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Fructose, Glucocorticoids and Adipose Tissue: Implications for the Metabolic Syndrome
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 3826617
Author(s) Legeza, Balázs; Marcolongo, Paola; Gamberucci, Alessandra; Varga, Viola; Bánhegyi, Gábor; Benedetti, Angiolo; Odermatt, Alex
Author(s) at UniBasel Odermatt, Alex
Year 2017
Title Fructose, Glucocorticoids and Adipose Tissue: Implications for the Metabolic Syndrome
Journal Nutrients
Volume 9
Number 5
Pages / Article-Number E426
Keywords adipogenesis, fructose, glucocorticoid, metabolic syndrome, obesity
Mesh terms 11-beta-Hydroxysteroid Dehydrogenase Type 1, metabolism; Adipose Tissue, physiology; Fructose, pharmacology; Gene Expression Regulation, Enzymologic, drug effects; Glucocorticoids, metabolism; Humans; Metabolic Syndrome, metabolism
Abstract The modern Western society lifestyle is characterized by a hyperenergetic, high sugar containing food intake. Sugar intake increased dramatically during the last few decades, due to the excessive consumption of high-sugar drinks and high-fructose corn syrup. Current evidence suggests that high fructose intake when combined with overeating and adiposity promotes adverse metabolic health effects including dyslipidemia, insulin resistance, type II diabetes, and inflammation. Similarly, elevated glucocorticoid levels, especially the enhanced generation of active glucocorticoids in the adipose tissue due to increased 11β-hydroxysteroid dehydrogenase 1 (11β-HSD1) activity, have been associated with metabolic diseases. Moreover, recent evidence suggests that fructose stimulates the 11β-HSD1-mediated glucocorticoid activation by enhancing the availability of its cofactor NADPH. In adipocytes, fructose was found to stimulate 11β-HSD1 expression and activity, thereby promoting the adipogenic effects of glucocorticoids. This article aims to highlight the interconnections between overwhelmed fructose metabolism, intracellular glucocorticoid activation in adipose tissue, and their metabolic effects on the progression of the metabolic syndrome.
Publisher MDPI AG
ISSN/ISBN 2072-6643
URL https://doi.org/10.3390/nu9050426
edoc-URL https://edoc.unibas.ch/63052/
Full Text on edoc No
Digital Object Identifier DOI 10.3390/nu9050426
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/28445389
ISI-Number WOS:000402054500004
Document type (ISI) Journal Article, Review
 
   

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