3β-taraxerol of Mangifera indica, a PI3K dependent dual activator of glucose transport and glycogen synthesis in 3T3-L1 adipocytes
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. Insulin-stimulated glucose uptake formed the basis for isolat...
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Published in | Biochimica et biophysica acta. General subjects Vol. 1800; no. 3; pp. 359 - 366 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.03.2010
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ISSN | 0304-4165 1872-8006 |
DOI | 10.1016/j.bbagen.2009.12.002 |
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Abstract | 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.
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.
The study reports (i) the isolation of a bioactive compound 3β-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 GSK3β.
This study demonstrates the dual activity of 3β-taraxerol and the ethyl acetate extract of
Mangifera indica as a glucose transport activator and stimulator of glycogen synthesis. 3β-taraxerol can be validated as a potent candidate for managing the hyperglycemic state. |
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AbstractList | 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.
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.
The study reports (i) the isolation of a bioactive compound 3β-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 GSK3β.
This study demonstrates the dual activity of 3β-taraxerol and the ethyl acetate extract of
Mangifera indica as a glucose transport activator and stimulator of glycogen synthesis. 3β-taraxerol can be validated as a potent candidate for managing the hyperglycemic state. |
Author | Anand, Singaravel Velmurugan, Devadasan Nithya, Nirmal Muthusamy, Velusamy Shanmuganathan Sangeetha, Kadapakkam Nandabalan Balakrishnan, Arun Lakshmi, Baddireddi Subhadra Sujatha, Sundaresan |
Author_xml | – sequence: 1 givenname: Kadapakkam Nandabalan surname: Sangeetha fullname: Sangeetha, Kadapakkam Nandabalan organization: Centre for Biotechnology, Anna University, India – sequence: 2 givenname: Sundaresan surname: Sujatha fullname: Sujatha, Sundaresan organization: Centre for Biotechnology, Anna University, India – sequence: 3 givenname: Velusamy Shanmuganathan surname: Muthusamy fullname: Muthusamy, Velusamy Shanmuganathan organization: Centre for Biotechnology, Anna University, India – sequence: 4 givenname: Singaravel surname: Anand fullname: Anand, Singaravel organization: Centre for Biotechnology, Anna University, India – sequence: 5 givenname: Nirmal surname: Nithya fullname: Nithya, Nirmal organization: Centre of Advanced study in Crystallography and Biophysics, University of Madras, India – sequence: 6 givenname: Devadasan surname: Velmurugan fullname: Velmurugan, Devadasan organization: Centre of Advanced study in Crystallography and Biophysics, University of Madras, India – sequence: 7 givenname: Arun surname: Balakrishnan fullname: Balakrishnan, Arun organization: Department of Pharmacology, Nicholas Piramal Research Centre, India – sequence: 8 givenname: Baddireddi Subhadra surname: Lakshmi fullname: Lakshmi, Baddireddi Subhadra email: lakshmibs@annauniv.edu organization: Centre for Biotechnology, Anna University, India |
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Keywords | IRTK MTT-3-(4,5-Dimethylthiazol-2-yl)-2,5 IRS Glycogen synthesis DMEM LDH Glucose uptake PI3K RT-PCR 2-DOG GSK3 β 3T3-L1 adipocytes WT 3β-Taraxerol NIDDM NBT PKB Mangifera indica EAE IRβ pNPP GS Gen GSK3β NMR PTP1B BCIP GLUT4 GAPDH |
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SubjectTerms | 3T3-L1 adipocytes 3β-Taraxerol Glucose uptake Glycogen synthesis GSK3β Mangifera indica PI3K |
Title | 3β-taraxerol of Mangifera indica, a PI3K dependent dual activator of glucose transport and glycogen synthesis in 3T3-L1 adipocytes |
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