Effects of exposing DBA/2J mice to a high-frequency augmented acoustic environment on the cochlea and anteroventral cochlear nucleus

Hearing Research

Volumn 216-217, Issue 1-2, 2006, Pages 138-145

  Willott, James F ^a,b   Bosch, Justine Vanden ^a   Shimizu, Toru ^a   Ding, Da Lian ^c  

^a UNIVERSITY OF SOUTH FLORIDA   (United States)

^b JACKSON LABORATORY   (United States)

^c UNIVERSITY AT BUFFALO   (United States)

Author keywords

Augmented acoustic environment; Cochlear nucleus; Hair cells; Mice; Sensorineural hearing loss

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDIOMETRY; AUDITORY NERVOUS SYSTEM; AUDITORY STIMULATION; CELL COUNT; CELL SURVIVAL; COCHLEA; COCHLEAR NUCLEUS; CONTROLLED STUDY; ENVIRONMENT; EVOKED BRAIN STEM AUDITORY RESPONSE; EXPOSURE; FEMALE; FREQUENCY MODULATION; HAIR CELL; HEARING; MALE; MOUSE; NERVE CELL; NOISE; NONHUMAN; PERCEPTION DEAFNESS; PHYSIOLOGY; PRIORITY JOURNAL; SOUND PRESSURE;

ANALYSIS OF VARIANCE; ANIMALS; AUDITORY THRESHOLD; COCHLEA; COCHLEAR NUCLEUS; ENVIRONMENT; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; FEMALE; HEARING LOSS, NOISE-INDUCED; HEARING LOSS, SENSORINEURAL; MALE; MICE; MICE, INBRED DBA; NOISE; RANDOM ALLOCATION;

EID: 33744967738     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.heares.2006.01.010     Document Type: Article

References (41)

