The effects of early bilateral deafening on calretinin expression in the dorsal cochlear nucleus of aged CBA/CaJ mice

Hearing Research

Volumn 183, Issue 1-2, 2003, Pages 57-66

  Zettel, Martha L ^a   O'Neill, William E ^a   Trang, Tung T ^b   Frisina, Robert D ^a  

^a UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

^b UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

Author keywords

Auditory midbrain; Calcium binding protein; Neural plasticity; Presbycusis

Indexed keywords

CALRETININ; KANAMYCIN;

AGE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; AUDITORY NERVOUS SYSTEM; BRAIN STEM; CELL COUNT; CELL DENSITY; COCHLEAR NUCLEUS; CONTROLLED STUDY; DATA ANALYSIS; DISEASE SEVERITY; EVOKED AUDITORY RESPONSE; FEMALE; HEARING ACUITY; HEARING LOSS; IMMUNOREACTIVITY; MALE; MOUSE; NONHUMAN; PREDICTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; SOUND; STATISTICAL SIGNIFICANCE;

EID: 0141790271     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(03)00216-8     Document Type: Article

References (40)

1. Batini C., Palestini M., Thomasset M., Vigot R. Cytoplasmic calcium buffer, calbindin-D28k, is regulated by excitatory amino acids. NeuroReport. 4:1993;927-930.
2. Billing-Marczak K., Kuznicki J. Calretinin-sensor or buffer-function still unclear. Polish J. Pharm. 51:1999;173-178.
3. Braun A.K., Rogers J.H., Rubel E.W. Activity-dependent changes of calretinin-immunoreactivity in the auditory brainstem of the chick. Assoc. Res. Otolaryngol. 13:1990;388-389.
4. Caicedo A., d'Aldin C., Eybalin M., Puel J.L. Temporary sensory deprivation changes calcium-binding proteins levels in the auditory brainstem. J. Comp. Neurol. 378:1997;1-15.
5. Durham D., Rubel E.W., Steel K.P. Cochlear ablation in deafness mutant mice: 2-deoxyglucose analysis suggests no spontaneous activity of cochlear origin. Hear. Res. 43:1989;39-46.
6. Dutar P., Potier B., Lamour Y., Emson P.C., Senut M.C. Loss of calbindin-28k immunoreactivity in hippocampal slices from aged rats: A role for calcium? Eur. J. Neurosci. 3:1991;839-849.
7. Forster C.R., Illing R.B. Plasticity of the auditory brainstem: cochleotomy-induced changes of calbindin-D28k expression in the rat. J. Comp. Neurol. 416:2000;173-187.
8. Frisina, D.R., Frisina, R.D., Snell, K.B., Burkard, R., Walton, J.P., Ison, J.R., 2001. Auditory temporal processing during aging. In: Hof, P.R., Mobbs, C.V. (Eds.), Functional Neurobiology of Aging. Academic Press, San Diego, CA, chapter 39, pp. 565-579.
9. Frisina, R.D., Walton, J.P., 2001. Aging of the mouse central auditory system. In: Willott, J.P. (Ed.), Handbook of Mouse Auditory Research: From Behavior to Molecular Biology. CRC Press, New York, chapter 24, pp. 339-379.
10. Garcia M.M., Harlan R.E. Chronic morphine increases calbindin D28k in rat striatum: possible NMDA receptor involvement. NeuroReport. 5:1993;65-68.
11. German D.C., Manaye K.F., Sonsalla P.K., Brooks B.A. Midbrain dopaminergic cell loss in Parkinson's disease and MPTP-induced Parkonsonism: Sparing of calbindin-D28k-containing cells. Ann. NY Acad. Sci. 648:1992;42-62.
12. Hack N.J., Wride M.C., Charters K.M., Kater S.B., Parks T.N. Developmental changes in the subcellular localization of calretinin. J. Neurosci. 20:2000;1-5.
13. Huang Q., Zhou D., Sapp E., Aizawa H., Ge P., Bird E.D., Vonsattel J.P., DiFiglia M. Quinolinic acid-induced increases in calbindin D28k immunoreactivity in rat striatal neurons in vivo and in vitro mimic the pattern seen in Huntington's disease. Neuroscience. 65:1995;397-407.
14. Hugon J., Hugon F., Esclaire F., Lesort M., Diop A.G. The presence of calbindin in rat cortical neurons protects in vitro from oxydative stress. Brain Research. 707:1996;288-292.
15. Iacopino A., Christakos S., German D., Sonsalla P.K., Altar C.A. Calbindin-D28k-containing neurons in animal models of neurodegeneration: possible protection from excitotoxicity. Mol. Brain Res. 13:1992;251-261.
16. Iacopino A.M., Christakos S. Specific reduction of calcium-binding protein (28-kilodalton calbindin-D) gene expression in aging and neurodegenerative diseases. Proc. Natl. Acad. Sci. USA. 87:1990;4078-4082.
17. Idrizbegovic E., Bogdanovic N., Canlon B. Modulating calbindin and parvalbumin immunoreactivity in the cochlear nucleus by moderate noise exposure in mice. A quantitative study on the dorsal and posteroventral cochlear nucleus. Brain Res. 800:1998;86-96.
