期刊
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
卷 1800, 期 3, 页码 359-366出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbagen.2009.12.002
关键词
3 beta-Taraxerol; Mangifera indica; Glycogen synthesis; Glucose uptake; 3T3-L1 adipocytes; GSK3 beta; PI3K
Background: The present study focuses on identifying and developing an anti-diabetic molecule from plant sources that would effectively combat insulin resistance through proper channeling of glucose metabolism involving glucose transport and storage. Methods: Insulin-stimulated glucose uptake formed the basis for isolation of a bioactive molecule through column chromatography followed by its characterization using NMR and mass spectroscopic analysis. Mechanism of glucose transport and storage was evaluated based on the expression profiling of signaling molecules involved in the process. Results: The study reports (i) the isolation of a bioactive compound 3 beta-taraxerol from the ethyl acetate extract (EAE) of the leaves of Mangifera indica (ii) the bioactive compound exhibited insulin-stimulated glucose uptake through translocation and activation of the glucose transporter (GLUT4) in an IRTK and PI3K dependent fashion. (iii) the fate of glucose following insulin-stimulated glucose uptake was ascertained through glycogen synthesis assay that involved the activation of PKB and suppression of GSK3 beta. General significance: This study demonstrates the dual activity of 3 beta-taraxerol and the ethyl acetate extract of Mangifera indica as a glucose transport activator and stimulator of glycogen synthesis. 3 beta-taraxerol can be validated as a potent candidate for managing the hyperglycemic state. (C) 2009 Elsevier B.V. All rights reserved.
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