1. Berglund A.M., and Brown M.C. Central trajectories of type II spiral ganglion cells from various cochlear regions in mice. Hear. Res. 75 (1994) 121-130
2. Blatchley B.J., Williams J.E., and Coleman J.R. Age-dependent effects of acoustic deprivation on spherical cells in the rat anteroventral cochlear nucleus. Exper. Neurol. 80 (1983) 81-93
3. Coleman J.R., and O'Connor P. Effects of monaural and binaural sound deprivation on cell development in the anteroventral cochlear nucleus of rats. Exper. Neurol. 64 (1979) 553-566
4. Bohne B., Harding G.W., and Ou H.C. Preparation and evaluation of the mouse temporal bone. In: Willott J.F. (Ed). Handbook of Mouse Auditory Research (2001), CRC Press, Boca Raton 171-187
5. Ding D., McFadden S.L., and Salvi R.J. Cochlear hair cell densities and inner-ear staining techniques. In: Willott J.F. (Ed). Handbook of Mouse Auditory Research (2001), CRC Press, Boca Raton 189-204
6. Ehret G. Peripheral anatomy and physiology. In: Willott J.F. (Ed). Auditory Psychobiology of the Mouse (1983), Charles C Thomas, Springfield, IL 169-200
7. Erway L.C., Willott J.F., Archer J.R., and Harrison D. Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains. Hear. Res. 65 (1993) 125-132
8. Hashisaki G.T., and Rubel E.W. Effects of unilateral cochlear removal on anteroventral cochlear nucleus neurons in developing gerbils. J. Comp. Neurol. 283 (1989) 465-473
9. Frisina R.D., and Walton J.P. Neuroanatomy of the central auditory system. In: Willott J.F. (Ed). Handbook of Mouse Auditory Research (2001), CRC Press, Boca Raton 243-278
10. Henry K.R., and Chole R.A. Genotypic differences in behavioral, physiological and anatomical expressions of age-related hearing loss in the laboratory mouse. Audiology 1 (1980) 369-383
11. Javel E. Basic response properties of auditory nerve fibers. In: Altschuler R.A., Hoffman D.W., and Bobbin R.P. (Eds). Neurobiology of Hearing: The Cochlea (1986), Raven Press, New York 213-245
12. Johnson K.R., Erway L.C., Cook S.A., Willott J.F., and Zheng Q.Y. A major gene affecting age-related hearing loss in C57BL/6J mice. Hear. Res. 114 (1997) 83-92
13. Johnson K.R., Zheng Q.Y., and Erway L.C. A major gene affecting age-related hearing loss is common to at least 10 inbred strains of mice. Genomics 70 (2000) 171-180
14. Kiang, N.Y.S., Watanabe, T., Thomas, E.C., Clark, L.F., 1965. Discharge Patterns Of Single Fibers In The Cat's Auditory Nerve. M.I.T. Research Monograph No. 35, M.I.T. Press, Cambridge, MA.
15. McFadden S.L., Ding D., Reaume A.G., Flood D.G., and Salvi R.J. Age-related cochlear hair cell loss is enhanced in mice lacking copper/zinc superoxide dismutase. Neurobiol. Aging 20 (1999) 1-8
16. McFadden S.L., Ding D., Burkard R.F., Jiang H., Reaume A.G., Flood D.G., and Salvi R.J. Cu/Zn SOD deficiency potentiates hearing loss and cochlear pathology in aged 129,CD-1 mice. J. Comp. Neurol. 413 (1999) 101-112
17. Norena A.J., and Eggermont J.J. Enriched acoustic environment after noise trauma reduces hearing loss and prevents cortical map reorganization. J. Neurosci. 25 (2005) 699-705
18. Ralls K. Auditory sensitivity in mice: Peromyscus and Mus musculus. Anim. Behav. 15 (1967) 123-128
19. Ramon y Cajal S. L'Histologie du Systeme Nerveux de l'Homme et des Vertebres (1909), A. Maloine, Paris
20. Rhode W.S. Physiological-morphological properties of the cochlear nucleus. In: Altschuler R.A., Bobbin R.P., Clopton B.M., and Hoffman D.W. (Eds). Neurobiology of Hearing: The Central Auditory System (1991), Raven Press, New York 47-77
21. Ryugo D.K., Willard F.H., and Fekete D.M. Differential afferent projections to the inferior colliculus from the cochlear nucleus in the albino mouse. Brain. Res. 210 (1981) 342-349
22. Shnerson A., and Pujol R. Development: anatomy, electrophysiology, and behavior. In: Willott J.F. (Ed). Auditory Psychobiology of the Mouse (1983), Charles C Thomas, Springfield, IL 395-425
23. Spongr V.P., Flood D.G., Frisina R.D., and Salvi R.J. Quantitative measures of hair cell loss in CBA and C57BL/6 mice throughout their life spans. J. Acoust. Soc. Amer. 101 (1997) 3546-3553
24. Sundin V., and Willott J.F. Effects of exposure to an augmented acoustic environment on hearing loss in DBA/2J mice: frequency specificity (1999), Society for Neuroscience, Miami
25. Trettel J., and Morest K.D. Cytoarchitectonic atlas of the cochlear nucleus of the mouse. In: Willott J.F. (Ed). Handbook of Mouse Auditory Research (2001), CRC Press, Boca Raton 279-298
26. Trune D.R. Influence of neonatal cochlear removal on the development of mouse cochlear nucleus: I. Number, size, and density of its neurons. J. Comp. Neurol. 209 (1982) 409-424
27. Turner J.G., and Willott J.F. Exposure to an augmented acoustic environment alters progressive hearing loss in DBA/2J mice. Hear. Res. 118 (1998) 101-113
28. Webster D.B. Auditory neuronal sizes after a unilateral conductive hearing loss, Exper. Neurology 79 (1983) 130-140
29. Webster D.B. Conductive hearing loss affects the growth of the cochlear nuclei over an extended period of time. Hear. Res. 32 (1988) 185-192
30. Webster D.B., and Webster M. Effects of neonatal conductive hearing loss on brain stem auditory nuclei. Ann. Otol. Rhinol. Laryngol. 88 (1979) 684-688
31. Willott J.F. Comparison of response properties of inferior colliculus neurons of two inbred mouse strains differing in susceptibility to audiogenic seizures. J. Neurophysiol. 45 (1981) 35-47
32. Willott J.F. Aging and the auditory system. In: Mohr U., Dungworth D.L., Capen C.C., Carlton W.W., Sundberg J.P., and Ward J.M. (Eds). Pathobiology of the Aging Mouse, ILSI Monographs on the Pathobiology of Aging Animals (1996), ILSI Press, Washington, DC 179-204
33. Willott J.F., and Bross L.S. Morphological changes in the anteroventral cochlear nucleus that accompany sensorineural hearing loss in DBA/2J and C57BL/6J mice. Brain Res. Dev. Brain Res. 91 (1996) 218-226
34. Willott J.F., and Bross L.S. Effects of prolonged exposure to an augmented acoustic environment on the auditory system of middle-aged C57BL/6J mice: cochlear and central histology and sex differences. J. Comp. Neurol. 472 (2004) 358-370
35. Willott J.F., Bross L.S., and McFadden S.L. Ameliorative effects of exposing DBA/2J mice to an augmented acoustic environment on histological changes in the cochlea and anteroventral cochlear nucleus. J. Assoc. Res. Otolaryngol. 28 (2005) 1-10
36. Willott J.F., Demuth R.M., Lu S.M., and Van Bergem P. Abnormal tonotopic organization in the ventral cochlear nucleus of the hearing-impaired DBA/2 mouse. Neurosci. Lett. 34 (1982) 13-17
37. Willott J.F., Jackson L.M., and Hunter K.P. Morphometric study of the anteroventral cochlear nucleus of two mouse models of presbycusis. J. Comp. Neurol. 260 (1987) 472-480
38. Willott J.F., Kulig J., and Satterfield T. The acoustic startle response in DBA/2 and C57BL/6 mice: relationship to auditory neuronal response properties and hearing impairment. Hear. Res. 16 (1984) 161-167
39. Willott J.F., and Turner J.G. Prolonged exposure to an augmented acoustic environment ameliorates age-related auditory changes in C57BL/6J and DBA/2J mice. Hear. Res. 135 (1999) 78-88
40. Willott J.F., and Turner J.G. Neural plasticity in the mouse inferior colliculus: Relationship to hearing loss, augmented acoustic stimulation, and prepulse inhibition. Hear. Res. 147 (2000) 275-281
41. Willott J.F., Turner J.G., and Sundin V.S. Effects of exposure to an augmented acoustic environment on auditory function in mice: Roles of hearing loss and age during treatment. Hear. Res. 142 (2000) 79-88