Antioxidant Effects of a Hydroxytyrosol-Based Pharmaceutical Formulation on Body Composition, Metabolic State, and Gene Expression: A Randomized Double-Blinded, Placebo-Controlled Crossover Trial.
Antioxidant Effects of a Hydroxytyrosol-Based Pharmaceutical Formulation on Body Composition, Metabolic State, and Gene Expression: A Randomized Double-Blinded, Placebo-Controlled Crossover Trial.
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基于羟基羟基醇的药物配方对人体组成,代谢状态和基因表达的抗氧化作用:一项随机的双盲,安慰剂对照的交叉试验。
DOI:
10.1155/2017/2473495
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发表时间:
2017
影响因子:
--
通讯作者:
De Lorenzo A
中科院分区:
文献类型:
--
作者:
Colica C;Di Renzo L;Trombetta D;Smeriglio A;Bernardini S;Cioccoloni G;Costa de Miranda R;Gualtieri P;Sinibaldi Salimei P;De Lorenzo A
Hydroxytyrosol (HT) plays a significant role in cardiovascular disease (CVD) protection, and its metabolites are able to protect from the endothelial dysfunction commonly present in atherosclerosis. This randomized double-blinded, placebo-controlled crossover trial determined the effect in healthy volunteers of two gastroresistant capsules containing 15 mg/day of HT, for a 3-week period (HTT). Evaluation of nutritional status, serum metabolites, oxidative stress biomarkers, and gene expression of 9 genes related to oxidative stress, inflammation, and CVDs was performed. Oxidation biomarkers like thiol group (p = 0.001), total antioxidant status (TAS) (p = 0.001), superoxide dismutase 1 (SOD1) (2−ΔΔCt = 3.7), and plasma concentration of HT (2.83 μg·mL−1) were significantly increased, while nitrite (p = 0.001), nitrate (p = 0.001), and malondialdehyde (MDA) (p = 0.02) were drastically reduced after HTT. A significant reduction of body fat mass percentage (p = 0.01), suprailiac skinfold (p = 0.01), and weight (p = 0.04; Δ% = −0.46%) was observed after HTT. This study shows that regular intake of 15 mg/day of HT changed body composition parameters and modulated the antioxidant profile and the expression of inflammation and oxidative stress-related genes. However, it is advisable to personalize HT doses in order to exert its health benefits in CVD prevention and protection of LDL-C particles from oxidative damage. This trial is registered with ClinicalTrials.gov NCT01890070.
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影响因子:
5.6
作者:
D'Archivio M;Filesi C;Varì R;Scazzocchio B;Masella R
通讯作者:
Masella R
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3.3
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Verhagen, Hans
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de la Torre, R
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de la Puerta, R;Domínguez, MEM;Hoult, JRS
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Hoult, JRS
影响因子:
7.1
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Bouwens, Mark;Afman, Lydia A.;Muller, Michael
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Muller, Michael