Bilberry Supplementation after Myocardial Infarction Decreases Microvesicles in Blood and Affects Endothelial VesiculationShow others and affiliations
2020 (English)In: Molecular Nutrition & Food Research, ISSN 1613-4125, E-ISSN 1613-4133, Vol. 64, no 20, article id e2000108Article in journal (Refereed) Published
Abstract [en]
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.
Place, publisher, year, edition, pages
Wiley-VCH Verlagsgesellschaft, 2020. Vol. 64, no 20, article id e2000108
Keywords [en]
bilberries, cardiovascular diseases, microvesicles, P2X7 (P2X purinorecep-tor 7)
National Category
Cardiology and Cardiovascular Disease Nutrition and Dietetics
Identifiers
URN: urn:nbn:se:oru:diva-85332DOI: 10.1002/mnfr.202000108ISI: 000567543700001PubMedID: 32846041Scopus ID: 2-s2.0-85090439473OAI: oai:DiVA.org:oru-85332DiVA, id: diva2:1465083
Funder
Swedish Foundation for Strategic Research Knut and Alice Wallenberg FoundationSwedish Heart Lung FoundationSwedish Research Council
Note
Funding Agencies:
Region of Scania
ALF-funds
2020-09-082020-09-082025-02-11Bibliographically approved