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Borges, Diego O.; Patarrão, Rita S.; Ribeiro, Rogério T.; de Oliveira, Rita Machado; Duarte, Nádia; Belew, Getachew Debas; Martins, Madalena; Andrade, Rita; Costa, João; Correia, Isabel; Boavida, José Manuel; Duarte, Rui; Gardete-Correia, Luís; Medina, José Luís; Raposo, João F.; Jones, John G.; Penha-Gonçalves, Carlos; Macedo, M. Paula
Metabolism, clinical and experimental, 20/May , Letnik: 118Journal Article
Systemic insulin availability is determined by a balance between beta-cell secretion capacity and insulin clearance (IC). Insulin-degrading enzyme (IDE) is involved in the intracellular mechanisms underlying IC. The liver is a major player in IC control yet the role of hepatic IDE in glucose and lipid homeostasis remains unexplored. We hypothesized that IDE governs postprandial IC and hepatic IDE dysfunction amplifies dysmetabolic responses and prediabetes traits such as hepatic steatosis. In a European/Portuguese population-based cohort, IDE SNPs were strongly associated with postprandial IC in normoglycemic men but to a considerably lesser extent in women or in subjects with prediabetes. Liver-specific knockout-mice (LS-IDE KO) under normal chow diet (NCD), showed reduced postprandial IC with glucose intolerance and under high fat diet (HFD) were more susceptible to hepatic steatosis than control mice. This suggests that regulation of IC by IDE contributes to liver metabolic resilience. In agreement, LS-IDE KO hepatocytes revealed reduction of Glut2 expression levels with consequent impairment of glucose uptake and upregulation of CD36, a major hepatic free fatty acid transporter. Together these findings provide strong evidence that dysfunctional IC due to abnormal IDE regulation directly impairs postprandial hepatic glucose disposal and increases susceptibility to dysmetabolic conditions in the setting of Western diet/lifestyle. Display omitted •IDE polymorphisms strongly associate with postprandial IC in NGT men.•IDE polymorphisms association with IC is weaken in women and prediabetes.•Liver-specific IDE KO display reduced postprandial IC.•Liver-specific IDE KO display glucose intolerance correlated with reduced glut2.•Liver-specific IDE KO exacerbates hepatic steatosis induced by high fat diet.
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