Differential impact of temporary and permanent noise-induced hearing loss on neuronal cell density in the mouse central auditory pathway

Journal of Neurotrauma

Volumn 27, Issue 8, 2010, Pages 1499-1507

  Gröschel, Moritz ^a   Götze, Romy ^a   Ernst, Arne ^a   Basta, Dietmar ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

central auditory system; neuronal cell density; noise induced hearing loss; permanent threshold shift; temporary threshold shift

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUDITORY CORTEX; AUDITORY NERVOUS SYSTEM; AUDITORY THRESHOLD SHIFT; CELL DENSITY; COCHLEAR NUCLEUS; CONTROLLED STUDY; EVOKED BRAIN STEM AUDITORY RESPONSE; FEMALE; HEARING LOSS; INFERIOR COLLICULUS; MALE; MEDIAL GENICULATE BODY; MOUSE; NERVE CELL; NOISE; NOISE INDUCED HEARING LOSS; NONHUMAN;

ANIMALS; AUDITORY CORTEX; AUDITORY PATHWAYS; AUDITORY THRESHOLD; CELL COUNT; COCHLEAR NUCLEUS; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; FEMALE; GENICULATE BODIES; HEARING LOSS, NOISE-INDUCED; INFERIOR COLLICULI; MALE; MICE; NEURONS; TISSUE FIXATION;

EID: 77955876432     PISSN: 08977151     EISSN: None     Source Type: Journal    
DOI: 10.1089/neu.2009.1246     Document Type: Article

References (54)

