Inner ear lesions result in permanent deficiencies in balance and hearing. It is therefore important to reduce or eliminate the lesions that are accompanied by a variety of insults to the inner ear. Neurotrophic factors have been shown to protect inner ear structure and function against acoustic and ototoxic trauma. One neurotrophic factor, the Glial cell-line derived neurotrophic factor (GDNF) demonstrated a robust protective effect against trauma in the inner ear of the guinea pig. The experiments in this grant are designed to continue to characterize the protective effect of GDNF in the auditory and vestibular systems, and to extend the data to a different animal model, the mouse. The experiments will use gene transfer technology for GDNF transgene over-expression in the inner ear. Specifically, we propose to (a) determine the protective effect of GDNF on the mouse auditory and vestibular epithelia using electrophysiological, behavioral and morphological analyses, (b) determine the cells types that bind GDNF in normal and traumatized inner ear tissues and (c) shed light on the genes that are involved in the downstream signaling cascade of GDNF. The data we propose to generate will enhance our understanding of the mechanisms of action of GDNF in normal and injured inner ear epithelia, knowledge that may eventually lead to better clinical treatments

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
1R01DC005401-01
Application #
6464176
Study Section
Special Emphasis Panel (ZRG1-IFCN-6 (01))
Program Officer
Freeman, Nancy
Project Start
2002-09-01
Project End
2006-07-31
Budget Start
2002-09-01
Budget End
2004-07-31
Support Year
1
Fiscal Year
2002
Total Cost
$308,729
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Chikar, Jennifer A; Hendricks, Jeffrey L; Richardson-Burns, Sarah M et al. (2012) The use of a dual PEDOT and RGD-functionalized alginate hydrogel coating to provide sustained drug delivery and improved cochlear implant function. Biomaterials 33:1982-90
Kawamoto, Kohei; Izumikawa, Masahiko; Beyer, Lisa A et al. (2009) Spontaneous hair cell regeneration in the mouse utricle following gentamicin ototoxicity. Hear Res 247:17-26
Chikar, Jennifer A; Batts, Shelley A; Pfingst, Bryan E et al. (2009) Visualization of spiral ganglion neurites within the scala tympani with a cochlear implant in situ. J Neurosci Methods 179:201-7
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Mustapha, Mirna; Fang, Qing; Gong, Tzy-Wen et al. (2009) Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants. J Neurosci 29:1212-23
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Hendricks, Jeffrey L; Chikar, Jennifer A; Crumling, Mark A et al. (2008) Localized cell and drug delivery for auditory prostheses. Hear Res 242:117-31
Izumikawa, Masahiko; Batts, Shelley A; Miyazawa, Toru et al. (2008) Response of the flat cochlear epithelium to forced expression of Atoh1. Hear Res 240:52-6
Chikar, Jennifer A; Colesa, Deborah J; Swiderski, Donald L et al. (2008) Over-expression of BDNF by adenovirus with concurrent electrical stimulation improves cochlear implant thresholds and survival of auditory neurons. Hear Res 245:24-34
Rejali, Darius; Lee, Valerie A; Abrashkin, Karen A et al. (2007) Cochlear implants and ex vivo BDNF gene therapy protect spiral ganglion neurons. Hear Res 228:180-7

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