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The Effect of Silymarin Flavonolignans and Their Sulfated Conjugates on Platelet Aggregation and Blood Vessels Ex Vivo

Silymarin is a traditional drug and food supplement employed for numerous liver disorders. The available studies indicate that its activities may be broader, in particular due to claimed benefits in some cardiovascular diseases, but the contributions of individual silymarin components are unclear. T...

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Autores principales: Pourová, Jana, Applová, Lenka, Macáková, Kateřina, Vopršalová, Marie, Migkos, Thomas, Bentanachs, Roger, Biedermann, David, Petrásková, Lucie, Tvrdý, Václav, Hrubša, Marcel, Karlíčková, Jana, Křen, Vladimír, Valentová, Kateřina, Mladěnka, Přemysl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836034/
https://www.ncbi.nlm.nih.gov/pubmed/31554252
http://dx.doi.org/10.3390/nu11102286
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author Pourová, Jana
Applová, Lenka
Macáková, Kateřina
Vopršalová, Marie
Migkos, Thomas
Bentanachs, Roger
Biedermann, David
Petrásková, Lucie
Tvrdý, Václav
Hrubša, Marcel
Karlíčková, Jana
Křen, Vladimír
Valentová, Kateřina
Mladěnka, Přemysl
author_facet Pourová, Jana
Applová, Lenka
Macáková, Kateřina
Vopršalová, Marie
Migkos, Thomas
Bentanachs, Roger
Biedermann, David
Petrásková, Lucie
Tvrdý, Václav
Hrubša, Marcel
Karlíčková, Jana
Křen, Vladimír
Valentová, Kateřina
Mladěnka, Přemysl
author_sort Pourová, Jana
collection PubMed
description Silymarin is a traditional drug and food supplement employed for numerous liver disorders. The available studies indicate that its activities may be broader, in particular due to claimed benefits in some cardiovascular diseases, but the contributions of individual silymarin components are unclear. Therefore, we tested silymarin flavonolignans as pure diastereomers as well as their sulfated metabolites for potential vasorelaxant and antiplatelet effects in isolated rat aorta and in human blood, respectively. Eleven compounds from a panel of 17 tested exhibited a vasorelaxant effect, with half maximal effective concentrations (EC(50)) ranging from 20 to 100 µM, and some substances retained certain activity even in the range of hundreds of nM. Stereomers A were generally more potent as vasorelaxants than stereomers B. Interestingly, the most active compound was a metabolite—silychristin-19-O-sulfate. Although initial experiments showed that silybin, 2,3-dehydrosilybin, and 2,3-dehydrosilychristin were able to substantially block platelet aggregation, their effects were rapidly abolished with decreasing concentration, and were negligible at concentrations ≤100 µM. In conclusion, metabolites of silymarin flavonolignans seem to have biologically relevant vasodilatory properties, but the effect of silymarin components on platelets is low or negligible.
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spelling pubmed-68360342019-11-25 The Effect of Silymarin Flavonolignans and Their Sulfated Conjugates on Platelet Aggregation and Blood Vessels Ex Vivo Pourová, Jana Applová, Lenka Macáková, Kateřina Vopršalová, Marie Migkos, Thomas Bentanachs, Roger Biedermann, David Petrásková, Lucie Tvrdý, Václav Hrubša, Marcel Karlíčková, Jana Křen, Vladimír Valentová, Kateřina Mladěnka, Přemysl Nutrients Article Silymarin is a traditional drug and food supplement employed for numerous liver disorders. The available studies indicate that its activities may be broader, in particular due to claimed benefits in some cardiovascular diseases, but the contributions of individual silymarin components are unclear. Therefore, we tested silymarin flavonolignans as pure diastereomers as well as their sulfated metabolites for potential vasorelaxant and antiplatelet effects in isolated rat aorta and in human blood, respectively. Eleven compounds from a panel of 17 tested exhibited a vasorelaxant effect, with half maximal effective concentrations (EC(50)) ranging from 20 to 100 µM, and some substances retained certain activity even in the range of hundreds of nM. Stereomers A were generally more potent as vasorelaxants than stereomers B. Interestingly, the most active compound was a metabolite—silychristin-19-O-sulfate. Although initial experiments showed that silybin, 2,3-dehydrosilybin, and 2,3-dehydrosilychristin were able to substantially block platelet aggregation, their effects were rapidly abolished with decreasing concentration, and were negligible at concentrations ≤100 µM. In conclusion, metabolites of silymarin flavonolignans seem to have biologically relevant vasodilatory properties, but the effect of silymarin components on platelets is low or negligible. MDPI 2019-09-24 /pmc/articles/PMC6836034/ /pubmed/31554252 http://dx.doi.org/10.3390/nu11102286 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
Pourová, Jana
Applová, Lenka
Macáková, Kateřina
Vopršalová, Marie
Migkos, Thomas
Bentanachs, Roger
Biedermann, David
Petrásková, Lucie
Tvrdý, Václav
Hrubša, Marcel
Karlíčková, Jana
Křen, Vladimír
Valentová, Kateřina
Mladěnka, Přemysl
The Effect of Silymarin Flavonolignans and Their Sulfated Conjugates on Platelet Aggregation and Blood Vessels Ex Vivo
title The Effect of Silymarin Flavonolignans and Their Sulfated Conjugates on Platelet Aggregation and Blood Vessels Ex Vivo
title_full The Effect of Silymarin Flavonolignans and Their Sulfated Conjugates on Platelet Aggregation and Blood Vessels Ex Vivo
title_fullStr The Effect of Silymarin Flavonolignans and Their Sulfated Conjugates on Platelet Aggregation and Blood Vessels Ex Vivo
title_full_unstemmed The Effect of Silymarin Flavonolignans and Their Sulfated Conjugates on Platelet Aggregation and Blood Vessels Ex Vivo
title_short The Effect of Silymarin Flavonolignans and Their Sulfated Conjugates on Platelet Aggregation and Blood Vessels Ex Vivo
title_sort effect of silymarin flavonolignans and their sulfated conjugates on platelet aggregation and blood vessels ex vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836034/
https://www.ncbi.nlm.nih.gov/pubmed/31554252
http://dx.doi.org/10.3390/nu11102286
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