A Multifaceted Examination of the Central Processes Underlying Vestibular Compensation

The vestibular system provides us with sensory information that is essential for maintaining balance and stability. When sensory input is lost due to unilateral vestibular damage (UVD), our ability to maintain stable gaze and posture becomes compromised. Over time, vestibular function is partially...

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Main Author: Sweezie, Raquel
Other Authors: Broussard, Dianne
Language:en_ca
Published: 2011
Subjects:
Online Access:http://hdl.handle.net/1807/31952
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spelling ndltd-TORONTO-oai-tspace.library.utoronto.ca-1807-319522013-04-19T19:56:25ZA Multifaceted Examination of the Central Processes Underlying Vestibular CompensationSweezie, Raquelvestibularneuron0317The vestibular system provides us with sensory information that is essential for maintaining balance and stability. When sensory input is lost due to unilateral vestibular damage (UVD), our ability to maintain stable gaze and posture becomes compromised. Over time, vestibular function is partially restored through a process known as vestibular compensation, which is associated with the rebalancing of activity in the vestibular nuclear complex (VNC) of the brainstem. However, the physiological mechanisms associated with vestibular compensation remain elusive. We addressed several different experimental objectives pertaining to plasticity and sensory adaptation associated with vestibular compensation. First, we demonstrated that systemic manipulation of γ-amino-butyric acid type B (GABAB) receptors altered the course of vestibular behavioural recovery within the first several hours after UVD. Second, we showed that immunohistochemical labeling of the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunit GluR4 was elevated in the VNC on the intact compared to lesioned side acutely following UVD. Third, we produced preliminary data suggesting that excitatory responses to vestibular nerve stimulation may be acutely potentiated by UVD on the intact side. Finally, we established that rapid sensory adaptation may increase the dynamic ranges of vestibular neurons and perhaps improve limited vestibular reflex function in the long term. Acutely following UVD, potentiation of vestibular nerve synapses appear to be associated with an increase in GluR4 subunit expression in the contralesional VNC. Also, such potentiation could be enhanced by acute modifications in pre-synaptic GABAB receptor activation. In the long term, and independent of these plastic changes, sensory adaptation may enable the vestibular system to overcome the persistent limitations imposed by UVD.Broussard, Dianne2011-112012-01-11T21:19:28ZNO_RESTRICTION2012-01-11T21:19:28Z2012-01-11Thesishttp://hdl.handle.net/1807/31952en_ca
collection NDLTD
language en_ca
sources NDLTD
topic vestibular
neuron
0317
spellingShingle vestibular
neuron
0317
Sweezie, Raquel
A Multifaceted Examination of the Central Processes Underlying Vestibular Compensation
description The vestibular system provides us with sensory information that is essential for maintaining balance and stability. When sensory input is lost due to unilateral vestibular damage (UVD), our ability to maintain stable gaze and posture becomes compromised. Over time, vestibular function is partially restored through a process known as vestibular compensation, which is associated with the rebalancing of activity in the vestibular nuclear complex (VNC) of the brainstem. However, the physiological mechanisms associated with vestibular compensation remain elusive. We addressed several different experimental objectives pertaining to plasticity and sensory adaptation associated with vestibular compensation. First, we demonstrated that systemic manipulation of γ-amino-butyric acid type B (GABAB) receptors altered the course of vestibular behavioural recovery within the first several hours after UVD. Second, we showed that immunohistochemical labeling of the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunit GluR4 was elevated in the VNC on the intact compared to lesioned side acutely following UVD. Third, we produced preliminary data suggesting that excitatory responses to vestibular nerve stimulation may be acutely potentiated by UVD on the intact side. Finally, we established that rapid sensory adaptation may increase the dynamic ranges of vestibular neurons and perhaps improve limited vestibular reflex function in the long term. Acutely following UVD, potentiation of vestibular nerve synapses appear to be associated with an increase in GluR4 subunit expression in the contralesional VNC. Also, such potentiation could be enhanced by acute modifications in pre-synaptic GABAB receptor activation. In the long term, and independent of these plastic changes, sensory adaptation may enable the vestibular system to overcome the persistent limitations imposed by UVD.
author2 Broussard, Dianne
author_facet Broussard, Dianne
Sweezie, Raquel
author Sweezie, Raquel
author_sort Sweezie, Raquel
title A Multifaceted Examination of the Central Processes Underlying Vestibular Compensation
title_short A Multifaceted Examination of the Central Processes Underlying Vestibular Compensation
title_full A Multifaceted Examination of the Central Processes Underlying Vestibular Compensation
title_fullStr A Multifaceted Examination of the Central Processes Underlying Vestibular Compensation
title_full_unstemmed A Multifaceted Examination of the Central Processes Underlying Vestibular Compensation
title_sort multifaceted examination of the central processes underlying vestibular compensation
publishDate 2011
url http://hdl.handle.net/1807/31952
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