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UHPLC-QTOF-MS/MS based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of Butea monosperma

Butea monosperma is one of the extensively used plants in traditional system of medicines for many therapeutic purposes. In this study, the antioxidant activity, α-glucosidase and α-amylase inhibition properties of freeze drying assisted ultrasonicated leaf extracts (hydro-ethanolic) of B. monosperm...

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Autores principales: Farooq, Muhammad Umar, Mumtaz, Muhammad Waseem, Mukhtar, Hamid, Rashid, Umer, Akhtar, Muhammad Tayyab, Raza, Syed Ali, Nadeem, Muhammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044436/
https://www.ncbi.nlm.nih.gov/pubmed/32103043
http://dx.doi.org/10.1038/s41598-020-60076-5
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author Farooq, Muhammad Umar
Mumtaz, Muhammad Waseem
Mukhtar, Hamid
Rashid, Umer
Akhtar, Muhammad Tayyab
Raza, Syed Ali
Nadeem, Muhammad
author_facet Farooq, Muhammad Umar
Mumtaz, Muhammad Waseem
Mukhtar, Hamid
Rashid, Umer
Akhtar, Muhammad Tayyab
Raza, Syed Ali
Nadeem, Muhammad
author_sort Farooq, Muhammad Umar
collection PubMed
description Butea monosperma is one of the extensively used plants in traditional system of medicines for many therapeutic purposes. In this study, the antioxidant activity, α-glucosidase and α-amylase inhibition properties of freeze drying assisted ultrasonicated leaf extracts (hydro-ethanolic) of B. monosperma have been investigated. The findings revealed that 60% ethanolic fraction exhibited high phenolic contents, total flavonoid contents, highest antioxidant activity, and promising α-glucosidase and α-amylase inhibitions. The UHPLC-QTOF-MS/MS analysis indicated the presence of notable metabolites of significant medicinal potential including apigenin, apigenin C-hexoside C-pentoside, apigenin C-hexoside C-hexoside, apigenin-6,8-di-C-pentoside and genistin etc., in B. monosperma leave extract. Docking studies were carried out to determine the possible role of each phytochemical present in leaf extract. Binding affinity data and interaction pattern of all the possible phytochemicals in leaf extract of B. monosperma revealed that they can inhibit α-amylase and α-glucosidase synergistically to prevent hyperglycemia.
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spelling pubmed-70444362020-03-04 UHPLC-QTOF-MS/MS based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of Butea monosperma Farooq, Muhammad Umar Mumtaz, Muhammad Waseem Mukhtar, Hamid Rashid, Umer Akhtar, Muhammad Tayyab Raza, Syed Ali Nadeem, Muhammad Sci Rep Article Butea monosperma is one of the extensively used plants in traditional system of medicines for many therapeutic purposes. In this study, the antioxidant activity, α-glucosidase and α-amylase inhibition properties of freeze drying assisted ultrasonicated leaf extracts (hydro-ethanolic) of B. monosperma have been investigated. The findings revealed that 60% ethanolic fraction exhibited high phenolic contents, total flavonoid contents, highest antioxidant activity, and promising α-glucosidase and α-amylase inhibitions. The UHPLC-QTOF-MS/MS analysis indicated the presence of notable metabolites of significant medicinal potential including apigenin, apigenin C-hexoside C-pentoside, apigenin C-hexoside C-hexoside, apigenin-6,8-di-C-pentoside and genistin etc., in B. monosperma leave extract. Docking studies were carried out to determine the possible role of each phytochemical present in leaf extract. Binding affinity data and interaction pattern of all the possible phytochemicals in leaf extract of B. monosperma revealed that they can inhibit α-amylase and α-glucosidase synergistically to prevent hyperglycemia. Nature Publishing Group UK 2020-02-26 /pmc/articles/PMC7044436/ /pubmed/32103043 http://dx.doi.org/10.1038/s41598-020-60076-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Farooq, Muhammad Umar
Mumtaz, Muhammad Waseem
Mukhtar, Hamid
Rashid, Umer
Akhtar, Muhammad Tayyab
Raza, Syed Ali
Nadeem, Muhammad
UHPLC-QTOF-MS/MS based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of Butea monosperma
title UHPLC-QTOF-MS/MS based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of Butea monosperma
title_full UHPLC-QTOF-MS/MS based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of Butea monosperma
title_fullStr UHPLC-QTOF-MS/MS based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of Butea monosperma
title_full_unstemmed UHPLC-QTOF-MS/MS based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of Butea monosperma
title_short UHPLC-QTOF-MS/MS based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of Butea monosperma
title_sort uhplc-qtof-ms/ms based phytochemical characterization and anti-hyperglycemic prospective of hydro-ethanolic leaf extract of butea monosperma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044436/
https://www.ncbi.nlm.nih.gov/pubmed/32103043
http://dx.doi.org/10.1038/s41598-020-60076-5
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