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Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial Vesiculation

SCOPE: Diet rich in bilberries is considered cardioprotective, but the mechanisms of action are poorly understood. Cardiovascular disease is characterized by increased proatherogenic status and high levels of circulating microvesicles (MVs). In an open‐label study patients with myocardial infarction...

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Autores principales: Bryl‐Górecka, Paulina, Sathanoori, Ramasri, Arevström, Lilith, Landberg, Rikard, Bergh, Cecilia, Evander, Mikael, Olde, Björn, Laurell, Thomas, Fröbert, Ole, Erlinge, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685140/
https://www.ncbi.nlm.nih.gov/pubmed/32846041
http://dx.doi.org/10.1002/mnfr.202000108
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author Bryl‐Górecka, Paulina
Sathanoori, Ramasri
Arevström, Lilith
Landberg, Rikard
Bergh, Cecilia
Evander, Mikael
Olde, Björn
Laurell, Thomas
Fröbert, Ole
Erlinge, David
author_facet Bryl‐Górecka, Paulina
Sathanoori, Ramasri
Arevström, Lilith
Landberg, Rikard
Bergh, Cecilia
Evander, Mikael
Olde, Björn
Laurell, Thomas
Fröbert, Ole
Erlinge, David
author_sort Bryl‐Górecka, Paulina
collection PubMed
description SCOPE: Diet rich in bilberries is considered cardioprotective, but the mechanisms of action are poorly understood. Cardiovascular disease is characterized by increased proatherogenic status and high levels of circulating microvesicles (MVs). In an open‐label study patients with myocardial infarction receive an 8 week dietary supplementation with bilberry extract (BE). The effect of BE on patient MV levels and its influence on endothelial vesiculation in vitro is investigated. METHODS AND RESULTS: MVs are captured with acoustic trapping and platelet‐derived MVs (PMVs), as well as endothelial‐derived MVs (EMVs) are quantified with flow cytometry. The in vitro effect of BE on endothelial extracellular vesicle (EV) release is examined using endothelial cells and calcein staining. The mechanisms of BE influence on vesiculation pathways are studied by Western blot and qRT‐PCR. Supplementation with BE decreased both PMVs and EMVs. Furthermore, BE reduced endothelial EV release, Akt phosphorylation, and vesiculation‐related gene transcription. It also protects the cells from P2X(7)‐induced EV release and increase in vesiculation‐related gene expression. CONCLUSION: BE supplementation improves the MV profile in patient blood and reduces endothelial vesiculation through several molecular mechanisms related to the P2X(7) receptor. The findings provide new insight into the cardioprotective effects of bilberries.
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spelling pubmed-76851402020-12-03 Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial Vesiculation Bryl‐Górecka, Paulina Sathanoori, Ramasri Arevström, Lilith Landberg, Rikard Bergh, Cecilia Evander, Mikael Olde, Björn Laurell, Thomas Fröbert, Ole Erlinge, David Mol Nutr Food Res Research Articles SCOPE: Diet rich in bilberries is considered cardioprotective, but the mechanisms of action are poorly understood. Cardiovascular disease is characterized by increased proatherogenic status and high levels of circulating microvesicles (MVs). In an open‐label study patients with myocardial infarction receive an 8 week dietary supplementation with bilberry extract (BE). The effect of BE on patient MV levels and its influence on endothelial vesiculation in vitro is investigated. METHODS AND RESULTS: MVs are captured with acoustic trapping and platelet‐derived MVs (PMVs), as well as endothelial‐derived MVs (EMVs) are quantified with flow cytometry. The in vitro effect of BE on endothelial extracellular vesicle (EV) release is examined using endothelial cells and calcein staining. The mechanisms of BE influence on vesiculation pathways are studied by Western blot and qRT‐PCR. Supplementation with BE decreased both PMVs and EMVs. Furthermore, BE reduced endothelial EV release, Akt phosphorylation, and vesiculation‐related gene transcription. It also protects the cells from P2X(7)‐induced EV release and increase in vesiculation‐related gene expression. CONCLUSION: BE supplementation improves the MV profile in patient blood and reduces endothelial vesiculation through several molecular mechanisms related to the P2X(7) receptor. The findings provide new insight into the cardioprotective effects of bilberries. John Wiley and Sons Inc. 2020-09-10 2020-10 /pmc/articles/PMC7685140/ /pubmed/32846041 http://dx.doi.org/10.1002/mnfr.202000108 Text en © 2020 The Authors. Published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Bryl‐Górecka, Paulina
Sathanoori, Ramasri
Arevström, Lilith
Landberg, Rikard
Bergh, Cecilia
Evander, Mikael
Olde, Björn
Laurell, Thomas
Fröbert, Ole
Erlinge, David
Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial Vesiculation
title Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial Vesiculation
title_full Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial Vesiculation
title_fullStr Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial Vesiculation
title_full_unstemmed Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial Vesiculation
title_short Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial Vesiculation
title_sort bilberry supplementation after myocardial infarction decreases microvesicles in blood and affects endothelial vesiculation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685140/
https://www.ncbi.nlm.nih.gov/pubmed/32846041
http://dx.doi.org/10.1002/mnfr.202000108
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