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The db mouse as a model for steatohepatitis

Includes bibliographical references.

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Bibliographic Details
Main Author: Sutherland, Jason Robert
Other Authors: Hall, Pauline de la Motte
Format: Thesis
Language:English
Published: Division of Anatomical Pathology 2014
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access_status_str Open Access
author Sutherland, Jason Robert
author2 Hall, Pauline de la Motte
author_browse Hall, Pauline de la Motte
Sutherland, Jason Robert
author_facet Hall, Pauline de la Motte
Sutherland, Jason Robert
author_sort Sutherland, Jason Robert
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/7434
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:34:33.896Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Division of Anatomical Pathology
publisherStr Division of Anatomical Pathology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/7434 The db mouse as a model for steatohepatitis Sutherland, Jason Robert Hall, Pauline de la Motte Marais, David Anatomical Pathology Includes bibliographical references. Fatty liver disease is a collective phrase for a spectrum of diseases characterised by increased liver fat content. It ranges from fatty infiltration of the liver to an inflammatory condition, steatohepatitis, which may lead onto cirrhosis. Although not associated with alcohol consumption, non-alcoholic steatohepatitis (NASH) has strong associations with obesity, diabetes and dyslipidaemia. Overlapping pathological mechanisms may be involved. The course of the disease will remain unpredictable, and specific treatment will only be able to be instituted once the pathogenesis is fully understood. This thesis reviews current understanding of the pathogenesis and explores the suitability of a recently defined obese diabetic mouse model for its value as a model in the heterozygous and homozygous states. Observations revealed that the db/wt phenotype has a larger mass than the wt/wt and responds with hyperglycaemia. Lipid accumulation occurs in this model when alcohol is administered and lipid peroxidation occurs but histological changes of steatosis and steatohepatitis do not occur. The db/db model is phenotypically distinguished by a large amount of fat storage, diabetes and macrovesicular steatosis that has more lipid peroxidation but no steatohepatitis even when alcohol further increases lipid peroxidation. The model, as explored, did not reveal steatohepatitis either alone, or with alcohol as a single additional stressor, but both the db/wt and db/db mouse model could be further investigated to explore whether additional stressors could induce steaotohepatitis in this model. 2014-09-12T07:04:44Z 2014-09-12T07:04:44Z 2006 Master Thesis Masters MSc http://hdl.handle.net/11427/7434 eng application/pdf Division of Anatomical Pathology Faculty of Health Sciences University of Cape Town
spellingShingle Anatomical Pathology
Sutherland, Jason Robert
The db mouse as a model for steatohepatitis
thesis_degree_str Master's
title The db mouse as a model for steatohepatitis
title_full The db mouse as a model for steatohepatitis
title_fullStr The db mouse as a model for steatohepatitis
title_full_unstemmed The db mouse as a model for steatohepatitis
title_short The db mouse as a model for steatohepatitis
title_sort db mouse as a model for steatohepatitis
topic Anatomical Pathology
url http://hdl.handle.net/11427/7434
work_keys_str_mv AT sutherlandjasonrobert thedbmouseasamodelforsteatohepatitis
AT sutherlandjasonrobert dbmouseasamodelforsteatohepatitis