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Lowering apolipoprotein CIII protects against high-fat diet-induced metabolic derangements
Rolf Luft Research Center for Diabetes and Endocrinology, Karolinska Institutet, Karolinska University Hospital L1, Stockholm, Sweden.
Rolf Luft Research Center for Diabetes and Endocrinology, Karolinska Institutet, Karolinska University Hospital L1, Stockholm, Sweden.
Rolf Luft Research Center for Diabetes and Endocrinology, Karolinska Institutet, Karolinska University Hospital L1, Stockholm, Sweden.
Rolf Luft Research Center for Diabetes and Endocrinology, Karolinska Institutet, Karolinska University Hospital L1, Stockholm, Sweden.
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2021 (English)In: Science Advances, E-ISSN 2375-2548, Vol. 7, no 11, article id eabc2931Article in journal (Refereed) Published
Abstract [en]

Increased levels of apolipoprotein CIII (apoCIII), a key regulator of lipid metabolism, result in obesity-related metabolic derangements. We investigated mechanistically whether lowering or preventing high-fat diet (HFD)-induced increase in apoCIII protects against the detrimental metabolic consequences. Mice, first fed HFD for 10 weeks and thereafter also given an antisense (ASO) to lower apoCIII, already showed reduced levels of apoCIII and metabolic improvements after 4 weeks, despite maintained obesity. Prolonged ASO treatment reversed the metabolic phenotype due to increased lipase activity and receptor-mediated hepatic uptake of lipids. Fatty acids were transferred to the ketogenic pathway, and ketones were used in brown adipose tissue (BAT). This resulted in no fat accumulation and preserved morphology and function of liver and BAT. If ASO treatment started simultaneously with the HFD, mice remained lean and metabolically healthy. Thus, lowering apoCIII protects against and reverses the HFD-induced metabolic phenotype by promoting physiological insulin sensitivity.

Place, publisher, year, edition, pages
American Association for the Advancement of Science , 2021. Vol. 7, no 11, article id eabc2931
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Endocrinology and Diabetes
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URN: urn:nbn:se:umu:diva-182040DOI: 10.1126/sciadv.abc2931ISI: 000628616300004PubMedID: 33712458Scopus ID: 2-s2.0-85102911775OAI: oai:DiVA.org:umu-182040DiVA, id: diva2:1545164
Available from: 2021-04-19 Created: 2021-04-19 Last updated: 2023-09-05Bibliographically approved

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Ericsson, MadeleneLandfors, FredrikNilsson, Stefan K.

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