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Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism

BACKGROUND: In the present study, we tested a 50% ethanolic extract of Orthosiphon stamineus plants and its isolated bioactive compound with respect to their α-glucosidase and α-amylase inhibitory activities. METHODS: Bioactive flavonoid sinensetin was isolated from 50% ethanolic extract of Orthosip...

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Autores principales: Mohamed, Elsnoussi Ali Hussin, Siddiqui, Mohammad Jamshed Ahmad, Ang, Lee Fung, Sadikun, Amirin, Chan, Sue Hay, Tan, Soo Choon, Asmawi, Mohd Zaini, Yam, Mun Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533584/
https://www.ncbi.nlm.nih.gov/pubmed/23039079
http://dx.doi.org/10.1186/1472-6882-12-176
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author Mohamed, Elsnoussi Ali Hussin
Siddiqui, Mohammad Jamshed Ahmad
Ang, Lee Fung
Sadikun, Amirin
Chan, Sue Hay
Tan, Soo Choon
Asmawi, Mohd Zaini
Yam, Mun Fei
author_facet Mohamed, Elsnoussi Ali Hussin
Siddiqui, Mohammad Jamshed Ahmad
Ang, Lee Fung
Sadikun, Amirin
Chan, Sue Hay
Tan, Soo Choon
Asmawi, Mohd Zaini
Yam, Mun Fei
author_sort Mohamed, Elsnoussi Ali Hussin
collection PubMed
description BACKGROUND: In the present study, we tested a 50% ethanolic extract of Orthosiphon stamineus plants and its isolated bioactive compound with respect to their α-glucosidase and α-amylase inhibitory activities. METHODS: Bioactive flavonoid sinensetin was isolated from 50% ethanolic extract of Orthosiphon stamineus. The structure of this pure compound was determined on the NMR data and the α-glucosidase and α-amylase inhibitory activities of isolated sinensetin and 50% ethanolic extract of Orthosiphon stamineus were evaluated. RESULTS: In vitro studies of a 50% ethanolic extract of O. stamineus and the isolated sinensetin compound showed inhibitory activity on α-glucosidase (IC(50): 4.63 and 0.66 mg/ml, respectively) and α-amylase (IC(50): 36.70 mg/ml and 1.13 mg/ml, respectively). Inhibition of these enzymes provides a strong biochemical basis for the management of type 2 diabetes via the control of glucose absorption. CONCLUSION: Alpha-glucosidase and α-amylase inhibition could the mechanisms through which the 50% ethanolic extract of O. stamineus and sinensetin exert their antidiabetic activity, indicating that it could have potential use in the management of non-insulin-dependent diabetes.
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spelling pubmed-35335842013-01-03 Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism Mohamed, Elsnoussi Ali Hussin Siddiqui, Mohammad Jamshed Ahmad Ang, Lee Fung Sadikun, Amirin Chan, Sue Hay Tan, Soo Choon Asmawi, Mohd Zaini Yam, Mun Fei BMC Complement Altern Med Research Article BACKGROUND: In the present study, we tested a 50% ethanolic extract of Orthosiphon stamineus plants and its isolated bioactive compound with respect to their α-glucosidase and α-amylase inhibitory activities. METHODS: Bioactive flavonoid sinensetin was isolated from 50% ethanolic extract of Orthosiphon stamineus. The structure of this pure compound was determined on the NMR data and the α-glucosidase and α-amylase inhibitory activities of isolated sinensetin and 50% ethanolic extract of Orthosiphon stamineus were evaluated. RESULTS: In vitro studies of a 50% ethanolic extract of O. stamineus and the isolated sinensetin compound showed inhibitory activity on α-glucosidase (IC(50): 4.63 and 0.66 mg/ml, respectively) and α-amylase (IC(50): 36.70 mg/ml and 1.13 mg/ml, respectively). Inhibition of these enzymes provides a strong biochemical basis for the management of type 2 diabetes via the control of glucose absorption. CONCLUSION: Alpha-glucosidase and α-amylase inhibition could the mechanisms through which the 50% ethanolic extract of O. stamineus and sinensetin exert their antidiabetic activity, indicating that it could have potential use in the management of non-insulin-dependent diabetes. BioMed Central 2012-10-08 /pmc/articles/PMC3533584/ /pubmed/23039079 http://dx.doi.org/10.1186/1472-6882-12-176 Text en Copyright ©2012 Mohamed et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mohamed, Elsnoussi Ali Hussin
Siddiqui, Mohammad Jamshed Ahmad
Ang, Lee Fung
Sadikun, Amirin
Chan, Sue Hay
Tan, Soo Choon
Asmawi, Mohd Zaini
Yam, Mun Fei
Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism
title Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism
title_full Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism
title_fullStr Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism
title_full_unstemmed Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism
title_short Potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism
title_sort potent α-glucosidase and α-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from orthosiphon stamineus benth as anti-diabetic mechanism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533584/
https://www.ncbi.nlm.nih.gov/pubmed/23039079
http://dx.doi.org/10.1186/1472-6882-12-176
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