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Chemical Profile and Antioxidant Activity of Zinnia elegans Jacq. Fractions

Zinnia elegans (syn. Zinnia violacea) is a common ornamental plant of the Asteraceae family, widely cultivated for the impressive range of flower colors and persistent bloom. Given its uncomplicated cultivation and high adaptability to harsh landscape conditions, we investigated the potential use of...

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Autores principales: Burlec, Ana Flavia, Pecio, Łukasz, Mircea, Cornelia, Cioancă, Oana, Corciovă, Andreia, Nicolescu, Alina, Oleszek, Wiesław, Hăncianu, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720917/
https://www.ncbi.nlm.nih.gov/pubmed/31412649
http://dx.doi.org/10.3390/molecules24162934
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author Burlec, Ana Flavia
Pecio, Łukasz
Mircea, Cornelia
Cioancă, Oana
Corciovă, Andreia
Nicolescu, Alina
Oleszek, Wiesław
Hăncianu, Monica
author_facet Burlec, Ana Flavia
Pecio, Łukasz
Mircea, Cornelia
Cioancă, Oana
Corciovă, Andreia
Nicolescu, Alina
Oleszek, Wiesław
Hăncianu, Monica
author_sort Burlec, Ana Flavia
collection PubMed
description Zinnia elegans (syn. Zinnia violacea) is a common ornamental plant of the Asteraceae family, widely cultivated for the impressive range of flower colors and persistent bloom. Given its uncomplicated cultivation and high adaptability to harsh landscape conditions, we investigated the potential use of Z. elegans as a source of valuable secondary metabolites. Preliminary classification of compounds found in a methanolic extract obtained from inflorescences of Z. elegans cv. Caroussel was accomplished using HR LC-MS techniques. The extract was then subjected to solid-phase extraction and separation using Sephadex LH-20 column chromatography, which resulted in several fractions further investigated for their antioxidant properties through lipoxygenase inhibition and metal chelating activity assays. Moreover, following additional purification procedures, structures of some active ingredients were established by NMR spectroscopy. The investigated fractions contained polyphenolic compounds such as chlorogenic acids and apigenin, kaempferol, and quercetin glycosides. Antioxidant assays showed that certain fractions exhibit moderate 15-LOX inhibition (Fr 2, IC(50) = 18.98 μg/mL) and metal chelation (e.g., Fr 1-2, EC(50) = 0.714–1.037 mg/mL) activities as compared to positive controls (20.25 μg/mL for kaempferol and 0.068 mg/mL for EDTA, respectively). For Fr 2, the 15-LOX inhibition activity seems to be related to the abundance of kaempferol glycosides. The NMR analyses revealed the presence of a kaempferol 3-O-glycoside, and a guanidine alkaloid previously not described in this species.
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spelling pubmed-67209172019-09-10 Chemical Profile and Antioxidant Activity of Zinnia elegans Jacq. Fractions Burlec, Ana Flavia Pecio, Łukasz Mircea, Cornelia Cioancă, Oana Corciovă, Andreia Nicolescu, Alina Oleszek, Wiesław Hăncianu, Monica Molecules Article Zinnia elegans (syn. Zinnia violacea) is a common ornamental plant of the Asteraceae family, widely cultivated for the impressive range of flower colors and persistent bloom. Given its uncomplicated cultivation and high adaptability to harsh landscape conditions, we investigated the potential use of Z. elegans as a source of valuable secondary metabolites. Preliminary classification of compounds found in a methanolic extract obtained from inflorescences of Z. elegans cv. Caroussel was accomplished using HR LC-MS techniques. The extract was then subjected to solid-phase extraction and separation using Sephadex LH-20 column chromatography, which resulted in several fractions further investigated for their antioxidant properties through lipoxygenase inhibition and metal chelating activity assays. Moreover, following additional purification procedures, structures of some active ingredients were established by NMR spectroscopy. The investigated fractions contained polyphenolic compounds such as chlorogenic acids and apigenin, kaempferol, and quercetin glycosides. Antioxidant assays showed that certain fractions exhibit moderate 15-LOX inhibition (Fr 2, IC(50) = 18.98 μg/mL) and metal chelation (e.g., Fr 1-2, EC(50) = 0.714–1.037 mg/mL) activities as compared to positive controls (20.25 μg/mL for kaempferol and 0.068 mg/mL for EDTA, respectively). For Fr 2, the 15-LOX inhibition activity seems to be related to the abundance of kaempferol glycosides. The NMR analyses revealed the presence of a kaempferol 3-O-glycoside, and a guanidine alkaloid previously not described in this species. MDPI 2019-08-13 /pmc/articles/PMC6720917/ /pubmed/31412649 http://dx.doi.org/10.3390/molecules24162934 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
Burlec, Ana Flavia
Pecio, Łukasz
Mircea, Cornelia
Cioancă, Oana
Corciovă, Andreia
Nicolescu, Alina
Oleszek, Wiesław
Hăncianu, Monica
Chemical Profile and Antioxidant Activity of Zinnia elegans Jacq. Fractions
title Chemical Profile and Antioxidant Activity of Zinnia elegans Jacq. Fractions
title_full Chemical Profile and Antioxidant Activity of Zinnia elegans Jacq. Fractions
title_fullStr Chemical Profile and Antioxidant Activity of Zinnia elegans Jacq. Fractions
title_full_unstemmed Chemical Profile and Antioxidant Activity of Zinnia elegans Jacq. Fractions
title_short Chemical Profile and Antioxidant Activity of Zinnia elegans Jacq. Fractions
title_sort chemical profile and antioxidant activity of zinnia elegans jacq. fractions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720917/
https://www.ncbi.nlm.nih.gov/pubmed/31412649
http://dx.doi.org/10.3390/molecules24162934
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