Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/23509
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dc.contributor.authorYap, Yann W-
dc.contributor.authorRusu, Patricia M-
dc.contributor.authorChan, Andrea Y-
dc.contributor.authorFam, Barbara C-
dc.contributor.authorJungmann, Andreas-
dc.contributor.authorSolon-Biet, Samantha M-
dc.contributor.authorBarlow, Christopher K-
dc.contributor.authorCreek, Darren J-
dc.contributor.authorHuang, Cheng-
dc.contributor.authorSchittenhelm, Ralf B-
dc.contributor.authorMorgan, Bruce-
dc.contributor.authorSchmoll, Dieter-
dc.contributor.authorKiens, Bente-
dc.contributor.authorPiper, Matthew D W-
dc.contributor.authorHeikenwälder, Mathias-
dc.contributor.authorSimpson, Stephen J-
dc.contributor.authorBröer, Stefan-
dc.contributor.authorAndrikopoulos, Sofianos-
dc.contributor.authorMüller, Oliver J-
dc.contributor.authorRose, Adam J-
dc.date2020-06-09-
dc.date.accessioned2020-06-15T06:54:47Z-
dc.date.available2020-06-15T06:54:47Z-
dc.date.issued2020-06-09-
dc.identifier.citationNature Communications 2020; 11(1): 2894-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/23509-
dc.description.abstractDietary protein dilution (DPD) promotes metabolic-remodelling and -health but the precise nutritional components driving this response remain elusive. Here, by mimicking amino acid (AA) supply from a casein-based diet, we demonstrate that restriction of dietary essential AA (EAA), but not non-EAA, drives the systemic metabolic response to total AA deprivation; independent from dietary carbohydrate supply. Furthermore, systemic deprivation of threonine and tryptophan, independent of total AA supply, are both adequate and necessary to confer the systemic metabolic response to both diet, and genetic AA-transport loss, driven AA restriction. Dietary threonine restriction (DTR) retards the development of obesity-associated metabolic dysfunction. Liver-derived fibroblast growth factor 21 is required for the metabolic remodelling with DTR. Strikingly, hepatocyte-selective establishment of threonine biosynthetic capacity reverses the systemic metabolic response to DTR. Taken together, our studies of mice demonstrate that the restriction of EAA are sufficient and necessary to confer the systemic metabolic effects of DPD.-
dc.language.isoeng-
dc.titleRestriction of essential amino acids dictates the systemic metabolic response to dietary protein dilution.-
dc.typeJournal Articleen
dc.identifier.journaltitleNature Communications-
dc.identifier.affiliationMonash Institute of Pharmaceutical Sciences, Monash University, Melbourne, VIC, 3052, Australiaen
dc.identifier.affiliationDepartment of Biochemistry and Molecular Biology, Metabolism, Diabetes and Obesity Program, Biomedicine Discovery Institute, Monash University, Clayton, VIC, 3800, Australiaen
dc.identifier.affiliationBiomedical Proteomics and Metabolomics Facility and the Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC, 3800, Australiaen
dc.identifier.affiliationCharles Perkins Centre, School of Life and Environmental Sciences, University of Sydney, Sydney, NSW, Australiaen
dc.identifier.affiliationDivision of Chronic Inflammation and Cancer, German Cancer Research Center, 69120, Heidelberg, Germanyen
dc.identifier.affiliationSanofi-Aventis Deutschland GmbH, Industriepark Hoechst, Frankfurt am Main, 65926, Germanyen
dc.identifier.affiliationInstitute for Biochemistry, Centre for Human and Molecular Biology (ZHMB), Saarland University, 66123, Saarbrücken, Germanyen
dc.identifier.affiliationSchool of Biological Sciences, School of Life and Environmental Sciences, Monash University, Clayton, VIC, 3800, Australiaen
dc.identifier.affiliationDepartment of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationResearch School of Biology, Australian National University, Canberra, ACT, 0200, Australiaen
dc.identifier.affiliationGerman Center for Cardiovascular Research (DZHK), Partner sites Kiel and Heidelberg, Germanyen
dc.identifier.affiliationDepartment of Internal Medicine III, University of Kiel, Kiel, Germanyen
dc.identifier.affiliationDepartment of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germanyen
dc.identifier.affiliationSection of Molecular Physiology, Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, 2100, Copenhagen, Denmark..-
dc.identifier.doi10.1038/s41467-020-16568-z-
dc.type.contentTexten
dc.identifier.orcid0000-0001-7210-1976-
dc.identifier.orcid0000-0003-0608-958X-
dc.identifier.orcid0000-0002-4575-1233-
dc.identifier.orcid0000-0001-8738-1878-
dc.identifier.orcid0000-0001-9393-1071-
dc.identifier.orcid0000-0001-5705-5625-
dc.identifier.orcid0000-0003-0256-7687-
dc.identifier.orcid0000-0002-8040-1634-
dc.identifier.orcid0000-0001-8223-2638-
dc.identifier.orcid0000-0001-9132-8244-
dc.identifier.pubmedid32518324-
dc.type.austinJournal Article-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
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