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首页> 外文期刊>The Journal of Nutrition: Official Organ of the American Institute of Nutrition >Serum Lipid and Blood Pressure Responses to Quercetin Vary in Overweight Patients by Apolipoprotein E Genotype
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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 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-α 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93名25-65岁,患有代谢综合征特征的超重志愿者的高风险人群中补充槲皮素对血压,脂质代谢,氧化应激指标,炎症和身体组成的影响。与载脂蛋白(apo)E基因型的关系。在双盲,安慰剂对照,交叉试验中,参与者随机接受150 mg / d槲皮素,治疗周期为6周,而洗脱期为5周。回顾性地发现了5个apoE基因型变异体(?2 /?3,n = 3;?3 /?3,n = 60;?3 /?4,n = 23;?2 /?4,n = 4;和?4 /?4,n = 3)。参加者分为以下3种apoE表型:apoE2(n = 3),apoE3(n = 60)和apoE4(n = 26)。分析了载脂蛋白E3和载脂蛋白E4亚组的数据。槲皮素在apoE3组中使收缩压降低了3.4 mm Hg(P <0.01),而在apoE4组中未观察到明显的作用。槲皮素降低了apoE4亚组的血清HDL胆固醇(P <0.01)和apoA1(P <0.01),并提高了LDL:HDL胆固醇比率(P <0.05),而apoE3亚组在这些变量中无显着变化。槲皮素显着降低了载脂蛋白E3和载脂蛋白E4组的血浆氧化LDL和肿瘤坏死因子-α,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,槲皮素在载脂蛋白α3/β3基因型的超重肥胖携带者中表现出降血压作用,而在β4等位基因携带者中则没有表现出降血压作用。此外,槲皮素的补充导致载脂蛋白α4携带者的HDL胆固醇和载脂蛋白A1减少。

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