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Anti-Atherosclerotic Effect of a Polyphenol-Rich Ingredient, Oleactiv(®), in a Hypercholesterolemia-Induced Golden Syrian Hamster Model

The development of nutraceutical ingredients has risen as a nutritional solution for health prevention. This study evaluated the effects of Oleactiv(®), an ingredient developed for the prevention of atherogenesis, in hypercholesterolemic hamsters. Oleactiv(®) is a polyphenol-rich ingredient obtained...

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Autores principales: Romain, Cindy, Piemontese, Antonio, Battista, Simone, Bernini, Franco, Ossoli, Alice, Strazzella, Arianna, Gaillet, Sylvie, Rouanet, Jean-Max, Cases, Julien, Zanotti, Ilaria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213376/
https://www.ncbi.nlm.nih.gov/pubmed/30326655
http://dx.doi.org/10.3390/nu10101511
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author Romain, Cindy
Piemontese, Antonio
Battista, Simone
Bernini, Franco
Ossoli, Alice
Strazzella, Arianna
Gaillet, Sylvie
Rouanet, Jean-Max
Cases, Julien
Zanotti, Ilaria
author_facet Romain, Cindy
Piemontese, Antonio
Battista, Simone
Bernini, Franco
Ossoli, Alice
Strazzella, Arianna
Gaillet, Sylvie
Rouanet, Jean-Max
Cases, Julien
Zanotti, Ilaria
author_sort Romain, Cindy
collection PubMed
description The development of nutraceutical ingredients has risen as a nutritional solution for health prevention. This study evaluated the effects of Oleactiv(®), an ingredient developed for the prevention of atherogenesis, in hypercholesterolemic hamsters. Oleactiv(®) is a polyphenol-rich ingredient obtained from artichoke, olive and grape extracts as part of fruit and vegetables commonly consumed within the Mediterranean diet. A total of 21 Golden Syrian hamsters were divided into three groups. The standard group (STD) was fed a normolipidemic diet for 12 weeks, while the control group (CTRL) and Oleactiv(®) goup (OLE) were fed a high-fat diet. After sacrifice, the aortic fatty streak area (AFSA), plasmatic total cholesterol (TC), high-density lipoproteins (HDL-C), non-HDL-C and triglycerides (TG), were assessed. The cholesterol efflux capacity (CEC) of hamster plasma was quantified using a radiolabeled technique in murine macrophages J774. OLE administration induced a significant reduction of AFSA (−69%, p < 0.0001). Hamsters of the OLE group showed a significant decrease of both non-HDL-C (−173 mmol/L, p < 0.05) and TG (−154 mmol/L, p < 0.05). Interestingly, OLE induced a significant increase of total CEC (+17,33%, p < 0,05). Oleactiv(®) supplementation prevented atheroma development and had positive effects on the lipid profile of hypercholesterolemic hamsters. The increased CEC underlines the anti-atherosclerotic mechanism at the root of the atheroma reduction observed.
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spelling pubmed-62133762018-11-06 Anti-Atherosclerotic Effect of a Polyphenol-Rich Ingredient, Oleactiv(®), in a Hypercholesterolemia-Induced Golden Syrian Hamster Model Romain, Cindy Piemontese, Antonio Battista, Simone Bernini, Franco Ossoli, Alice Strazzella, Arianna Gaillet, Sylvie Rouanet, Jean-Max Cases, Julien Zanotti, Ilaria Nutrients Article The development of nutraceutical ingredients has risen as a nutritional solution for health prevention. This study evaluated the effects of Oleactiv(®), an ingredient developed for the prevention of atherogenesis, in hypercholesterolemic hamsters. Oleactiv(®) is a polyphenol-rich ingredient obtained from artichoke, olive and grape extracts as part of fruit and vegetables commonly consumed within the Mediterranean diet. A total of 21 Golden Syrian hamsters were divided into three groups. The standard group (STD) was fed a normolipidemic diet for 12 weeks, while the control group (CTRL) and Oleactiv(®) goup (OLE) were fed a high-fat diet. After sacrifice, the aortic fatty streak area (AFSA), plasmatic total cholesterol (TC), high-density lipoproteins (HDL-C), non-HDL-C and triglycerides (TG), were assessed. The cholesterol efflux capacity (CEC) of hamster plasma was quantified using a radiolabeled technique in murine macrophages J774. OLE administration induced a significant reduction of AFSA (−69%, p < 0.0001). Hamsters of the OLE group showed a significant decrease of both non-HDL-C (−173 mmol/L, p < 0.05) and TG (−154 mmol/L, p < 0.05). Interestingly, OLE induced a significant increase of total CEC (+17,33%, p < 0,05). Oleactiv(®) supplementation prevented atheroma development and had positive effects on the lipid profile of hypercholesterolemic hamsters. The increased CEC underlines the anti-atherosclerotic mechanism at the root of the atheroma reduction observed. MDPI 2018-10-15 /pmc/articles/PMC6213376/ /pubmed/30326655 http://dx.doi.org/10.3390/nu10101511 Text en © 2018 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Romain, Cindy
Piemontese, Antonio
Battista, Simone
Bernini, Franco
Ossoli, Alice
Strazzella, Arianna
Gaillet, Sylvie
Rouanet, Jean-Max
Cases, Julien
Zanotti, Ilaria
Anti-Atherosclerotic Effect of a Polyphenol-Rich Ingredient, Oleactiv(®), in a Hypercholesterolemia-Induced Golden Syrian Hamster Model
title Anti-Atherosclerotic Effect of a Polyphenol-Rich Ingredient, Oleactiv(®), in a Hypercholesterolemia-Induced Golden Syrian Hamster Model
title_full Anti-Atherosclerotic Effect of a Polyphenol-Rich Ingredient, Oleactiv(®), in a Hypercholesterolemia-Induced Golden Syrian Hamster Model
title_fullStr Anti-Atherosclerotic Effect of a Polyphenol-Rich Ingredient, Oleactiv(®), in a Hypercholesterolemia-Induced Golden Syrian Hamster Model
title_full_unstemmed Anti-Atherosclerotic Effect of a Polyphenol-Rich Ingredient, Oleactiv(®), in a Hypercholesterolemia-Induced Golden Syrian Hamster Model
title_short Anti-Atherosclerotic Effect of a Polyphenol-Rich Ingredient, Oleactiv(®), in a Hypercholesterolemia-Induced Golden Syrian Hamster Model
title_sort anti-atherosclerotic effect of a polyphenol-rich ingredient, oleactiv(®), in a hypercholesterolemia-induced golden syrian hamster model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213376/
https://www.ncbi.nlm.nih.gov/pubmed/30326655
http://dx.doi.org/10.3390/nu10101511
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