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New In Vitro Studies on the Bioprofile of Genista tenera Antihyperglycemic Extract
ABSTRACT: The inhibition of α-glucosidase and glucose-6-phosphatase, two enzymes involved in the carbohydrate metabolism, is an important target to control glycaemia on individuals with type 2 diabetes. In this work we report for the first time the inhibition of both enzymes by the antihyperglycemic...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681709/ https://www.ncbi.nlm.nih.gov/pubmed/26493049 http://dx.doi.org/10.1007/s13659-015-0077-z |
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author | Batista, Daniela Falé, Pedro L. Serralheiro, Maria L. Araújo, Maria E. Madeira, Paulo J. A. Borges, Carlos Torgal, Isabel Goulart, Margarida Justino, Jorge Martins, Alice Rauter, Amélia P. |
author_facet | Batista, Daniela Falé, Pedro L. Serralheiro, Maria L. Araújo, Maria E. Madeira, Paulo J. A. Borges, Carlos Torgal, Isabel Goulart, Margarida Justino, Jorge Martins, Alice Rauter, Amélia P. |
author_sort | Batista, Daniela |
collection | PubMed |
description | ABSTRACT: The inhibition of α-glucosidase and glucose-6-phosphatase, two enzymes involved in the carbohydrate metabolism, is an important target to control glycaemia on individuals with type 2 diabetes. In this work we report for the first time the inhibition of both enzymes by the antihyperglycemic n-butanol extract from Genista tenera (Fabaceae). This extract decreased α-glucosidase and glucose-6-phosphatase activities to 0.97 and 80.25 %, respectively, being more effective than acarbose, and phlorizin, the positive controls, which reduced enzymes activities only to 17.39 and 96.06 %. Once inflammation and oxidative stress are related to diabetic impairments, the anti-inflammatory activity of the extract was also evaluated, through its inhibitory activity over COX-1 enzyme (47.5 % inhibition). Moreover, after induction of oxidative stress by UV radiation, the viability of irradiated rat liver hepatoma cells exposed to the extract was significantly higher (67.82 %) than that promoted by ascorbic acid, the positive control (45.05 %). In addition, the stability of the extract under gastrointestinal conditions was evaluated by HPLC–DAD-ESI–MS/MS. Flavonoid diglycosides were identified as the main constituents of the extract, and no alterations in the chemical composition nor in the antioxidant activity were observed after in vitro digestion with artificial gastric and pancreatic juices. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-4681709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-46817092015-12-22 New In Vitro Studies on the Bioprofile of Genista tenera Antihyperglycemic Extract Batista, Daniela Falé, Pedro L. Serralheiro, Maria L. Araújo, Maria E. Madeira, Paulo J. A. Borges, Carlos Torgal, Isabel Goulart, Margarida Justino, Jorge Martins, Alice Rauter, Amélia P. Nat Prod Bioprospect Original Article ABSTRACT: The inhibition of α-glucosidase and glucose-6-phosphatase, two enzymes involved in the carbohydrate metabolism, is an important target to control glycaemia on individuals with type 2 diabetes. In this work we report for the first time the inhibition of both enzymes by the antihyperglycemic n-butanol extract from Genista tenera (Fabaceae). This extract decreased α-glucosidase and glucose-6-phosphatase activities to 0.97 and 80.25 %, respectively, being more effective than acarbose, and phlorizin, the positive controls, which reduced enzymes activities only to 17.39 and 96.06 %. Once inflammation and oxidative stress are related to diabetic impairments, the anti-inflammatory activity of the extract was also evaluated, through its inhibitory activity over COX-1 enzyme (47.5 % inhibition). Moreover, after induction of oxidative stress by UV radiation, the viability of irradiated rat liver hepatoma cells exposed to the extract was significantly higher (67.82 %) than that promoted by ascorbic acid, the positive control (45.05 %). In addition, the stability of the extract under gastrointestinal conditions was evaluated by HPLC–DAD-ESI–MS/MS. Flavonoid diglycosides were identified as the main constituents of the extract, and no alterations in the chemical composition nor in the antioxidant activity were observed after in vitro digestion with artificial gastric and pancreatic juices. GRAPHICAL ABSTRACT: [Image: see text] Springer Berlin Heidelberg 2015-10-22 /pmc/articles/PMC4681709/ /pubmed/26493049 http://dx.doi.org/10.1007/s13659-015-0077-z Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Batista, Daniela Falé, Pedro L. Serralheiro, Maria L. Araújo, Maria E. Madeira, Paulo J. A. Borges, Carlos Torgal, Isabel Goulart, Margarida Justino, Jorge Martins, Alice Rauter, Amélia P. New In Vitro Studies on the Bioprofile of Genista tenera Antihyperglycemic Extract |
title | New In Vitro Studies on the Bioprofile of Genista tenera Antihyperglycemic Extract |
title_full | New In Vitro Studies on the Bioprofile of Genista tenera Antihyperglycemic Extract |
title_fullStr | New In Vitro Studies on the Bioprofile of Genista tenera Antihyperglycemic Extract |
title_full_unstemmed | New In Vitro Studies on the Bioprofile of Genista tenera Antihyperglycemic Extract |
title_short | New In Vitro Studies on the Bioprofile of Genista tenera Antihyperglycemic Extract |
title_sort | new in vitro studies on the bioprofile of genista tenera antihyperglycemic extract |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681709/ https://www.ncbi.nlm.nih.gov/pubmed/26493049 http://dx.doi.org/10.1007/s13659-015-0077-z |
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