Article ID Journal Published Year Pages File Type
5559731 Environmental Toxicology and Pharmacology 2017 6 Pages PDF
Abstract

•C3R significantly increased glucose uptake, which was associated with PM-GLUT4 expression in 3T3-L1 adipocytes.•C3R enhanced IRS-1 and Akt, as well as augmented activation of PI3K in the insulin signaling pathway.•C3R induced glucose uptake was inhibited only by the PI3K inhibitor.

In this study, the effect of cyanidin-3-rutinoside (C3R) on glucose uptake by 3T3-L1 adipocytes was studied. C3R significantly increased glucose uptake, which was associated with enhanced plasma membrane glucose transporter type 4 (PM-GLUT4) expression in 3T3-L1 adipocytes. The potentiating effect of C3R on glucose uptake and PM-GLUT4 expression was related to enhanced phosphorylation of insulin receptor substrate 1 (IRS-1) and Akt, as well as augmented activation of phosphatidylinositol-3-kinase (PI3K) in the insulin signaling pathway. C3R induced glucose uptake was inhibited only by the PI3K inhibitor, but not by an AMPK inhibitor in 3T3-L1 adipocytes. Therefore, C3R likely up-regulates glucose uptake and PM-GLUT4 expression in 3T3-L1 adipocytes by activating the PI3K/Akt pathways.

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