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June 2000, Volume 7, Number 12, Pages 1046-1054
Table of contents    Previous  Abstract  Next   Full text  PDF
Viral transfer technology
Effect of transgenic GDNF expression on gentamicin-induced cochlear and vestibular toxicity
M Suzuki1,2, M Yagi1,3, J N Brown1, A L Miller1, J M Miller1 and Y Raphael1

1Kresge Hearing Research Institute, The University of Michigan, Ann Arbor, MI, USA

2Department of Otolaryngology, University of Tokyo, Tokyo, Japan

3Department of Otolaryngology, Kansai Medical University, Osaka, Japan

Correspondence to: Y Raphael, Room 9303, MSRB III, The University of Michigan, Ann Arbor, MI 48109-0648, USA

Abstract

Gentamicin administration often results in cochlear and/or vestibular hair cell loss and hearing and balance impairment. It has been demonstrated that adenovirus-mediated overexpression of glial cell line-derived neurotrophic factor (GDNF) can protect cochlear hair cells against ototoxic injury. In this study, we evaluated the protective effects of adenovirus-mediated overexpression of GDNF against gentamicin ototoxicity. An adenovirus vector expressing the human GDNF gene (Ad.GDNF) was administered into the scala vestibuli as a rescue agent at the same time as gentamicin, or as a protective agent, 7 days before gentamicin administration. Animals in the Rescue group displayed hearing thresholds that were significantly better than those measured in the Gentamicin or Ad.LacZ/Gentamicin groups. In the Protection group, Ad.GDNF afforded significant preservation of utricular hair cells. The data demonstrated protection of the inner ear structure, and rescue of the inner ear structure and function against ototoxic insults. These experiments suggest that inner ear gene therapy may be developed as a clinical tool for protecting the ear against environmentally induced insults. Gene Therapy (2000) 7, 1046-1054.

Keywords

adenovirus; gene transfer; GDNF; gentamicin; cochlea; utricle

Received 12 August 1999; accepted 5 February 2000
June 2000, Volume 7, Number 12, Pages 1046-1054
Table of contents    Previous  Abstract  Next   Full text  PDF
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