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Title

Hydroxytyrosol administration enhances atherosclerotic lesion development in apo E deficient mice

AuthorsAcín, Sergio; Navarro, María Ángeles; Arbonés-Mainar, José M.; Guillén, Natalia; Sarría, Alfonso J.; Carnicer, Ricardo; Surra, Joaquín C.; Orman, Israel; Segovia, José Carlos; Torre, Rafael de la; Covas, María Isabel; Fernández-Bolaños Guzmán, Juan ; Ruiz-Gutiérrez, Valentina ; Osada, Jesús
KeywordsAtherosclerosis
Hydroxytyrosol
Lipoproteins
Olive oil
Transgenic animal
Issue DateSep-2006
PublisherJapanese Biochemical Society
CitationJournal of Biochemistry 140(3): 383-391 (2006)
AbstractHydroxytyrosol is a phenol found in olive oil. To verify the effect of hydroxytyrosol on the development of atherosclerosis, two groups of apo E deficient male mice on a standard chow diet were used: the control group receiving only water, and the second group an aqueous solution of hydroxytyrosol in order to provide a dose of 10 mg/kg/day to each mouse. This treatment was maintained for 10 weeks. At the moment of sacrifice, blood was drawn and heart removed. Plasma lipids, apolipoproteins and monocyte Mac-1 expression were assayed as well as aortic atherosclerotic areas in both groups. Data showed no significant changes in HDL cholesterol, paraoxonase, apolipoprotein B or triglyceride levels. However, hydroxytyrosol administration decreased apolipoprotein A-I and increased total cholesterol, atherosclerotic lesion areas and circulating monocytes expressing Mac-1. The latter was highly correlated with lesion areas (r = 0.65, P < 0.01). These results indicate that administration of hydroxytyrosol in low cholesterol diets increases atherosclerotic lesion associated with the degree of monocyte activation and remodelling of plasma lipoproteins. Our data supports the concept that phenolic-enriched products, out of the original matrix, could be not only non useful but also harmful. Our results suggest that the formulation of possible functional foods should approximate as much as possible the natural environment in which active molecules are found.
Publisher version (URL)http://dx.doi.org/10.1093/jb/mvj166
URIhttp://hdl.handle.net/10261/55693
DOI10.1093/jb/mvj166
ISSN1756-2651
E-ISSN0021-924X
Appears in Collections:(IG) Artículos
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