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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
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
dc.publisherSAGE journalsen
dc.relation.ispartofInternational Journal of Tryptophan Researchen
dc.rightsCreative Commons Attribution-NonCommercial 4.0en
dc.subjectNonalcoholic steatohepatitisen
dc.subjectdysbiosisen
dc.subjectinflammationen
dc.subjectintestinal microbiomeen
dc.subjecttryptophanen
dc.titleIntestinal Dysbiosis, the Tryptophan Pathway and Nonalcoholic Steatohepatitis.en
dc.typeArticleen
dc.subject.asrc0304 Medicinal and Biomolecular Chemistryen
dc.identifier.doi10.1177/11786469211070533
dc.type.pubtypePublisher's versionen
usyd.facultySeS faculties schools::Faculty of Medicine and Health::The University of Sydney School of Pharmacyen
workflow.metadata.onlyNoen


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