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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
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]
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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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