It is generally believed that the cochlea is able to encode sound stimuli by using an active negative damping mechanism to overcome problems inherent in the physical constraints of the system. This active process is responsible for the sharp tuning and low thresholds observed in the response to auditory stimuli. Outer hair cells (OHCs) are the cellular elements responsible for generating the active process and are under the influence of descending efferent fibers originating in the brainstem. Numerous studies have shown that the major neurotransmitter at the OHC/efferent terminal synapse is ACh. We have cloned a novel ACh receptor, designated [alpha]9, which has the same pharmacological profile as that reported earlier for the OHC cholinergic receptor. In order to better understand how cochlear functions are accomplished, a study of the [alpha]9 nAChR subunit is necessary. Efferent effects on the cochlea have usually been studied through electrical stimulation of the olivocochlear bundle (OCB). However, in order to elicit a response, high stimulus rates must be used which are higher than the natural OCB activity. Another way to study the effects of efferent activation on the cochlea (and thus the study of the OHC-efferent fiber synapse) has been to pharmacologically manipulate the system, but the selectivity and specificity of drugs is always a concern in vivo. Therefore, in order to directly examine the role [alpha]9 has in the cochlea, we have designed a series of experiments which make use of animals carrying null allele mutations for the [alpha]9 gene. Our long-term goal is to understand the cochlear efferent system and how it contributes to normal hearing processes. Thus, we will begin a series of investigations into the anatomical and physiological consequences of [alpha]9 ablation.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC002871-03
Application #
2749249
Study Section
Hearing Research Study Section (HAR)
Project Start
1996-08-01
Project End
2000-07-31
Budget Start
1998-08-01
Budget End
1999-07-31
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Salk Institute for Biological Studies
Department
Type
DUNS #
005436803
City
La Jolla
State
CA
Country
United States
Zip Code
92037
He, David Z Z; Cheatham, Mary Ann; Pearce, Malini et al. (2004) Mouse outer hair cells lacking the alpha9 ACh receptor are motile. Brain Res Dev Brain Res 148:19-25
Elgoyhen, A B; Vetter, D E; Katz, E et al. (2001) alpha10: a determinant of nicotinic cholinergic receptor function in mammalian vestibular and cochlear mechanosensory hair cells. Proc Natl Acad Sci U S A 98:3501-6
Vetter, D E; Liberman, M C; Mann, J et al. (1999) Role of alpha9 nicotinic ACh receptor subunits in the development and function of cochlear efferent innervation. Neuron 23:93-103
Vetter, D E; Mann, J R; Wangemann, P et al. (1996) Inner ear defects induced by null mutation of the isk gene. Neuron 17:1251-64