The central vestibular system exhibits a remarkable natural recovery of many functions after peripheral vestibular lesions. The first brain centers involved in this plasticity are the vestibular nuclei, and their integrity is crucial for recovery. The major goal of this work is to understand how excitability and synaptic transmission change in an identified class of vestibular nucleus neurons during compensation from unilateral vestibular ganglionectomy's. The chick tangential nucleus (lateral vestibular nucleus) will be studied in brain slices of hatchling chicks and in whole animals. Its principal cells participate in two vestibular reflexes affected by the lesion, but show recovery. We propose that changes in synaptic and intrinsic membrane properties and/or dendritic terminals may occur in vestibular nuclei during compensation. The techniques include patch-clamp recording in brain slices, pharmacological testing, and immunolabeling combined with confocal imaging. Lesion will be made in hatchling chicks (4-5 days postnatal) that are sacrificed at selected stages during compensation (6, 12, 24 hours; 3 and 7 days after surgery). By H4-5, the mature firing pattern, including spontaneous spike firing and evoked repetitive firing, is established in these neurons.
The specific aims i nclude whole-cell patch-clamp recordings of spontaneous spike firing, spontaneous synaptic activity, and voltage-gated outward potassium currents in the ipsi- and contra lateral tangential principal cells, studies on vestibular-evoked spike firing and synaptic currents in the contra lateral tangential principal cells, and immunocytochemical studies of AMPA receptor subunits (GluR1, GluR2, GluR2/3, GluR4), potassium (Kv1.1, Kv1.2) and gap junction channels (connexins) in the ipsi- and contra lateral tangential nucleus. The scope of the study will be broadened by sampling other vestibular neurons likely to contribute to compensation, including elongate cells of the tangential nucleus and cell type B of the medial vestibular nucleus. For the first time, signal processing will be studied using state-of-art methods in a homogeneous, morphologically identified group of vestibular nucleus neurons at selected times during behavioral recovery from unilateral vestibular ganglionectomy's. As the basic mechanisms controlling excitability and synaptic transmission in vestibular nucleus neurons are better understood and molecular targets are identified, more effective therapies will be devised to treat central vestibular disorders resulting from disease, injury and aging.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC000970-17
Application #
7442298
Study Section
Auditory System Study Section (AUD)
Program Officer
Cyr, Janet
Project Start
1991-04-01
Project End
2009-09-02
Budget Start
2008-07-01
Budget End
2009-09-02
Support Year
17
Fiscal Year
2008
Total Cost
$325,748
Indirect Cost
Name
George Washington University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
043990498
City
Washington
State
DC
Country
United States
Zip Code
20052
Shao, Mei; Hirsch, June C; Peusner, Kenna D (2012) Plasticity of spontaneous excitatory and inhibitory synaptic activity in morphologically defined vestibular nuclei neurons during early vestibular compensation. J Neurophysiol 107:29-41
Shao, M; Reddaway, R; Hirsch, J C et al. (2012) Presynaptic GABA(B) receptors decrease neurotransmitter release in vestibular nuclei neurons during vestibular compensation. Neuroscience 223:333-54
Popratiloff, A; Peusner, K D (2011) GABA and glycine immunolabeling in the chicken tangential nucleus. Neuroscience 175:328-43
Popratiloff, Anastas; Shao, Mei; Hirsch, June C et al. (2011) Expression of glutamate receptors and potassium channels in vestibular nuclei neurons during development of signal processing. J Vestib Res 21:21-31
Gottesman-Davis, A; Shao, M; Hirsch, J C et al. (2011) Electrophysiological properties of morphologically-identified medial vestibular nucleus neurons projecting to the abducens nucleus in the chick embryo. Neuroscience 172:494-509
Gottesman-Davis, Adria; Peusner, Kenna D (2010) Identification of vestibuloocular projection neurons in the developing chicken medial vestibular nucleus. J Neurosci Res 88:290-303
Shao, M; Popratiloff, A; Yi, J et al. (2009) Adaptation of chicken vestibular nucleus neurons to unilateral vestibular ganglionectomy. Neuroscience 161:988-1007
Shao, Mei; Popratiloff, Anastas; Hirsch, June C et al. (2009) Presynaptic and postsynaptic ion channel expression in vestibular nuclei neurons after unilateral vestibular deafferentation. J Vestib Res 19:191-200
Shao, M; Gottesman-Davis, A; Popratiloff, A et al. (2008) Dye coupling in developing vestibular nuclei. J Neurosci Res 86:832-44
Shao, M; Hirsch, J C; Peusner, K D (2006) Maturation of firing pattern in chick vestibular nucleus neurons. Neuroscience 141:711-26

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