Modulation of Adhesion Process, E-Selectin and VEGF Production by Anthocyanins and Their Metabolites in an <i>in vitro</i> Model of Atherosclerosis

<b> </b>The present study aims to evaluate the ability of peonidin and petunidin-3-glucoside (Peo-3-glc and Pet-3-glc) and their metabolites (vanillic acid; VA and methyl-gallic acid; MetGA), to prevent monocyte (THP-1) adhesion to endothelial cells (HUVECs), and to reduce the production...

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Main Authors: Mirko Marino, Cristian Del Bo’, Massimiliano Tucci, Dorothy Klimis-Zacas, Patrizia Riso, Marisa Porrini
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/12/3/655
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spelling doaj-4772ab2c693e49e08c9d2b98781001622020-11-25T02:15:06ZengMDPI AGNutrients2072-66432020-02-0112365510.3390/nu12030655nu12030655Modulation of Adhesion Process, E-Selectin and VEGF Production by Anthocyanins and Their Metabolites in an <i>in vitro</i> Model of AtherosclerosisMirko Marino0Cristian Del Bo’1Massimiliano Tucci2Dorothy Klimis-Zacas3Patrizia Riso4Marisa Porrini5Università degli Studi di Milano, Department of Food, Environmental and Nutritional Sciences, Division of Human Nutrition, 20133 Milan, ItalyUniversità degli Studi di Milano, Department of Food, Environmental and Nutritional Sciences, Division of Human Nutrition, 20133 Milan, ItalyUniversità degli Studi di Milano, Department of Food, Environmental and Nutritional Sciences, Division of Human Nutrition, 20133 Milan, ItalySchool of Food and Agriculture, University of Maine, Orono, ME 04469, USAUniversità degli Studi di Milano, Department of Food, Environmental and Nutritional Sciences, Division of Human Nutrition, 20133 Milan, ItalyUniversità degli Studi di Milano, Department of Food, Environmental and Nutritional Sciences, Division of Human Nutrition, 20133 Milan, Italy<b> </b>The present study aims to evaluate the ability of peonidin and petunidin-3-glucoside (Peo-3-glc and Pet-3-glc) and their metabolites (vanillic acid; VA and methyl-gallic acid; MetGA), to prevent monocyte (THP-1) adhesion to endothelial cells (HUVECs), and to reduce the production of vascular cell adhesion molecule (VCAM)-1, E-selectin and vascular endothelial growth factor (VEGF) in a stimulated pro-inflammatory environment, a pivotal step of atherogenesis. Tumor necrosis factor-&#945; (TNF-&#945;; 100 ng mL<sup>&#8722;1</sup>) was used to stimulate the adhesion of labelled monocytes (THP-1) to endothelial cells (HUVECs). Successively, different concentrations of Peo-3-glc and Pet-3-glc (0.02 &#181;M, 0.2 &#181;M, 2 &#181;M and 20 &#181;M), VA and MetGA (0.05 &#181;M, 0.5 &#181;M, 5 &#181;M and 50 &#181;M) were tested. After 24 h, VCAM-1, E-selectin and VEGF were quantified by ELISA, while the adhesion process was measured spectrophotometrically. Peo-3-glc and Pet-3-glc (from 0.02 &#181;M to 20 &#181;M) significantly (<i>p</i> &lt; 0.0001) decreased THP-1 adhesion to HUVECs at all concentrations (&#8722;37%, &#8722;24%, &#8722;30% and &#8722;47% for Peo-3-glc; &#8722;37%, &#8722;33%, &#8722;33% and &#8722;45% for Pet-3-glc). VA, but not MetGA, reduced the adhesion process at 50 &#181;M (&#8722;21%; <i>p</i> &lt; 0.001). At the same concentrations, a significant (<i>p</i> &lt; 0.0001) reduction of E-selectin, but not VCAM-1, was documented. In addition, anthocyanins and their metabolites significantly decreased (<i>p</i><i> </i>&lt; 0.001) VEGF production. The present findings suggest that while Peo-3-glc and Pet-3-glc (but not their metabolites) reduced monocyte adhesion to endothelial cells through suppression of E-selectin production, VEGF production was reduced by both anthocyanins and their metabolites, suggesting a role in the regulation of angiogenesis.https://www.mdpi.com/2072-6643/12/3/655anthocyanins and metabolitesinflammationadhesion moleculesvascular endothelial growth factormonocytesendothelial cells
