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The Sustained Delivery of Resveratrol or a Defined Grape Powder Inhibits New Blood Vessel Formation in a Mouse Model of Choroidal Neovascularization

The objective of this study was to determine whether resveratrol or a defined, reconstituted grape powder can attenuate the formation of new blood vessels in a mouse model of choroidal neovascularization (CNV). To accomplish this objective, C57BL/6J mice were randomized into control or treatment gro...

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Autores principales: Kanavi, Mozhgan Rezaie, Darjatmoko, Soesiawati, Wang, Shoujian, Azari, Amir A., Farnoodian, Mitra, Kenealey, Jason D., van Ginkel, Paul R., Albert, Daniel M., Sheibani, Nader, Polans, Arthur S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313391/
https://www.ncbi.nlm.nih.gov/pubmed/25361423
http://dx.doi.org/10.3390/molecules191117578
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author Kanavi, Mozhgan Rezaie
Darjatmoko, Soesiawati
Wang, Shoujian
Azari, Amir A.
Farnoodian, Mitra
Kenealey, Jason D.
van Ginkel, Paul R.
Albert, Daniel M.
Sheibani, Nader
Polans, Arthur S.
author_facet Kanavi, Mozhgan Rezaie
Darjatmoko, Soesiawati
Wang, Shoujian
Azari, Amir A.
Farnoodian, Mitra
Kenealey, Jason D.
van Ginkel, Paul R.
Albert, Daniel M.
Sheibani, Nader
Polans, Arthur S.
author_sort Kanavi, Mozhgan Rezaie
collection PubMed
description The objective of this study was to determine whether resveratrol or a defined, reconstituted grape powder can attenuate the formation of new blood vessels in a mouse model of choroidal neovascularization (CNV). To accomplish this objective, C57BL/6J mice were randomized into control or treatment groups which received either resveratrol or grape powder by daily oral gavage, resveratrol or grape powder delivered ad libitum through the drinking water, or resveratrol by slow release via implanted osmotic pumps. A laser was used to rupture Bruch’s membrane to induce CNV which was then detected in sclerochoroidal eyecups stained with antibodies against intercellular adhesion molecule-2. CNV area was measured using fluorescence microscopy and Image J software. Ad libitum delivery of both resveratrol and grape powder was shown to significantly reduce the extent of CNV by 68% and 57%, respectively. Parallel experiments conducted in vitro demonstrated that resveratrol activates p53 and inactivates Akt/protein kinase B in choroidal endothelial cells, contributing to its anti-proliferative and anti-migratory properties. In addition resveratrol was shown to inhibit the formation of endothelial cell networks, augmenting its overall anti-angiogenic effects. The non-toxic nature of resveratrol makes it an especially attractive candidate for the prevention and/or treatment of CNV.
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spelling pubmed-43133912015-10-30 The Sustained Delivery of Resveratrol or a Defined Grape Powder Inhibits New Blood Vessel Formation in a Mouse Model of Choroidal Neovascularization Kanavi, Mozhgan Rezaie Darjatmoko, Soesiawati Wang, Shoujian Azari, Amir A. Farnoodian, Mitra Kenealey, Jason D. van Ginkel, Paul R. Albert, Daniel M. Sheibani, Nader Polans, Arthur S. Molecules Article The objective of this study was to determine whether resveratrol or a defined, reconstituted grape powder can attenuate the formation of new blood vessels in a mouse model of choroidal neovascularization (CNV). To accomplish this objective, C57BL/6J mice were randomized into control or treatment groups which received either resveratrol or grape powder by daily oral gavage, resveratrol or grape powder delivered ad libitum through the drinking water, or resveratrol by slow release via implanted osmotic pumps. A laser was used to rupture Bruch’s membrane to induce CNV which was then detected in sclerochoroidal eyecups stained with antibodies against intercellular adhesion molecule-2. CNV area was measured using fluorescence microscopy and Image J software. Ad libitum delivery of both resveratrol and grape powder was shown to significantly reduce the extent of CNV by 68% and 57%, respectively. Parallel experiments conducted in vitro demonstrated that resveratrol activates p53 and inactivates Akt/protein kinase B in choroidal endothelial cells, contributing to its anti-proliferative and anti-migratory properties. In addition resveratrol was shown to inhibit the formation of endothelial cell networks, augmenting its overall anti-angiogenic effects. The non-toxic nature of resveratrol makes it an especially attractive candidate for the prevention and/or treatment of CNV. MDPI 2014-10-30 /pmc/articles/PMC4313391/ /pubmed/25361423 http://dx.doi.org/10.3390/molecules191117578 Text en © 2014 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kanavi, Mozhgan Rezaie
Darjatmoko, Soesiawati
Wang, Shoujian
Azari, Amir A.
Farnoodian, Mitra
Kenealey, Jason D.
van Ginkel, Paul R.
Albert, Daniel M.
Sheibani, Nader
Polans, Arthur S.
The Sustained Delivery of Resveratrol or a Defined Grape Powder Inhibits New Blood Vessel Formation in a Mouse Model of Choroidal Neovascularization
title The Sustained Delivery of Resveratrol or a Defined Grape Powder Inhibits New Blood Vessel Formation in a Mouse Model of Choroidal Neovascularization
title_full The Sustained Delivery of Resveratrol or a Defined Grape Powder Inhibits New Blood Vessel Formation in a Mouse Model of Choroidal Neovascularization
title_fullStr The Sustained Delivery of Resveratrol or a Defined Grape Powder Inhibits New Blood Vessel Formation in a Mouse Model of Choroidal Neovascularization
title_full_unstemmed The Sustained Delivery of Resveratrol or a Defined Grape Powder Inhibits New Blood Vessel Formation in a Mouse Model of Choroidal Neovascularization
title_short The Sustained Delivery of Resveratrol or a Defined Grape Powder Inhibits New Blood Vessel Formation in a Mouse Model of Choroidal Neovascularization
title_sort sustained delivery of resveratrol or a defined grape powder inhibits new blood vessel formation in a mouse model of choroidal neovascularization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313391/
https://www.ncbi.nlm.nih.gov/pubmed/25361423
http://dx.doi.org/10.3390/molecules191117578
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