Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25899
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dc.contributor.authorDávalos-Salas, Mercedes-
dc.contributor.authorMariadason, John M-
dc.contributor.authorWatt, Matthew J-
dc.contributor.authorMontgomery, Magdalene K-
dc.date2020-06-11-
dc.date.accessioned2021-02-21T22:47:56Z-
dc.date.available2021-02-21T22:47:56Z-
dc.date.issued2020-08-
dc.identifier.citationBiochemical Pharmacology 2020; 178: 114091en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25899-
dc.description.abstractThe incidence of obesity and type 2 diabetes continues to rise across the globe necessitating the need to identify new therapeutic approaches to manage these diseases. In this review, we explore the potential for therapeutic interventions focussed on the intestinal epithelium, by targeting the role of this tissue in lipid uptake, lipid-mediated cross talk and lipid oxidation. We focus initially on ongoing strategies to manage obesity by targeting the essential role of the intestinal epithelium in lipid uptake, and in mediating tissue cross talk to regulate food intake. Subsequently, we explore a previously underestimated capacity of intestinal epithelial cells to oxidize fatty acids. In this context, we describe recent findings which have unveiled a key role for the peroxisome proliferator-activated receptor (PPAR) family of nuclear receptors and histone deacetylases (HDACs) in the regulation of lipid oxidation genes in enterocytes and how targeted genetic manipulation of these factors in enterocytes reduces weight gain, identifying intestinal PPARs and HDACs as potential therapeutic targets in the management of obesity.en
dc.language.isoeng
dc.subjectHDAC3en
dc.subjectIntestineen
dc.subjectLipid metabolismen
dc.subjectObesityen
dc.subjectPPARen
dc.titleMolecular regulators of lipid metabolism in the intestine - Underestimated therapeutic targets for obesity?en
dc.typeJournal Articleen
dc.identifier.journaltitleBiochemical Pharmacologyen
dc.identifier.affiliationOlivia Newton-John Cancer Research Instituteen
dc.identifier.affiliationLa Trobe University School of Cancer Medicine, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Physiology, Faculty of Medicine Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.doi10.1016/j.bcp.2020.114091en
dc.type.contentTexten
dc.identifier.pubmedid32535104
local.name.researcherMariadason, John M
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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