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Serum Lipid and Blood Pressure Responses to Quercetin Vary in Overweight Patients by Apolipoprotein E Genotype

机译:载脂蛋白E基因型对超重患者血清脂质和血压的变化对槲皮素的影响

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摘要

Our objective was to examine the effect of a quercetin supplementation on blood pressure, lipid metabolism, markers of oxidative stress, inflammation, and body composition in an at-risk population of 93 overweight-obese volunteers aged 25–65 y with metabolic syndrome traits in relation to apolipoprotein (apo) E genotype. Participants were randomized to receive 150 mg/d quercetin in a double-blinded, placebo-controlled, crossover trial with 6-wk treatment periods separated by a 5-wk washout period. Retrospectively, 5 apoE genotype variants were found (2/3, n = 3; 3/3, n = 60; 3/4, n = 23; 2/4, n = 4; and 4/4, n = 3). Participants were classified into the following 3 apoE phenotypes: apoE2 (n = 3), apoE3 (n = 60), and apoE4 (n = 26). Data were analyzed for apoE3 and apoE4 subgroups. Quercetin decreased systolic blood pressure by 3.4 mm Hg (P < 0.01) in the apoE3 group, whereas no significant effect was observed in the apoE4 group. Quercetin decreased serum HDL cholesterol (P < 0.01) and apoA1 (P sup> 0.01) and increased the LDL:HDL cholesterol ratio (P < 0.05) in the apoE4 subgroup, whereas the apoE3 subgroup had no significant changes in these variables. Quercetin significantly decreased plasma oxidized LDL and tumor necrosis factor- in the apoE3 and apoE4 groups, whereas no significant inter-group differences were found. Serum C-reactive protein and nutritional status (body weight, waist circumference, fat mass, fat-free mass) were unaffected compared with placebo. In conclusion, quercetin exhibited blood pressure-lowering effects in overweight-obese carriers of the apo 3/3 genotype but not in carriers of the 4 allele. Furthermore, quercetin supplementation resulted in a reduction in HDL cholesterol and apoA1 in apo 4 carriers.
机译:我们的目标是检查高危人群中补充槲皮素 对血压,脂质代谢,氧化应激指标, 炎症和身体成分的影响。 > 93位年龄在25-65岁之间,具有与载脂蛋白(apo)E基因型相关的代谢 综合征特征的超重志愿者。 参与者被随机分配接受150例mg / d槲皮素在 一项双盲,安慰剂对照,交叉试验中,治疗期为6周 ,间隔为5周。回顾性地发现了 5个apoE基因型变异(2/3,n = 3; 3/3,n = 60; 3/4,n = 23; 2/4 ,n = 4;和4/4,n = 3)。参与者被 分为以下3种apoE表型:apoE2(n = 3),apoE3(n = 60)和apoE4(n = 26)。分析了 apoE3和apoE4子组的数据。槲皮素在apoE3组中使收缩压降低3.4 mm Hg(P <0.01),而在apoE4组中未观察到显着影响。槲皮素 降低血清HDL胆固醇(P <0.01)和apoA1(P sup> 0.01)并增加LDL:HDL胆固醇比率(P <0.05) 在apoE4子组中,而apoE3子组在这些变量中没有显着的 变化。在apoE3 和apoE4组中,槲皮素显着降低了 血浆氧化的LDL和肿瘤坏死因子-,而未发现显着的组间差异 。与安慰剂相比,血清C反应蛋白和营养状况(体重,腰围,脂肪量,无脂肪量) 未受影响。总之,槲皮素 在apo 3/3基因型的超重肥胖 携带者中表现出降压作用,但在 4携带者中却没有表现出降血压作用等位基因。此外,槲皮素的补充导致apo 4携带者的 降低HDL胆固醇和apoA1。

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  • 来源
    《Journal of Nutrition》 |2010年第2期|278-284|共7页
  • 作者单位

    Institute of Nutrition and Food Science, Nutritional Physiology, University of Bonn, 53115 Bonn, Germany|Department of Human Nutrition, Institute of Human Nutrition and Food Science, Christian-Albrechts-University Kiel, 24105 Kiel, Germany;

    Department of Food Science, Institute of Human Nutrition and Food Science, Christian-Albrechts-University Kiel, 24098 Kiel, Germany;

    Institute of Animal Nutrition and Physiology, Christian-Albrechts-University Kiel, 24118 Kiel, Germany;

    Department of Food Science, Institute of Human Nutrition and Food Science, Christian-Albrechts-University Kiel, 24098 Kiel, Germany;

    Department of Human Nutrition, Institute of Human Nutrition and Food Science, Christian-Albrechts-University Kiel, 24105 Kiel, Germany;

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