1. Aarnisalo, A.A., Pirvola, U., Liang, X.Q., Miller, J., and Ylikoski, J. (2000). Apoptosis in auditory brainstem neurons after a severe noise trauma of the organ of Corti: intracochlear GDNF treatment reduces the number of apoptotic cells. ORL J. Otorhinolaryngol. Relat. Spec. 62, 330-334.
2. Arundine, M., and Tymianski, M. (2003). Molecular mechanisms of calcium-dependent neurodegeneration in excitotoxicity. Cell Calcium 34, 325-337.
3. Basta, D., and Ernst, A. (2005). Erratum to ";Noise-induced changes of neuronal spontaneous activity in mice inferior colliculus brain slices."; Neurosci. Lett. 374, 74-79.
4. Basta, D., Tzschentke, B., and Ernst, A. (2005). Noise-induced cell death in the mouse medial geniculate body and primary auditory cortex. Neurosci. Lett. 381, 199-204.
5. Benson, C.G., Gross, J.S., Suneja, S.K., and Potashner, S.J. (1997). Synaptophysin immunoreactivity in the cochlear nucleus after unilateral cochlear or ossicular removal. Synapse 25, 243-257.
6. Chen, Z., Peppi, M., Kujawa, S.G., and Sewell, W.F. (2009). Regulated expression of surface AMPA receptors reduces excitotoxicity in auditory neurons. J. Neurophysiol. 102, 1152-1159.
7. Dahmen, J.C., and King, A.J. (2007). Learning to hear: plasticity of auditory cortical processing. Curr. Opin. Neurobiol. 17, 456-464.
8. Ehret, G., and Fischer, R. (1991). Neuronal activity and tonotopy in the auditory system visualized by c-fos gene expression. Brain Res. 567, 350-354.
9. Ferragamo, M.J., and Oertel, D. (2001). Functional circuitry of the cochlear nucleus: In vitro studies in slices, in: Handbook of Mouse Auditory Research. From Behavior to Molecular Biology. J.F. Willott, (ed), CRC Press: Boca Raton, FL, pps. 297-316.
10. Frisina, R.D., and Walton, J.P. (2001). Neuroanatomy of the central auditory system, in: Handbook of Mouse Auditory Research. From Behavior to Molecular Biology. J.F. Willott (ed), CRC Press: Boca Raton, FL, pps. 243-278.
11. Gil-Loyzaga, P., Carricondo, F., Bartolome, M.V., Iglesias, M.C., Rodriguez, F., and Poch-Broto, J. (2010). Cellular and molecular bases of neuroplasticity: brainstem effects after cochlear damage. Acta Otolaryngol. 30, 318-320.
12. Gordon, N. (1995). Apoptosis (programmed cell death) and other reasons for elimination of neurons and axons. Brain Dev. 17, 73-77.
13. Greenwood, S.M., and Connolly, C.N. (2007). Dendritic and mitochondrial changes during glutamate excitotoxicity. Neuropharmacology 53, 891-898.
14. Harris, K.C., Dubno, J.R., Keren, N.I., Ahlstrom, J.B., and Eckert, M.A. (2009). Speech recognition in younger and older adults: a dependency on low-level auditory cortex. J. Neurosci. 29, 6078-6087.
15. Henderson, D., Bielefeld, E.C., Harris, K.C., and Hu, B.H. (2006). The role of oxidative stress in noise-induced hearing loss. Ear Hear. 27, 1-19.
16. Hirose, K., and Liberman, M.C. (2003). Lateral wall histopathology and endocochlear potential in the noise-damaged mouse cochlea. J. Assoc. Res. Otolaryngol. 4, 339-352.
17. Hoya, N., Okamoto, Y., Kamiya, K., Fujii, M., and Matsunaga, T. (2004). A novel animal model of acute cochlear mitochondrial dysfunction. Neuroreport 15, 1597-1600.
18. Hughes, P.E., Alexi, T., Walton, M., Williams, C.E., Dragunow, M., Clark, R.G., and Gluckman, P.D. (1999). Activity and injury-dependent expression of inducible transcription factors, growth factors and apoptosis-related genes within the central nervous system. Prog. Neurobiol. 57, 421-450.
19. Hutchins, J.B., and Barger, S.W. (1998). Why neurons die: cell death in the nervous system. Anat. Rec. 253, 79-90.
20. Jean-Baptiste, M., and Morest, D.K. (1975). Transneuronal changes of synaptic endings and nuclear chromatin in the trapezoid body following cochlear ablations in cats. J. Comp Neurol. 162, 111-134.
21. Kane, E.C. (1974). Patterns of degeneration in the caudal cochlear nucleus of the cat after cochlear ablation. Anat. Rec. 179, 67-91.
22. Kawabata, K., Maeda, S., Takanaga, A., Ito, H., Tanaka, K., Hayakawa, T., and Seki, M. (2003). Apoptosis and retinal projections in the dorsal lateral geniculate nucleus after monocular deprivation during the later phase of the critical period in the rat. Anat. Sci. Int. 78, 104-110.
23. Kim, J.J., Gross, J., Morest, D.K., and Potashner, S.J. (2004). Quantitative study of degeneration and new growth of axons and synaptic endings in the chinchilla cochlear nucleus after acoustic overstimulation. J. Neurosci. Res. 77, 829-842. (Pubitemid 39187066)
24. Kim, J., Morest, D.K., and Bohne, B.A. (1997). Degeneration of axons in the brainstem of the chinchilla after auditory overstimulation. Hear. Res. 103, 169-191.
25. Kotak, V.C., Fujisawa, S., Lee, F.A., Karthikeyan, O., Aoki, C., and Sanes, D.H. (2005). Hearing loss raises excitability in the auditory cortex. J. Neurosci. 25, 3908-3918.
