Isoflavonoid Profiling and Estrogen-Like Activity of Four <i>Genista</i> Species from the Greek Flora

As part of our ongoing research on phytoestrogens, we investigated the phytochemical profile and estrogen-like activities of eight extracts from the aerial parts of four <i>Genista</i> species of Greek flora using estrogen-responsive cell lines. Ethyl acetate and methanolic extracts of &...

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Main Authors: Antigoni Cheilari, Argyro Vontzalidou, Maria Makropoulou, Aggeliki K. Meligova, Nikolas Fokialakis, Sofia Mitakou, Michael N. Alexis, Nektarios Aligiannis
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/25/23/5507
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spelling doaj-f2feef92c2a7451fa09452bf39ea75c72020-11-27T07:57:14ZengMDPI AGMolecules1420-30492020-11-01255507550710.3390/molecules25235507Isoflavonoid Profiling and Estrogen-Like Activity of Four <i>Genista</i> Species from the Greek FloraAntigoni Cheilari0Argyro Vontzalidou1Maria Makropoulou2Aggeliki K. Meligova3Nikolas Fokialakis4Sofia Mitakou5Michael N. Alexis6Nektarios Aligiannis7Department of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopoli Zografou, 15771 Athens, GreeceDepartment of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopoli Zografou, 15771 Athens, GreeceDepartment of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopoli Zografou, 15771 Athens, GreeceInstitute of Chemical Biology, National Hellenic Research Foundation, 48, Vassileos Constantinou Avenue, 11635 Athens, GreeceDepartment of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopoli Zografou, 15771 Athens, GreeceDepartment of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopoli Zografou, 15771 Athens, GreeceInstitute of Chemical Biology, National Hellenic Research Foundation, 48, Vassileos Constantinou Avenue, 11635 Athens, GreeceDepartment of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopoli Zografou, 15771 Athens, GreeceAs part of our ongoing research on phytoestrogens, we investigated the phytochemical profile and estrogen-like activities of eight extracts from the aerial parts of four <i>Genista</i> species of Greek flora using estrogen-responsive cell lines. Ethyl acetate and methanolic extracts of <i>G. acanthoclada</i>, <i>G. depressa,</i><i>G. hassertiana,</i> and <i>G. millii</i> were obtained with accelerated solvent extraction and their phytochemical profiles were compared using ultra-high-performance liquid chromatography-high-resolution mass spectrometry (uHPLC-HRMS). Fourteen isoflavonoids, previously isolated from <i>G. halacsyi</i>, were used as reference standards for their identification in the extracts. Thirteen isoflavonoids were detected in both extracts of <i>G. acanthoclada</i> and <i>G. hassertiana</i>, while fewer and far fewer were detected in <i>G. millii</i> and <i>G. depressa,</i> respectively. The ethyl acetate extracts of <i>G. hassertiana</i> and <i>G. acanthoclada</i> displayed 2.45- and 1.79-fold higher, respectively, estrogen-like agonist activity in Ishikawa cells compared to MCF-7 cells at pharmacologically relevant concentrations. Both these extracts, but not that of <i>G. depressa</i>, contained mono- and di-<i>O-</i>β-<span style="font-variant: small-caps;">d</span>-glucosides of genistein as well as the aglycone, all three of which are known to display full estrogen-like activity at lower-than-micromolar concentrations. The possibility of using preparations rich in <i>G. hassertiana</i> and/or <i>G. acanthoclada</i> extracts as a potentially safer substitute for low-dose vaginal estrogen for menopausal symptoms is discussed.https://www.mdpi.com/1420-3049/25/23/5507<i>Genista depressa</i><i>Genista acanthoclada</i><i>Genista millii</i><i>Genista hassertiana</i>isoflavonesestrogen-like activity
collection DOAJ
language English
format Article
sources DOAJ
author Antigoni Cheilari
Argyro Vontzalidou
Maria Makropoulou
Aggeliki K. Meligova
Nikolas Fokialakis
Sofia Mitakou
Michael N. Alexis
Nektarios Aligiannis
spellingShingle Antigoni Cheilari
Argyro Vontzalidou
Maria Makropoulou
Aggeliki K. Meligova
Nikolas Fokialakis
Sofia Mitakou
Michael N. Alexis
Nektarios Aligiannis
Isoflavonoid Profiling and Estrogen-Like Activity of Four <i>Genista</i> Species from the Greek Flora
Molecules
<i>Genista depressa</i>
<i>Genista acanthoclada</i>
<i>Genista millii</i>
<i>Genista hassertiana</i>
isoflavones
estrogen-like activity
author_facet Antigoni Cheilari
Argyro Vontzalidou
Maria Makropoulou
Aggeliki K. Meligova
Nikolas Fokialakis
Sofia Mitakou
Michael N. Alexis
Nektarios Aligiannis
author_sort Antigoni Cheilari
title Isoflavonoid Profiling and Estrogen-Like Activity of Four <i>Genista</i> Species from the Greek Flora
title_short Isoflavonoid Profiling and Estrogen-Like Activity of Four <i>Genista</i> Species from the Greek Flora
title_full Isoflavonoid Profiling and Estrogen-Like Activity of Four <i>Genista</i> Species from the Greek Flora
title_fullStr Isoflavonoid Profiling and Estrogen-Like Activity of Four <i>Genista</i> Species from the Greek Flora
title_full_unstemmed Isoflavonoid Profiling and Estrogen-Like Activity of Four <i>Genista</i> Species from the Greek Flora
title_sort isoflavonoid profiling and estrogen-like activity of four <i>genista</i> species from the greek flora
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2020-11-01
description As part of our ongoing research on phytoestrogens, we investigated the phytochemical profile and estrogen-like activities of eight extracts from the aerial parts of four <i>Genista</i> species of Greek flora using estrogen-responsive cell lines. Ethyl acetate and methanolic extracts of <i>G. acanthoclada</i>, <i>G. depressa,</i><i>G. hassertiana,</i> and <i>G. millii</i> were obtained with accelerated solvent extraction and their phytochemical profiles were compared using ultra-high-performance liquid chromatography-high-resolution mass spectrometry (uHPLC-HRMS). Fourteen isoflavonoids, previously isolated from <i>G. halacsyi</i>, were used as reference standards for their identification in the extracts. Thirteen isoflavonoids were detected in both extracts of <i>G. acanthoclada</i> and <i>G. hassertiana</i>, while fewer and far fewer were detected in <i>G. millii</i> and <i>G. depressa,</i> respectively. The ethyl acetate extracts of <i>G. hassertiana</i> and <i>G. acanthoclada</i> displayed 2.45- and 1.79-fold higher, respectively, estrogen-like agonist activity in Ishikawa cells compared to MCF-7 cells at pharmacologically relevant concentrations. Both these extracts, but not that of <i>G. depressa</i>, contained mono- and di-<i>O-</i>β-<span style="font-variant: small-caps;">d</span>-glucosides of genistein as well as the aglycone, all three of which are known to display full estrogen-like activity at lower-than-micromolar concentrations. The possibility of using preparations rich in <i>G. hassertiana</i> and/or <i>G. acanthoclada</i> extracts as a potentially safer substitute for low-dose vaginal estrogen for menopausal symptoms is discussed.
topic <i>Genista depressa</i>
<i>Genista acanthoclada</i>
<i>Genista millii</i>
<i>Genista hassertiana</i>
isoflavones
estrogen-like activity
url https://www.mdpi.com/1420-3049/25/23/5507
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