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Steviol Glycosides Modulate Glucose Transport in Different Cell Types
Author(s) -
Benedetta Rizzo,
Laura Zambonin,
Cristina Angeloni,
Emanuela Leoncini,
Francesco Vieceli Dalla Sega,
Cecilia Prata,
Diana Fiorentini,
Silvana Hrelia
Publication year - 2013
Publication title -
oxidative medicine and cellular longevity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.494
H-Index - 93
eISSN - 1942-0900
pISSN - 1942-0994
DOI - 10.1155/2013/348169
Subject(s) - steviol , stevia rebaudiana , pi3k/akt/mtor pathway , protein kinase b , stevioside , glycoside , pharmacology , insulin , chemistry , insulin receptor , biochemistry , biology , phosphorylation , medicine , signal transduction , endocrinology , insulin resistance , food science , stereochemistry , alternative medicine , pathology
Extracts from Stevia rebaudiana Bertoni, a plant native to Central and South America, have been used as a sweetener since ancient times. Currently, Stevia extracts are largely used as a noncaloric high-potency biosweetener alternative to sugar, due to the growing incidence of type 2 diabetes mellitus, obesity, and metabolic disorders worldwide. Despite the large number of studies on Stevia and steviol glycosides in vivo , little is reported concerning the cellular and molecular mechanisms underpinning the beneficial effects on human health. The effect of four commercial Stevia extracts on glucose transport activity was evaluated in HL-60 human leukaemia and in SH-SY5Y human neuroblastoma cells. The extracts were able to enhance glucose uptake in both cellular lines, as efficiently as insulin. Our data suggest that steviol glycosides could act by modulating GLUT translocation through the PI3K/Akt pathway since treatments with both insulin and Stevia extracts increased the phosphorylation of PI3K and Akt. Furthermore, Stevia extracts were able to revert the effect of the reduction of glucose uptake caused by methylglyoxal, an inhibitor of the insulin receptor/PI3K/Akt pathway. These results corroborate the hypothesis that Stevia extracts could mimic insulin effects modulating PI3K/Akt pathway.

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