26. Kraus, K.S., Ding, D., Zhou, Y., and Salvi, R.J. (2009). Central auditory plasticity after carboplatin-induced unilateral inner ear damage in the chinchilla: up-regulation of GAP-43 in the ventral cochlear nucleus. Hear. Res. 255, 33-43.
27. Kujawa, S.G., and Liberman, M.C. (2009). Adding insult to injury: cochlear nerve degeneration after ";temporary"; noiseinduced hearing loss. J. Neurosci. 29, 14077-14085.
28. Landgrebe, M., Langguth, B., Rosengarth, K., Braun, S., Koch, A., Kleinjung, T., May, A., de Ridder, R.D., and Hajak, G. (2009). Structural brain changes in tinnitus: grey matter decrease in auditory and non-auditory brain areas. Neuroimage 46, 213-218.
29. Mandairon, N., Jourdan, F., and Didier, A. (2003). Deprivation of sensory inputs to the olfactory bulb up-regulates cell death and proliferation in the subventricular zone of adult mice. Neuroscience 119, 507-516.
30. Mattson, M.P. (2007). Calcium and neurodegeneration. Aging Cell 6, 337-350.
31. Michler, S.A., and Illing, R.B. (2002). Acoustic trauma induces reemergence of the growth- and plasticity-associated protein GAP-43 in the rat auditory brainstem. J. Comp. Neurol. 451, 250-266.
32. Nelson, S.B., and Turrigiano, G.G. (2008). Strength through diversity. Neuron 60, 477-482.
33. Nordmann, A.S., Bohne, B.A., and Harding, G.W. (2000). Histopathological differences between temporary and permanent threshold shift. Hear. Res. 139, 13-30.
34. Nuttall, A.L. (1999). Sound-induced cochlear ischemia/hypoxia as a mechanism of hearing loss. noise. Health 2, 17-32.
35. Paxinos, G., and Franklin, K.B.J. (2001). The Mouse Brain in Stereotaxic Coordinates. Elsevier Science & Technology: Oxford, U.K.
36. Petralia, R.S., Rubio, M.E., Wang, Y.X., and Wenthold, R.J. (2000). Differential distribution of glutamate receptors in the cochlear nuclei. Hear. Res. 147, 59-69.
37. Read, H.L., Winer, J.A., and Schreiner, C.E. (2002). Functional architecture of auditory cortex. Curr. Opin. Neurobiol. 12, 433-440.
38. Ryan, A.F., Axelsson, G.A., and Woolf, N.K. (1992). Central auditory metabolic activity induced by intense noise exposure. Hear. Res. 61, 24-30.
39. Salvi, R.J., Wang, J., and Ding, D. (2000). Auditory plasticity and hyperactivity following cochlear damage. Hear. Res. 147, 261-274.
40. Serrano, F., and Klann, E. (2004). Reactive oxygen species and synaptic plasticity in the aging hippocampus. Ageing Res. Rev. 3, 431-443.
41. Shore, S.E., Koehler, S., Oldakowski, M., Hughes, L.F., and Syed, S. (2008). Dorsal cochlear nucleus responses to somatosensory stimulation are enhanced after noise-induced hearing loss. Eur. J. Neurosci. 27, 155-168.
42. Somjen, G.G. (2001). Mechanisms of spreading depression and hypoxic spreading depression-like depolarization. Physiol Rev. 81, 1065-1096.
43. Suneja, S.K., Yan, L., and Potashner, S.J. (2005). Regulation of NT-3 and BDNF levels in guinea pig auditory brain stem nuclei after unilateral cochlear ablation. J. Neurosci. Res. 80, 381-390.
44. Syka, J., and Rybalko, N. (2000). Threshold shifts and enhancement of cortical evoked responses after noise exposure in rats. Hear. Res. 139, 59-68.
45. Syka, J. (2002). Plastic changes in the central auditory system after hearing loss, restoration of function, and during learning. Physiol Rev. 82, 601-636.
46. Tsuprun, V., Schachern, P.A., Cureoglu, S., and Paparella, M. (2003). Structure of the stereocilia side links and morphology of auditory hair bundle in relation to noise exposure in the chinchilla. J. Neurocytol. 32, 1117-1128.
47. Turrigiano, G.G., Leslie, K.R., Desai, N.S., Rutherford, L.C., and Nelson, S.B. (1998). Activity-dependent scaling of quantal amplitude in neocortical neurons. Nature 391, 892-896.
48. Wagner, W., Heppelmann, G., Kuehn, M., Tisch, M., Vonthein, R., and Zenner, H.P. (2005). Olivocochlear activity and temporary threshold shift-susceptibility in humans. Laryngoscope 115, 2021-2028.
49. Wang, Y., and Manis, P.B. (2008). Short-term synaptic depression and recovery at the mature mammalian endbulb of Held synapse in mice. J. Neurophysiol. 100, 1255-1264.
50. Wang, Y., Hirose, K., and Liberman, M.C. (2002). Dynamics of noise-induced cellular injury and repair in the mouse cochlea. J. Assoc. Res. Otolaryngol. 3, 248-268.
51. Wang, Y.X., Wenthold, R.J., Ottersen, O.P., and Petralia, R.S. (1998). Endbulb synapses in the anteroventral cochlear nucleus express a specific subset of AMPA-type glutamate receptor subunits. J. Neurosci. 18, 1148-1160.
52. Xerri, C., and Zennou-Azogui, Y. (2003). Influence of the postlesion environment and chronic piracetam treatment on the organization of the somatotopic map in the rat primary somatosensory cortex after focal cortical injury. Neuroscience 118, 161-177.
53. Yamashita, D., Jiang, H.Y., Schacht, J., and Miller, J.M. (2004). Delayed production of free radicals following noise exposure. Brain Res. 1019, 201-209.
54. Yu, S.P., Canzoniero, L.M., and Choi, D.W. (2001). Ion homeostasis and apoptosis. Curr. Opin. Cell Biol. 13, 405-411.