Cargando…
Effective Control of Postprandial Glucose Level through Inhibition of Intestinal Alpha Glucosidase by Cymbopogon martinii (Roxb.)
Inhibition of intestinal alpha glucosidase plays a major role in preventing rise in postprandial glucose level in diabetics. Cymbopogon martinii (CM) (family Poaceae) is used in traditional Indian medicine in treatment of diabetes mellitus. The alpha glucosidase inhibitory action of the plant is stu...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139892/ https://www.ncbi.nlm.nih.gov/pubmed/21792369 http://dx.doi.org/10.1155/2012/372909 |
_version_ | 1782208501343322112 |
---|---|
author | Ghadyale, Varsha Takalikar, Shrihari Haldavnekar, Vivek Arvindekar, Akalpita |
author_facet | Ghadyale, Varsha Takalikar, Shrihari Haldavnekar, Vivek Arvindekar, Akalpita |
author_sort | Ghadyale, Varsha |
collection | PubMed |
description | Inhibition of intestinal alpha glucosidase plays a major role in preventing rise in postprandial glucose level in diabetics. Cymbopogon martinii (CM) (family Poaceae) is used in traditional Indian medicine in treatment of diabetes mellitus. The alpha glucosidase inhibitory action of the plant is studied. The active component was separated using hot water extraction of the whole plant powder, differential solvent extraction, and silica gel column chromatography. The 30 : 70 toluene : ethyl acetate fraction showed optimum activity. The silica gel chromatography fraction demonstrated 98, 98, and 68% inhibition for starch, maltose, and sucrose, respectively, at 5 mg/kg body weight of rats. Intestinal absorption studies using noneverted intestinal sacs, as well as in vivo studies in streptozotocin-induced diabetic rats using oral glucose tolerance with maltose and sucrose load, revealed better inhibition of alpha glucosidase as compared to acarbose. Kinetic studies using Lineweaver Burk plot showed mixed to noncompetitive type of inhibition by CM. In vivo studies with maltose load of 2 mg and 3 mg/gm body weight showed a noncompetitive pattern of inhibition at 5 mg/kg body weight of CM as against 60 mg/kg body weight of acarbose. Thus CM is more effective alpha glucosidase inhibitor and at lower concentration than acarbose. |
format | Online Article Text |
id | pubmed-3139892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-31398922011-07-26 Effective Control of Postprandial Glucose Level through Inhibition of Intestinal Alpha Glucosidase by Cymbopogon martinii (Roxb.) Ghadyale, Varsha Takalikar, Shrihari Haldavnekar, Vivek Arvindekar, Akalpita Evid Based Complement Alternat Med Research Article Inhibition of intestinal alpha glucosidase plays a major role in preventing rise in postprandial glucose level in diabetics. Cymbopogon martinii (CM) (family Poaceae) is used in traditional Indian medicine in treatment of diabetes mellitus. The alpha glucosidase inhibitory action of the plant is studied. The active component was separated using hot water extraction of the whole plant powder, differential solvent extraction, and silica gel column chromatography. The 30 : 70 toluene : ethyl acetate fraction showed optimum activity. The silica gel chromatography fraction demonstrated 98, 98, and 68% inhibition for starch, maltose, and sucrose, respectively, at 5 mg/kg body weight of rats. Intestinal absorption studies using noneverted intestinal sacs, as well as in vivo studies in streptozotocin-induced diabetic rats using oral glucose tolerance with maltose and sucrose load, revealed better inhibition of alpha glucosidase as compared to acarbose. Kinetic studies using Lineweaver Burk plot showed mixed to noncompetitive type of inhibition by CM. In vivo studies with maltose load of 2 mg and 3 mg/gm body weight showed a noncompetitive pattern of inhibition at 5 mg/kg body weight of CM as against 60 mg/kg body weight of acarbose. Thus CM is more effective alpha glucosidase inhibitor and at lower concentration than acarbose. Hindawi Publishing Corporation 2012 2011-07-07 /pmc/articles/PMC3139892/ /pubmed/21792369 http://dx.doi.org/10.1155/2012/372909 Text en Copyright © 2012 Varsha Ghadyale et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ghadyale, Varsha Takalikar, Shrihari Haldavnekar, Vivek Arvindekar, Akalpita Effective Control of Postprandial Glucose Level through Inhibition of Intestinal Alpha Glucosidase by Cymbopogon martinii (Roxb.) |
title | Effective Control of Postprandial Glucose Level through Inhibition of Intestinal Alpha Glucosidase by Cymbopogon martinii (Roxb.) |
title_full | Effective Control of Postprandial Glucose Level through Inhibition of Intestinal Alpha Glucosidase by Cymbopogon martinii (Roxb.) |
title_fullStr | Effective Control of Postprandial Glucose Level through Inhibition of Intestinal Alpha Glucosidase by Cymbopogon martinii (Roxb.) |
title_full_unstemmed | Effective Control of Postprandial Glucose Level through Inhibition of Intestinal Alpha Glucosidase by Cymbopogon martinii (Roxb.) |
title_short | Effective Control of Postprandial Glucose Level through Inhibition of Intestinal Alpha Glucosidase by Cymbopogon martinii (Roxb.) |
title_sort | effective control of postprandial glucose level through inhibition of intestinal alpha glucosidase by cymbopogon martinii (roxb.) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139892/ https://www.ncbi.nlm.nih.gov/pubmed/21792369 http://dx.doi.org/10.1155/2012/372909 |
work_keys_str_mv | AT ghadyalevarsha effectivecontrolofpostprandialglucoselevelthroughinhibitionofintestinalalphaglucosidasebycymbopogonmartiniiroxb AT takalikarshrihari effectivecontrolofpostprandialglucoselevelthroughinhibitionofintestinalalphaglucosidasebycymbopogonmartiniiroxb AT haldavnekarvivek effectivecontrolofpostprandialglucoselevelthroughinhibitionofintestinalalphaglucosidasebycymbopogonmartiniiroxb AT arvindekarakalpita effectivecontrolofpostprandialglucoselevelthroughinhibitionofintestinalalphaglucosidasebycymbopogonmartiniiroxb |