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Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea
Many medicinal plants around the world are used for therapeutic purposes against several diseases, including diabetes mellitus. Due to their composition of natural substances that are effective and do not represent side effects for users, unlike synthetic drugs, in this study, we investigated the in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136516/ https://www.ncbi.nlm.nih.gov/pubmed/30228829 http://dx.doi.org/10.1155/2018/9589472 |
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author | Ouassou, Hayat Zahidi, Touda Bouknana, Saliha Bouhrim, Mohamed Mekhfi, Hassane Ziyyat, Abderrahim Legssyer, abdekhaleq Aziz, Mohamed Bnouham, Mohamed |
author_facet | Ouassou, Hayat Zahidi, Touda Bouknana, Saliha Bouhrim, Mohamed Mekhfi, Hassane Ziyyat, Abderrahim Legssyer, abdekhaleq Aziz, Mohamed Bnouham, Mohamed |
author_sort | Ouassou, Hayat |
collection | PubMed |
description | Many medicinal plants around the world are used for therapeutic purposes against several diseases, including diabetes mellitus. Due to their composition of natural substances that are effective and do not represent side effects for users, unlike synthetic drugs, in this study, we investigated the inhibitory effect of Caralluma europaea (CE) on α-glucosidase activity in vitro; then the kinetics of the enzyme were studied with increasing concentrations of sucrose in order to determine the inhibition type of the enzyme. In addition, this effect of Caralluma europaea (CE) was confirmed in vivo using rats as an experimental animal model. Among the five fractions of CE, only the ethyl acetate fraction of C. europaea (EACe) induced a significant inhibition of α-glucosidase and its inhibition mode was competitive. The in vivo studies were conducted on mice and rats using glucose and sucrose as a substrate, respectively, to determine the oral glucose tolerance test (OGTT). The results obtained showed that the EACe and the aqueous extract of C. europaea (AECe) have significantly reduced the postprandial hyperglycemia after sucrose and glucose loading in normal and diabetic rats. AECe, also, significantly decreased intestinal glucose absorption, in situ. The results obtained showed that Caralluma europaea has a significant antihyperglycemic activity, which could be due to the inhibition of α-glucosidase activity and enteric absorption of glucose. |
format | Online Article Text |
id | pubmed-6136516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-61365162018-09-18 Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea Ouassou, Hayat Zahidi, Touda Bouknana, Saliha Bouhrim, Mohamed Mekhfi, Hassane Ziyyat, Abderrahim Legssyer, abdekhaleq Aziz, Mohamed Bnouham, Mohamed Evid Based Complement Alternat Med Research Article Many medicinal plants around the world are used for therapeutic purposes against several diseases, including diabetes mellitus. Due to their composition of natural substances that are effective and do not represent side effects for users, unlike synthetic drugs, in this study, we investigated the inhibitory effect of Caralluma europaea (CE) on α-glucosidase activity in vitro; then the kinetics of the enzyme were studied with increasing concentrations of sucrose in order to determine the inhibition type of the enzyme. In addition, this effect of Caralluma europaea (CE) was confirmed in vivo using rats as an experimental animal model. Among the five fractions of CE, only the ethyl acetate fraction of C. europaea (EACe) induced a significant inhibition of α-glucosidase and its inhibition mode was competitive. The in vivo studies were conducted on mice and rats using glucose and sucrose as a substrate, respectively, to determine the oral glucose tolerance test (OGTT). The results obtained showed that the EACe and the aqueous extract of C. europaea (AECe) have significantly reduced the postprandial hyperglycemia after sucrose and glucose loading in normal and diabetic rats. AECe, also, significantly decreased intestinal glucose absorption, in situ. The results obtained showed that Caralluma europaea has a significant antihyperglycemic activity, which could be due to the inhibition of α-glucosidase activity and enteric absorption of glucose. Hindawi 2018-08-29 /pmc/articles/PMC6136516/ /pubmed/30228829 http://dx.doi.org/10.1155/2018/9589472 Text en Copyright © 2018 Hayat Ouassou et al. https://creativecommons.org/licenses/by/4.0/ 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 Ouassou, Hayat Zahidi, Touda Bouknana, Saliha Bouhrim, Mohamed Mekhfi, Hassane Ziyyat, Abderrahim Legssyer, abdekhaleq Aziz, Mohamed Bnouham, Mohamed Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea |
title | Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea |
title_full | Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea |
title_fullStr | Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea |
title_full_unstemmed | Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea |
title_short | Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea |
title_sort | inhibition of α-glucosidase, intestinal glucose absorption, and antidiabetic properties by caralluma europaea |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136516/ https://www.ncbi.nlm.nih.gov/pubmed/30228829 http://dx.doi.org/10.1155/2018/9589472 |
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