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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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 |
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vestibular neuron 0317 |
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vestibular neuron 0317 Sweezie, Raquel A Multifaceted Examination of the Central Processes Underlying Vestibular Compensation |
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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 |
work_keys_str_mv |
AT sweezieraquel amultifacetedexaminationofthecentralprocessesunderlyingvestibularcompensation AT sweezieraquel multifacetedexaminationofthecentralprocessesunderlyingvestibularcompensation |
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1716582153142140928 |