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Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo

The major goal in the treatment of diabetes mellitus is to achieve near-normal glycemic control. To optimize both fasting blood glucose and postprandial glucose levels is important in keeping blood glucose levels as close to normal as possible. α-Glucosidase is the enzyme that digests dietary carboh...

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Autores principales: Lee, Soo-Kyung, Hwang, Ji-Yeon, Song, Ji-Hyun, Jo, Ja-Rim, Kim, Myung-Jin, Kim, Mi-Eun, Kim, Jung-In
Formato: Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2849020/
https://www.ncbi.nlm.nih.gov/pubmed/20368936
http://dx.doi.org/10.4162/nrp.2007.1.3.184
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author Lee, Soo-Kyung
Hwang, Ji-Yeon
Song, Ji-Hyun
Jo, Ja-Rim
Kim, Myung-Jin
Kim, Mi-Eun
Kim, Jung-In
author_facet Lee, Soo-Kyung
Hwang, Ji-Yeon
Song, Ji-Hyun
Jo, Ja-Rim
Kim, Myung-Jin
Kim, Mi-Eun
Kim, Jung-In
author_sort Lee, Soo-Kyung
collection PubMed
description The major goal in the treatment of diabetes mellitus is to achieve near-normal glycemic control. To optimize both fasting blood glucose and postprandial glucose levels is important in keeping blood glucose levels as close to normal as possible. α-Glucosidase is the enzyme that digests dietary carbohydrate, and inhibition of this enzyme could suppress postprandial hyperglycemia. The purpose of this study was to test the inhibitory activity of methanol extract of Euonymus alatus on α-glucosidase in vitro and in vivo to evaluate its possible use as an anti-diabetic agent. Yeast α-glucosidase inhibitory activities of methanol extract of E. alatus were measured at concentrations of 0.50, 0.25, 0.10, and 0.05 mg/ml. The ability of E. alatus to lower postprandial glucose was studied in streptozotocin-induced diabetic rats. A starch solution (1 g/kg) with and without E. alatus extract (500 mg/kg) was administered to diabetic rats by gastric intubation after an overnight fast. Plasma glucose levels were measured at 30, 60, 90, 120, 180, and 240 min. Plasma glucose levels were expressed in increments from baseline, and incremental areas under the response curve were calculated. Extract of E. alatus,which had an IC(50) value of 0.272 mg/ml, inhibited yeast α-glucosidase activity in a concentration-dependent manner. A single oral dose of E. alatus extract significantly inhibited increases in blood glucose levels at 60 and 90 min (p<0.05) and significantly decreased incremental response areas under the glycemic response curve (p<0.05). These results suggest that E. alatus has an antihyperglycemic effect by inhibiting α-glucosidase activity in this animal model of diabetes mellitus.
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spelling pubmed-28490202010-04-05 Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo Lee, Soo-Kyung Hwang, Ji-Yeon Song, Ji-Hyun Jo, Ja-Rim Kim, Myung-Jin Kim, Mi-Eun Kim, Jung-In Nutr Res Pract Original Research The major goal in the treatment of diabetes mellitus is to achieve near-normal glycemic control. To optimize both fasting blood glucose and postprandial glucose levels is important in keeping blood glucose levels as close to normal as possible. α-Glucosidase is the enzyme that digests dietary carbohydrate, and inhibition of this enzyme could suppress postprandial hyperglycemia. The purpose of this study was to test the inhibitory activity of methanol extract of Euonymus alatus on α-glucosidase in vitro and in vivo to evaluate its possible use as an anti-diabetic agent. Yeast α-glucosidase inhibitory activities of methanol extract of E. alatus were measured at concentrations of 0.50, 0.25, 0.10, and 0.05 mg/ml. The ability of E. alatus to lower postprandial glucose was studied in streptozotocin-induced diabetic rats. A starch solution (1 g/kg) with and without E. alatus extract (500 mg/kg) was administered to diabetic rats by gastric intubation after an overnight fast. Plasma glucose levels were measured at 30, 60, 90, 120, 180, and 240 min. Plasma glucose levels were expressed in increments from baseline, and incremental areas under the response curve were calculated. Extract of E. alatus,which had an IC(50) value of 0.272 mg/ml, inhibited yeast α-glucosidase activity in a concentration-dependent manner. A single oral dose of E. alatus extract significantly inhibited increases in blood glucose levels at 60 and 90 min (p<0.05) and significantly decreased incremental response areas under the glycemic response curve (p<0.05). These results suggest that E. alatus has an antihyperglycemic effect by inhibiting α-glucosidase activity in this animal model of diabetes mellitus. The Korean Nutrition Society and the Korean Society of Community Nutrition 2007 2007-09-30 /pmc/articles/PMC2849020/ /pubmed/20368936 http://dx.doi.org/10.4162/nrp.2007.1.3.184 Text en ©2007 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Lee, Soo-Kyung
Hwang, Ji-Yeon
Song, Ji-Hyun
Jo, Ja-Rim
Kim, Myung-Jin
Kim, Mi-Eun
Kim, Jung-In
Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo
title Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo
title_full Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo
title_fullStr Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo
title_full_unstemmed Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo
title_short Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo
title_sort inhibitory activity of euonymus alatus against alpha-glucosidase in vitro and in vivo
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2849020/
https://www.ncbi.nlm.nih.gov/pubmed/20368936
http://dx.doi.org/10.4162/nrp.2007.1.3.184
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