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dc.contributor.authorWeltman, Martin D. (Martin David)
dc.date.accessioned2022-03-16T22:40:03Z
dc.date.available2022-03-16T22:40:03Z
dc.date.issued1998en
dc.identifier.urihttps://hdl.handle.net/2123/27739
dc.descriptionIncludes publication
dc.description.abstractThe relevant literature concerning nonalcoholic steatohepatitis (NASH), the morphologically similar condition of alcoholic liver disease (ALD), and the hepatic cytochromes P450 (P450 or CYP) was reviewed with particular emphasis on CYP2E1. CYP2E1 is induced in ALD. It plays an important role in the pathogenesis of this condition by generating reactive oxygen species (ROS). In turn, ROS produce lipid peroxidation, which contributes to the cellular injury in ALD. CYP2E1 is constitutively expressed in acinar zone 3. The early lesions observed in both ALD and NASH are most pronounced in the same acinar region of the liver. Since NASH and ALD have similar histological appearances, the possibility that CYP2E1 may play a significant role in the pathogenesis of NASH was considered. One of the limitations in evaluating the pathogenesis of NASH has been the absence of an appropriate animal model.en
dc.language.isoenen
dc.rightsThe author retains copyright of this thesis
dc.subjectFatty liver -- Etiologyen
dc.subjectHepatitis -- Etiologyen
dc.subjectCytochrome P-450 CYP2E1en
dc.titlePathogenesis of nonalcoholic steatohohepatitis [sic] : the role of CYP2E1en
dc.typeThesis
dc.type.thesisDoctor of Philosophyen
dc.rights.otherThe author retains copyright of this thesis. It may only be used for the purposes of research and study. It must not be used for any other purposes and may not be transmitted or shared with others without prior permission.en
usyd.facultyFaculty of Medicineen
usyd.departmentDepartment of Medicineen
usyd.degreeDoctor of Philosophy Ph.D.en
usyd.awardinginstThe University of Sydneyen
usyd.include.pubYesen


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