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dc.contributor.advisorKay Tye and Cody Siciliano.en_US
dc.contributor.authorLee, Jennifer J.,M. Eng.Massachusetts Institute of Technology.en_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science.en_US
dc.date.accessioned2019-12-05T18:07:07Z
dc.date.available2019-12-05T18:07:07Z
dc.date.copyright2019en_US
dc.date.issued2019en_US
dc.identifier.urihttps://hdl.handle.net/1721.1/123168
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionThesis: M. Eng. in Computer Science and Molecular Biology, Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2019en_US
dc.descriptionCataloged from student-submitted PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 33-34).en_US
dc.description.abstractAlcohol addiction is a prevalent and complex disorder, with neural underpinnings that warrant further investigation. We devised a novel Pavlovian conditioning task whereby compulsive alcohol drinking behaviors are induced in a mouse model. This model identified individual variations in alcohol intake and compulsive drinking between animals and across time, and showed that medial prefrontal cortex-dorsal periaqueductal gray (mPFC-dPAG) projectors are involved in the encoding of alcohol related stimuli. To elucidate the role of mPFC-dPAG neurons in compulsive alcohol drinking, we first created a transparent signalprocessing method to reliably and accurately detect transients in neuronal traces. This pipeline limits data modification as much as possible, and employs a simple moving average filter and sliding z-score threshold to identify likely events. We also built a transcriptional profile of the mPFC-dPAG neurons via translating ribosome affinity purification (TRAP) followed by RNA sequencing technology, and validated our findings via fluorescent in situ hybridization. Finally, we turned to the online BXD database to build prediction models capable of classifying mice as "low drinkers" or "high drinkers" based on consensus genotypes. Together, these approaches reveal the behavioral and neural characteristics that facilitate the development of alcohol-induced compulsive behaviors.en_US
dc.description.statementofresponsibilityby Jennifer J. Lee.en_US
dc.format.extent34 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectElectrical Engineering and Computer Science.en_US
dc.titlePredicting compulsive alcohol drinkingen_US
dc.typeThesisen_US
dc.description.degreeM. Eng. in Computer Science and Molecular Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.identifier.oclc1129384832en_US
dc.description.collectionM.Eng.inComputerScienceandMolecularBiology Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Scienceen_US
dspace.imported2019-12-05T18:07:06Zen_US
mit.thesis.degreeMasteren_US
mit.thesis.departmentEECSen_US


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