{"id":{"repo_id":"vcu","oai_identifier":"oai:scholarscompass.vcu.edu:etd-1092"},"canonical_url":"https://search.dev.ndltd.org/etd/vcu/oai:scholarscompass.vcu.edu:etd-1092","repository":{"repo_id":"vcu","name":"Virginia Commonwealth University","base_url":"https://scholarscompass.vcu.edu/do/oai/"},"display":{"title":"Electrophysiological Analysis in an Animal Model of Dystonia","abstract":"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.","abstract_html":"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.","abstract_has_math":false,"creators":["Chaniary, Kunal"],"institution":null,"degree_name":"Doctor of Philosophy","degree_level":"Dissertation","degree_discipline":"Biomedical Engineering","degree_department":null,"school":null,"contributors":["Paul Wetzel"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2010,"date_issued":"2010-04-23T07:00:00Z","date_published":"2010-04-23T07:00:00Z","updated_at":"2026-07-24T05:53:18Z","subjects":["dystonia","electrophysiology","Biomedical Engineering and Bioengineering","Engineering"],"languages":[],"rights":["© The Author"],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["https://scholarscompass.vcu.edu/etd/93"],"render_values":[{"text":"https://scholarscompass.vcu.edu/etd/93","href":"https://scholarscompass.vcu.edu/etd/93","code":true}]}]},"links":{"outbound_url":"https://doi.org/10.25772/49TW-2225","outbound_label":"DOI","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Paul Wetzel"]},{"key":"dc:creator","label":"Author","values":["Chaniary, Kunal"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2015-05-14T07:00:00Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biomedical Engineering"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Doctor of Philosophy"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["dystonia","electrophysiology","Biomedical Engineering and Bioengineering","Engineering"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["© The Author"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://doi.org/10.25772/49TW-2225","https://scholarscompass.vcu.edu/etd/93"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["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."]},{"key":"dc:title","label":"Title","values":["Electrophysiological Analysis in an Animal Model of Dystonia"]}]}],"canonical_facts":{"dc:contributor":["Paul Wetzel"],"dc:creator":["Chaniary, Kunal"],"dc:date.available":["2015-05-14T07:00:00Z"],"dc:description.abstract":["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."],"dc:identifier":["https://doi.org/10.25772/49TW-2225","https://scholarscompass.vcu.edu/etd/93"],"dc:rights":["© The Author"],"dc:subject":["dystonia","electrophysiology","Biomedical Engineering and Bioengineering","Engineering"],"dc:title":["Electrophysiological Analysis in an Animal Model of Dystonia"],"thesis:degree_discipline":["Biomedical Engineering"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Doctor of Philosophy"]},"updated_at":"2026-07-24T05:53:18Z"}