Alexander Disease and Potential Treatment through the Nrf2-ARE Pathway

dc.contributor.authorSmall, Alexandra Joanne
dc.date.accessioned2014-09-23T17:38:33Z
dc.date.available2014-09-23T17:38:33Z
dc.date.issued2014-05
dc.description35 pages. A thesis presented to the Department of Biology and the Clark Honors College of the University of Oregon in partial fulfillment of the requirements for degree of Bachelor of Science, Spring 2014.en_US
dc.description.abstractNeurological diseases have high prevalence globally and most are untreatable. Neurodegenerative diseases like Alzheimer's disease (AD) and Parkinson's disease (PO) are highly common especially with a growing elderly population. Alexander disease (ALX) is a rare neurodegenerative brain disease that typically affects infants, but has paralleling characteristics with AD, PD and Amyotrophic Lateral Sclerosis (ALS) including oxidative stress and neuronal degeneration. As a consequence ALX is much less researched. Using the large volume of research that has been done on AD, PO and ALS, this paper explores the possibility of using cellular antioxidant pathways, specifically the Nrf2-ARE pathway, to treat ALX. By utilizing the different experimental approaches taken in animal and cellular models of AD, PO, and ALS it is proposed that further research regarding the Nrf2-ARE pathway in ALX models is needed for its use for potential treatment.en_US
dc.identifier.urihttps://hdl.handle.net/1794/18303
dc.language.isoen_USen_US
dc.publisherUniversity of Oregonen_US
dc.relation.ispartofseriesUniversity of Oregon theses, Dept. of Biology, Honors College, B.S., 2014;
dc.rightsAll Rights Reserved.en_US
dc.subjectAlexander Diseaseen_US
dc.subjectBrain diseasesen_US
dc.subjectOxidative stressen_US
dc.subjectNrf2-ARE Pathwayen_US
dc.subjectLeukodystrophyen_US
dc.titleAlexander Disease and Potential Treatment through the Nrf2-ARE Pathwayen_US
dc.typeThesis / Dissertationen_US

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