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Tea catechins modulate the glucose transport system in 3T3-L1 adipocytes

Authors :
Yukiko Aoki
Itsuko Fukuda
Takashi Furuyashiki
Hitoshi Ashida
Manabu Ueda
Kayo Yamada
Iwao Sakane
Ken-ichi Yoshida
Source :
Food & Function. 1:167
Publication Year :
2010
Publisher :
Royal Society of Chemistry (RSC), 2010.

Abstract

In this study, we investigated the effects of tea catechins on the translocation of glucose transporter (GLUT) 4 in 3T3-L1 adipocytes. We found that the ethyl acetate fraction of green tea extract, containing abundant catechins, most decreased insulin-induced glucose uptake activity in 3T3-L1 cells. When the cells were treated with 50 μM catechins in the absence or presence of insulin for 30 min, nongallate-type catechins increased glucose uptake activity without insulin, whereas gallate-type catechins decreased insulin-induced glucose uptake activity. (-)-Epicatechin (EC) and (-)-epigallocatechin (EGC), nongallate-type catechins, increased glucose uptake activity in the dose- and time-dependent manner, whereas (-)-catechin 3-gallate (Cg) and (-)-epigallocatechin 3-gallate (EGCg), gallate-type catechins, decreased insulin-induced glucose uptake activity in the dose- and time-dependent manner. When the cells were treated with 50 μM catechins for 30 min, EC and EGC promoted GLUT4 translocation, whereas Cg and EGCg decreased the insulin-induced translocation in the cells. EC and EGC increased phosphorylation of PKCλ/ζ without phosphorylation of insulin receptor (IR) and Akt. Wortmannin and LY294002, inhibitors for phosphatidylinositol 3'-kinase (PI3K), decreased EC- and EGC-induced glucose uptake activity in the cells. Cg and EGCg decreased phosphorylation of PKCλ/ζ in the presence of insulin without affecting insulin-induced phosphorylation of IR, and Akt. Therefore, EC and EGC promote the translocation of GLUT4 through activation of PI3K, and Cg and EGCg inhibit insulin-induced translocation of GLUT4 by the insulin signaling pathway in 3T3-L1 cells.

Details

ISSN :
2042650X and 20426496
Volume :
1
Database :
OpenAIRE
Journal :
Food & Function
Accession number :
edsair.doi.dedup.....48a69a54dcdf3b39662c2d0bc6a11c6a
Full Text :
https://doi.org/10.1039/c0fo00105h