Document details

Loss of postprandial insulin clearance control by Insulin-degrading enzyme drives dysmetabolism traits

Author(s): 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

Date: 2021

Persistent ID: http://hdl.handle.net/10773/37382

Origin: RIA - Repositório Institucional da Universidade de Aveiro

Subject(s): Insulin clearance; Insulin-degrading enzyme; Genetic susceptibility; Hyperinsulinemia; Prediabetes; Hepatic steatosis


Description

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.

Document Type Journal article
Language English
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