Dystonia is a movement disorder characterized by patterned, repetitive, and sustained muscle contractions that cause ineffective and often painful movements. The overall goal of this project was to understand the physiological mechanisms of dystonia in a rodent model as a basis for developing innovative treatments for secondary dystonias. The first half of the project was focused at developing essential techniques for systematically investigating the movement disorder in these animals. For achieving this, an innovative, multi-faceted approach was pursued starting with electromyographic (EMG) analysis for animal model validation, gait analysis for dystonia quantification, and development of a novel stereotaxic apparatus for recording brain activity during awake conditions. The later half of the project was focused on understanding how brain circuitry produces abnormal motor control in dystonia. Single and multi-unit neuronal activity was collected from individual basal ganglia nuclei along with EMG recordings to characterize the abnormal patterns of firing in dystonic animals and determine how neurons within individual nuclei communicate in dystonia, respectively. The findings of the current project have lead to new insights into the pathophysiology and treatment of secondary kernicteric dystonia and other secondary dystonia in humans.
| Identifer | oai:union.ndltd.org:vcu.edu/oai:scholarscompass.vcu.edu:etd-1092 |
| Date | 23 April 2010 |
| Creators | Chaniary, Kunal |
| Publisher | VCU Scholars Compass |
| Source Sets | Virginia Commonwealth University |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | Theses and Dissertations |
| Rights | © The Author |
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