collection DOAJ
language English
format Article
sources DOAJ
author Mirko Marino
Cristian Del Bo’
Massimiliano Tucci
Dorothy Klimis-Zacas
Patrizia Riso
Marisa Porrini
spellingShingle Mirko Marino
Cristian Del Bo’
Massimiliano Tucci
Dorothy Klimis-Zacas
Patrizia Riso
Marisa Porrini
Modulation of Adhesion Process, E-Selectin and VEGF Production by Anthocyanins and Their Metabolites in an <i>in vitro</i> Model of Atherosclerosis
Nutrients
anthocyanins and metabolites
inflammation
adhesion molecules
vascular endothelial growth factor
monocytes
endothelial cells
author_facet Mirko Marino
Cristian Del Bo’
Massimiliano Tucci
Dorothy Klimis-Zacas
Patrizia Riso
Marisa Porrini
author_sort Mirko Marino
title Modulation of Adhesion Process, E-Selectin and VEGF Production by Anthocyanins and Their Metabolites in an <i>in vitro</i> Model of Atherosclerosis
title_short Modulation of Adhesion Process, E-Selectin and VEGF Production by Anthocyanins and Their Metabolites in an <i>in vitro</i> Model of Atherosclerosis
title_full Modulation of Adhesion Process, E-Selectin and VEGF Production by Anthocyanins and Their Metabolites in an <i>in vitro</i> Model of Atherosclerosis
title_fullStr Modulation of Adhesion Process, E-Selectin and VEGF Production by Anthocyanins and Their Metabolites in an <i>in vitro</i> Model of Atherosclerosis
title_full_unstemmed Modulation of Adhesion Process, E-Selectin and VEGF Production by Anthocyanins and Their Metabolites in an <i>in vitro</i> Model of Atherosclerosis
title_sort modulation of adhesion process, e-selectin and vegf production by anthocyanins and their metabolites in an <i>in vitro</i> model of atherosclerosis
publisher MDPI AG
series Nutrients
issn 2072-6643
publishDate 2020-02-01
description <b> </b>The present study aims to evaluate the ability of peonidin and petunidin-3-glucoside (Peo-3-glc and Pet-3-glc) and their metabolites (vanillic acid; VA and methyl-gallic acid; MetGA), to prevent monocyte (THP-1) adhesion to endothelial cells (HUVECs), and to reduce the production of vascular cell adhesion molecule (VCAM)-1, E-selectin and vascular endothelial growth factor (VEGF) in a stimulated pro-inflammatory environment, a pivotal step of atherogenesis. Tumor necrosis factor-&#945; (TNF-&#945;; 100 ng mL<sup>&#8722;1</sup>) was used to stimulate the adhesion of labelled monocytes (THP-1) to endothelial cells (HUVECs). Successively, different concentrations of Peo-3-glc and Pet-3-glc (0.02 &#181;M, 0.2 &#181;M, 2 &#181;M and 20 &#181;M), VA and MetGA (0.05 &#181;M, 0.5 &#181;M, 5 &#181;M and 50 &#181;M) were tested. After 24 h, VCAM-1, E-selectin and VEGF were quantified by ELISA, while the adhesion process was measured spectrophotometrically. Peo-3-glc and Pet-3-glc (from 0.02 &#181;M to 20 &#181;M) significantly (<i>p</i> &lt; 0.0001) decreased THP-1 adhesion to HUVECs at all concentrations (&#8722;37%, &#8722;24%, &#8722;30% and &#8722;47% for Peo-3-glc; &#8722;37%, &#8722;33%, &#8722;33% and &#8722;45% for Pet-3-glc). VA, but not MetGA, reduced the adhesion process at 50 &#181;M (&#8722;21%; <i>p</i> &lt; 0.001). At the same concentrations, a significant (<i>p</i> &lt; 0.0001) reduction of E-selectin, but not VCAM-1, was documented. In addition, anthocyanins and their metabolites significantly decreased (<i>p</i><i> </i>&lt; 0.001) VEGF production. The present findings suggest that while Peo-3-glc and Pet-3-glc (but not their metabolites) reduced monocyte adhesion to endothelial cells through suppression of E-selectin production, VEGF production was reduced by both anthocyanins and their metabolites, suggesting a role in the regulation of angiogenesis.
topic anthocyanins and metabolites
inflammation
adhesion molecules
vascular endothelial growth factor
monocytes
endothelial cells
url https://www.mdpi.com/2072-6643/12/3/655
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