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Phytochemical Fingerprinting and In Vitro Bioassays of the Ethnomedicinal Fern Tectaria coadunata (J. Smith) C. Christensen from Central Nepal

Tectaria coadunata, an ethnomedicinal fern used in Nepal to treat a large number of diseases, has been poorly studied with regard to its phytochemical composition and possible bioactivity. This study was performed with the aim of supporting traditional medicine as a new source of bioactive constitue...

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Autores principales: Shrestha, Shyam Sharan, Sut, Stefania, Barbon Di Marco, Serena, Zengin, Gokhan, Gandin, Valentina, De Franco, Michele, Pant, Deepak Raj, Mahomoodally, Mohamad Fawzi, Dall’Acqua, Stefano, Rajbhandary, Sangeeta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943667/
https://www.ncbi.nlm.nih.gov/pubmed/31817382
http://dx.doi.org/10.3390/molecules24244457
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author Shrestha, Shyam Sharan
Sut, Stefania
Barbon Di Marco, Serena
Zengin, Gokhan
Gandin, Valentina
De Franco, Michele
Pant, Deepak Raj
Mahomoodally, Mohamad Fawzi
Dall’Acqua, Stefano
Rajbhandary, Sangeeta
author_facet Shrestha, Shyam Sharan
Sut, Stefania
Barbon Di Marco, Serena
Zengin, Gokhan
Gandin, Valentina
De Franco, Michele
Pant, Deepak Raj
Mahomoodally, Mohamad Fawzi
Dall’Acqua, Stefano
Rajbhandary, Sangeeta
author_sort Shrestha, Shyam Sharan
collection PubMed
description Tectaria coadunata, an ethnomedicinal fern used in Nepal to treat a large number of diseases, has been poorly studied with regard to its phytochemical composition and possible bioactivity. This study was performed with the aim of supporting traditional medicine as a new source of bioactive constituents. Phytochemical compositions of methanol extracts were determined by nuclear magnetic resonance (NMR), liquid chromatography–diode array detector–mass spectrophotometry (LC-DAD-MS), and liquid chromatography–fluorescence–mass spectrometry. Quali-quantitative data revealed large amount of procyanidins, mainly of the A-type, as well as eriodictyol-7-O-glucuronide and luteolin-7-O-glucoronide as main constituents. The antioxidant, cytotoxic, and inhibitory activity of five enzymes that are implicated in human diseases was evaluated for the extract and fractions. High free-radical scavenging activity in 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) assays and inhibitory activities against cholinesterases and tyrosinase were observed. Furthermore, a moderate cytotoxic effect was observed on the 2008 and BxPC3 cell lines. Overall results showed potential usefulness of this fern as a source of phytochemicals for pharmaceutical uses.
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spelling pubmed-69436672020-01-10 Phytochemical Fingerprinting and In Vitro Bioassays of the Ethnomedicinal Fern Tectaria coadunata (J. Smith) C. Christensen from Central Nepal Shrestha, Shyam Sharan Sut, Stefania Barbon Di Marco, Serena Zengin, Gokhan Gandin, Valentina De Franco, Michele Pant, Deepak Raj Mahomoodally, Mohamad Fawzi Dall’Acqua, Stefano Rajbhandary, Sangeeta Molecules Article Tectaria coadunata, an ethnomedicinal fern used in Nepal to treat a large number of diseases, has been poorly studied with regard to its phytochemical composition and possible bioactivity. This study was performed with the aim of supporting traditional medicine as a new source of bioactive constituents. Phytochemical compositions of methanol extracts were determined by nuclear magnetic resonance (NMR), liquid chromatography–diode array detector–mass spectrophotometry (LC-DAD-MS), and liquid chromatography–fluorescence–mass spectrometry. Quali-quantitative data revealed large amount of procyanidins, mainly of the A-type, as well as eriodictyol-7-O-glucuronide and luteolin-7-O-glucoronide as main constituents. The antioxidant, cytotoxic, and inhibitory activity of five enzymes that are implicated in human diseases was evaluated for the extract and fractions. High free-radical scavenging activity in 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) assays and inhibitory activities against cholinesterases and tyrosinase were observed. Furthermore, a moderate cytotoxic effect was observed on the 2008 and BxPC3 cell lines. Overall results showed potential usefulness of this fern as a source of phytochemicals for pharmaceutical uses. MDPI 2019-12-05 /pmc/articles/PMC6943667/ /pubmed/31817382 http://dx.doi.org/10.3390/molecules24244457 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shrestha, Shyam Sharan
Sut, Stefania
Barbon Di Marco, Serena
Zengin, Gokhan
Gandin, Valentina
De Franco, Michele
Pant, Deepak Raj
Mahomoodally, Mohamad Fawzi
Dall’Acqua, Stefano
Rajbhandary, Sangeeta
Phytochemical Fingerprinting and In Vitro Bioassays of the Ethnomedicinal Fern Tectaria coadunata (J. Smith) C. Christensen from Central Nepal
title Phytochemical Fingerprinting and In Vitro Bioassays of the Ethnomedicinal Fern Tectaria coadunata (J. Smith) C. Christensen from Central Nepal
title_full Phytochemical Fingerprinting and In Vitro Bioassays of the Ethnomedicinal Fern Tectaria coadunata (J. Smith) C. Christensen from Central Nepal
title_fullStr Phytochemical Fingerprinting and In Vitro Bioassays of the Ethnomedicinal Fern Tectaria coadunata (J. Smith) C. Christensen from Central Nepal
title_full_unstemmed Phytochemical Fingerprinting and In Vitro Bioassays of the Ethnomedicinal Fern Tectaria coadunata (J. Smith) C. Christensen from Central Nepal
title_short Phytochemical Fingerprinting and In Vitro Bioassays of the Ethnomedicinal Fern Tectaria coadunata (J. Smith) C. Christensen from Central Nepal
title_sort phytochemical fingerprinting and in vitro bioassays of the ethnomedicinal fern tectaria coadunata (j. smith) c. christensen from central nepal
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943667/
https://www.ncbi.nlm.nih.gov/pubmed/31817382
http://dx.doi.org/10.3390/molecules24244457
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