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dc.contributor.advisorSteven R. Tannenbaum.en_US
dc.contributor.authorWright, Teresa Leah, 1970-en_US
dc.contributor.otherMassachusetts Institute of Technology. Division of Bioengineering and Environmental Health.en_US
dc.date.accessioned2005-08-23T18:06:05Z
dc.date.available2005-08-23T18:06:05Z
dc.date.copyright2001en_US
dc.date.issued2001en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/8182
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Division of Bioengineering and Environmental Health, 2001.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractThe overall aim of this project was to investigate various cellular responses and toxic effects of nitric oxide, NO' and in vitro and in vivo. Nitric oxide gives rise to a complex spectrum of reactive species in oxygenated solution. The complexity of nitric oxide's chemistry is recapitulated in its effects on cells. Exposure to nitric oxide can result in changes on many different levels in cells ranging from protein and DNA damage, to damage to organelles and changes in gene expression, and even in cell death. Many models to study nitric oxide have been developed and will be used to study various responses to nitric oxide and related species. Nitric oxide and peroxynitrite-induced cellular damage has been and continues to be studied extensively using in vitro systems. Two systems have been used in this project, a delivery system for NO' as well as a cell line, which produces NO'. A Silasticʾ membrane delivery system can be used to treat bacteria or cells to mimic in vivo exposure to nitric oxide. Mutations induced by nitric oxide in a set of Salmonella tester strains can be studied utilizing this delivery system. Activated RAW264.7 macrophage cells have been used as an in vitro model of nitric oxide production and cytotoxicity SJL/J mice bearing the transplantable lymphoma RcsX have been established as an in vivo model of nitric oxide production and toxicity.en_US
dc.description.abstract(cont.) This in vivo mouse model can be used to test results found in vitro. Specifically, the relationship between nitric oxide production and prostaglandin synthesis and glutathione homeostasis can be explored. Glutathione was found to be induced by nitric oxide production in this model, and this increase was due to increases in y-glutamylcysteinyl synthetase activity. This thesis studied both the regulatory and toxic effects of nitric oxide, both endogenously produced and from exogenous sources.en_US
dc.description.statementofresponsibilityby Teresa Leah Wright.en_US
dc.format.extent170 leavesen_US
dc.format.extent9263085 bytes
dc.format.extent9262842 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypeapplication/pdf
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/1721.1/7582
dc.subjectDivision of Bioengineering and Environmental Health.en_US
dc.titleNitric oxide : cellular effects in vitro and in vivoen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Bioengineering and Environmental Healthen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.identifier.oclc50047452en_US


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