4.6 Article

[6]-Gingerol Affects Glucose Metabolism by Dual Regulation via the AMPK2-Mediated AS160-Rab5 Pathway and AMPK-Mediated Insulin Sensitizing Effects

Journal

JOURNAL OF CELLULAR BIOCHEMISTRY
Volume 116, Issue 7, Pages 1401-1410

Publisher

WILEY
DOI: 10.1002/jcb.25100

Keywords

AMPK; [6]-GINGEROL; DIABETES; INSULIN SENSITIZING; SIGNAL TRANSDUCTION

Funding

  1. Korean Government [NRF-2013R1A2A2A05004796]

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[6]-Gingerol has been used to control diabetes and dyslipidemia; however, its metabolic role is poorly understood. In this study, [6]-gingerol increased adenosine monophosphate (AMP)-activated protein kinase (AMPK) phosphorylation in mouse skeletal muscle C2C12 cells. Stimulation of glucose uptake by [6]-gingerol was dependent on AMPK2. Moreover, both Inhibition and knockdown of AMPK2 blocked [6]-gingerol-induced glucose uptake. [6]-Gingerol significantly decreased the activity of protein phosphatase 2A (PP2A). Inhibition of PP2A activity with okadaic acid enhanced the phosphorylation of AMPK2. Moreover, the interaction between AMPK2 and PP2A was increased by [6]-gingerol, suggesting that PP2A mediates the effect of [6]-gingerol on AMPK phosphorylation. In addition, [6]-gingerol increased the phosphorylation of Akt-substrate 160 (AS160), which is a Rab GTPase-activating protein. Inhibition of AMPK2 blocked [6]-gingerol-induced AS160 phosphorylation. [6]-gingerol increased the Rab5, and AMPK2 knockdown blocked [6]-gingerol-induced expression of Rab5, indicating AMPK play as an upstream of Rab5. It also increased glucose transporter 4 (GLUT4) mRNA and protein expression and stimulated GLUT4 translocation. Furthermore, insulin-mediated glucose uptake and Akt phosphorylation were further potentiated by [6]-gingerol treatment. This potentiation was not observed in the presence of AMPK inhibitor compound C. In summary, our results suggest that [6]-gingerol plays an important role in glucose metabolism via the AMPK2-mediated AS160-Rab5 pathway and through potentiation of insulin-mediated glucose regulation. J. Cell. Biochem. 116: 1401-1410, 2015. (c) 2015 Wiley Periodicals, Inc.

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