice. Hear Res 118:101-13

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