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dc.contributor.authorChen, Jiezhong
dc.contributor.authorVitetta, Luis
dc.contributor.authorHenson, Jeremy D
dc.contributor.authorHall, Sean
dc.date.accessioned2022-08-24T05:00:07Z
dc.date.available2022-08-24T05:00:07Z
dc.date.issued2022en_AU
dc.identifier.urihttps://hdl.handle.net/2123/29458
dc.description.abstractNon-alcoholic fatty liver disease (NAFLD) progresses from simple steatosis to steatohepatitis (NASH), which may then progress to the development of cirrhosis and hepatocarcinoma. NASH is characterized by both steatosis and inflammation. Control of inflammation in NASH is a key step for the prevention of disease progression to severe sequalae. Intestinal dysbiosis has been recognized to be an important causal factor in the pathogenesis of NASH, involving both the accumulation of lipids and aggravation of inflammation. The effects of gut dysbiosis are mediated by adverse shifts of various intestinal commensal bacterial genera and their associated metabolites such as butyrate, tryptophan, and bile acids. In this review, we focus on the roles of tryptophan and its metabolites in NASH in association with intestinal dysbiosis and discuss possible therapeutic implications.en_AU
dc.publisherSAGE journalsen_AU
dc.relation.ispartofInternational Journal of Tryptophan Researchen_AU
dc.rightsCreative Commons Attribution-NonCommercial 4.0en_AU
dc.subjectNonalcoholic steatohepatitisen_AU
dc.subjectdysbiosisen_AU
dc.subjectinflammationen_AU
dc.subjectintestinal microbiomeen_AU
dc.subjecttryptophanen_AU
dc.titleIntestinal Dysbiosis, the Tryptophan Pathway and Nonalcoholic Steatohepatitis.en_AU
dc.typeArticleen_AU
dc.subject.asrc0304 Medicinal and Biomolecular Chemistryen_AU
dc.identifier.doi10.1177/11786469211070533
dc.type.pubtypePublisher's versionen_AU
usyd.facultySeS faculties schools::Faculty of Medicine and Health::The University of Sydney School of Pharmacyen_AU
workflow.metadata.onlyNoen_AU


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