18. Idrizbegovic, E., Bogdanovic, N., Canlon, B., 2001. Calcium binding proteins in the central auditory system: Modulation by noise exposure and aging. In: Willott, J.P. (Ed.), Handbook of Mouse Auditory Research: From Behavior to Molecular Biology. CRC Press, Boca Raton, FL, chapter 22, pp. 321-330.
19. Koerber K.C., Pfeiffer R.R., Warr W.B., Kiang N.Y. Spontaneous spike discharges from single units in the cochlear nucleus after destruction of the cochlea. Exp. Neurol. 16:1966;119-130.
20. Kurobe N., Inaguma Y., Shinohara H., Semba R., Inagaki T., Kato K. Developemental and age-dependent changes of 28-kDa Calbindin-D in the central nervous tissue determined with a sensitive immunoassay method. J. Neurochem. 58:1992;128-134.
21. Lowenstein D.H., Miles M.F., Hatam F., McCabe T. Up regulation of calbindin-D28k mRNA in the rat hippocampus following focal stimulation of the perforant path. Neuron. 6:1991;627-633.
22. Lukas W., Jones K.A. Cortical neurons containing calretinin are selectively resistant to calcium overload and excitotoxicity in vitro. Neuroscience. 61:1994;307-316.
23. Mattson M.P., Rychlik B., Chu C., Christakos S. Evidence for calcium-reducing and excito-protective roles for the calcium binding protein calbindin D-28k in cultured hippocampal neurons. Neuron. 6:1991;41-51.
24. Mugnaini E., Warr W.B., Osen K.K. Distribution and light microscopic features of granule cells in the cochlear nuclei of cat, rat, and mouse. J. Comp. Neurol. 191:1980;581-606.
25. O'Neill W.E., Zettel M.L., Whittemore K.R., Frisina R.D. Calbindin D-28k immunoreactivity in the medial nucleus of the trapezoid body declines with age in C57BL/6, but not CBA/CaJ mice. Hear. Res. 112:1997;158-166.
26. Rubel E.W., Hyson R.L., Durham D. Afferent regulation of neurons in the brain stem auditory system. J. Neurobiol. 21:1990;169-196.
27. Ryugo D.K., Willard F.H. The dorsal cochlear nucleus of the mouse: a light microscopic analysis of neurons that project to the inferior colliculus. J. Comp. Neurol. 242:1985;381-396.
28. Sans N., Moniot B., Raymond J. Distribution of calretinin mRNA in the vestibular nuclei of rat and guinea pig and the effects of unilateral labyrinthectomy: a non-radioactive in situ hybridization study [published erratum appears in Brain Res. Mol. Brain Res. 30, 1995, 177-179]. Mol. Brain Res. 28:1995;1-11.
29. Seftel M.A., Deitch J.S., Rubel E.W. Immunocytochemical analysis of cytoskeletal proteins in normal and deafferented nucleus magnocellualaris neurons. Assoc. Res. Otolaryngol. 9:1986;8-9.
30. Varghese G., Zettel M.L., Roeut R., Frisina R.D. Age related declines in calbindin expression in the ventral cochlear nucleus of deafened and hearing CBA/CaJ and C57Bl/6 mice. Assoc. Res. Otolaryngol. Abstr. 26:2003;50.
31. Webster D.B., Trune D.R. Cochlear nuclear complex of mice. Am. J. Anat. 163:1982;103-130.
32. Willard, F.H., Ryugo, D.K., 1983. Anatomy of the central auditory system. In: Willott, J.F. (Ed.), The Auditory Psychobiology of the Mouse. Thomas, Springfield, IL, pp. 201-304.
33. Willott J.F., Parham K., Hunter K.P. Response properties of inferior colliculus neurons in middle-aged C57BL/6J mice with presbycusis. Hear. Res. 37:1988;15-27.
34. Willott J.F., Bross L.S., McFadden S.L. Morphology of the dorsal cochlear nucleus in C57BL/6J and CBA/J mice across the life span. J. Comp. Neurol. 321:1992;666-678.
35. Willott J.F., Bross L.S., McFadden S.L. Morphology of the cochlear nucleus in CBA/J mice with chronic, severe sensorineural cochlear pathology induced during adulthood. Hear. Res. 74:1994;1-21.
36. Winsky L., Jacobowitz D.M. Effects of unilateral cochlea ablation on the distribution of calretinin mRNA and immunoreactivity in the guinea pig ventral cochlear nucleus. J. Comp. Neurol. 354:1995;564-582.
37. Zettel M.L., Frisina R.D., Haider S.E., O'Neill W.E. Age-related changes in calbindin D-28k and calretinin immunoreactivity in the inferior colliculus of CBA/CaJ and C57Bl/6 mice. J. Comp. Neurol. 386:1997;92-110.
38. Zettel M.L., O'Neill W.E., Frisina R.D. Deafened, then aged, CBA mice have fewer calretinin positive cells in DCN than young hearing or aged hearing CBA mice. Assoc. Res. Otolaryngol. 24:2001.
39. Zettel M.L., O'Neill W.E., Trang T.T., Frisina R.D. Early bilateral deafening prevents calretinin up-regulation in the dorsal cortex of the inferior colliculus of aged CBA/CaJ mice. Hear. Res. 158:2001;131-138.
40. Zirpel L., Lachica E.A., Lippe W.R. Deafferentation increases the intracellular calcium of cochlear nucleus neurons in the embryonic chick. J. Neurophysiol. 74:1995;1355-1357.