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Modifying Choroidal Neovascularization Development with a Nutritional Supplement in Mice

We examined the effect of nutritional supplements (modified Age Related Eye Disease Study (AREDS)-II formulation containing vitamins, minerals, lutein, resveratrol, and omega-3 fatty acids) on choroidal neovascularization (CNV). Supplements were administered alone and combined with intravitreal anti...

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Autores principales: Ivanescu, Alina Adriana, Fernández-Robredo, Patricia, Heras-Mulero, Henar, Sádaba-Echarri, Luis Manuel, García-García, Laura, Fernández-García, Vanessa, Moreno-Orduna, Maite, Redondo-Exposito, Aitor, Recalde, Sergio, García-Layana, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517006/
https://www.ncbi.nlm.nih.gov/pubmed/26153682
http://dx.doi.org/10.3390/nu7075229
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author Ivanescu, Alina Adriana
Fernández-Robredo, Patricia
Heras-Mulero, Henar
Sádaba-Echarri, Luis Manuel
García-García, Laura
Fernández-García, Vanessa
Moreno-Orduna, Maite
Redondo-Exposito, Aitor
Recalde, Sergio
García-Layana, Alfredo
author_facet Ivanescu, Alina Adriana
Fernández-Robredo, Patricia
Heras-Mulero, Henar
Sádaba-Echarri, Luis Manuel
García-García, Laura
Fernández-García, Vanessa
Moreno-Orduna, Maite
Redondo-Exposito, Aitor
Recalde, Sergio
García-Layana, Alfredo
author_sort Ivanescu, Alina Adriana
collection PubMed
description We examined the effect of nutritional supplements (modified Age Related Eye Disease Study (AREDS)-II formulation containing vitamins, minerals, lutein, resveratrol, and omega-3 fatty acids) on choroidal neovascularization (CNV). Supplements were administered alone and combined with intravitreal anti-VEGF in an early-CNV (diode laser-induced) murine model. Sixty mice were evenly divided into group V (oral vehicle, intravitreal saline), group S (oral supplement, intravitreal saline), group V + aVEGF (oral vehicle, intravitreal anti-VEGF), and group S + aVEGF (oral supplement, intravitreal anti-VEGF). Vehicle and nutritional supplements were administered daily for 38 days beginning 10 days before laser. Intravitreal injections were administered 48 h after laser. Fluorescein angiography (FA) and flat-mount CD31 staining evaluated leakage and CNV lesion area. Expression of VEGF, MMP-2 and MMP-9 activity, and NLRP3 were evaluated with RT-PCR, zymography, and western-blot. Leakage, CNV size, VEGF gene and protein expression were lower in groups V + aVEGF, S + aVEGF, and S than in V (all p < 0.05). Additionally, MMP-9 gene expression differed between groups S + aVEGF and V (p < 0.05) and MMP-9 activity was lower in S + aVEGF than in V and S (both p < 0.01). Levels of MMP-2 and NLRP3 were not significantly different between groups. Nutritional supplements either alone or combined with anti-VEGF may mitigate CNV development and inhibit retinal disease involving VEGF overexpression and CNV.
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spelling pubmed-45170062015-07-30 Modifying Choroidal Neovascularization Development with a Nutritional Supplement in Mice Ivanescu, Alina Adriana Fernández-Robredo, Patricia Heras-Mulero, Henar Sádaba-Echarri, Luis Manuel García-García, Laura Fernández-García, Vanessa Moreno-Orduna, Maite Redondo-Exposito, Aitor Recalde, Sergio García-Layana, Alfredo Nutrients Article We examined the effect of nutritional supplements (modified Age Related Eye Disease Study (AREDS)-II formulation containing vitamins, minerals, lutein, resveratrol, and omega-3 fatty acids) on choroidal neovascularization (CNV). Supplements were administered alone and combined with intravitreal anti-VEGF in an early-CNV (diode laser-induced) murine model. Sixty mice were evenly divided into group V (oral vehicle, intravitreal saline), group S (oral supplement, intravitreal saline), group V + aVEGF (oral vehicle, intravitreal anti-VEGF), and group S + aVEGF (oral supplement, intravitreal anti-VEGF). Vehicle and nutritional supplements were administered daily for 38 days beginning 10 days before laser. Intravitreal injections were administered 48 h after laser. Fluorescein angiography (FA) and flat-mount CD31 staining evaluated leakage and CNV lesion area. Expression of VEGF, MMP-2 and MMP-9 activity, and NLRP3 were evaluated with RT-PCR, zymography, and western-blot. Leakage, CNV size, VEGF gene and protein expression were lower in groups V + aVEGF, S + aVEGF, and S than in V (all p < 0.05). Additionally, MMP-9 gene expression differed between groups S + aVEGF and V (p < 0.05) and MMP-9 activity was lower in S + aVEGF than in V and S (both p < 0.01). Levels of MMP-2 and NLRP3 were not significantly different between groups. Nutritional supplements either alone or combined with anti-VEGF may mitigate CNV development and inhibit retinal disease involving VEGF overexpression and CNV. MDPI 2015-07-06 /pmc/articles/PMC4517006/ /pubmed/26153682 http://dx.doi.org/10.3390/nu7075229 Text en © 2015 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
Ivanescu, Alina Adriana
Fernández-Robredo, Patricia
Heras-Mulero, Henar
Sádaba-Echarri, Luis Manuel
García-García, Laura
Fernández-García, Vanessa
Moreno-Orduna, Maite
Redondo-Exposito, Aitor
Recalde, Sergio
García-Layana, Alfredo
Modifying Choroidal Neovascularization Development with a Nutritional Supplement in Mice
title Modifying Choroidal Neovascularization Development with a Nutritional Supplement in Mice
title_full Modifying Choroidal Neovascularization Development with a Nutritional Supplement in Mice
title_fullStr Modifying Choroidal Neovascularization Development with a Nutritional Supplement in Mice
title_full_unstemmed Modifying Choroidal Neovascularization Development with a Nutritional Supplement in Mice
title_short Modifying Choroidal Neovascularization Development with a Nutritional Supplement in Mice
title_sort modifying choroidal neovascularization development with a nutritional supplement in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517006/
https://www.ncbi.nlm.nih.gov/pubmed/26153682
http://dx.doi.org/10.3390/nu7075229
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