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Elevation of free Fatty acids induces inflammation and impairs vascular reactivity in healthy subjects.

机译:游离脂肪酸的升高会诱发健康受试者的炎症并损害血管反应性。

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To test the possible acute proinflammatory effects of fatty acids, we induced an increase in plasma free fatty acid (FFA) concentrations after a lipid and heparin infusion for 4 h in 10 healthy subjects. We determined the nuclear factor-kappaB (NF-kappaB) binding activity in mononuclear cells (MNCs), the p65 subunit of NF-kappaB, reactive oxygen species (ROS) generation by MNC, and polymorphonuclear leukocytes (PMN). Brachial artery reactivity, using postischemic flow-mediated dilation, was also measured. NF-kappaB binding activity in the MNC nuclear extracts increased to 163 +/- 17% and 144 +/- 14% as compared with basal levels at 2 and 4 h (P < 0.005) and remained elevated (P < 0.05) at 6 h (2 h after cessation of lipid infusion). NF-kappaB p65 subunit protein expression in MNC homogenates also increased at 2, 4, and 6 h (P < 0.05). ROS generation by PMNs increased significantly at 2 and 4 h (P < 0.005), whereas that by MNCs increased at 4 h (P < 0.05). Plasma macrophage migration inhibitory factor increased at 2 (P < 0.05) and 4 h (P < 0.005), respectively, and declined to baseline at 6 h. The postischemic flow-mediated dilation of brachial artery decreased from 6.3 +/- 1.1% at baseline to 4.3 +/- 1.9% and 2.7 +/- 2.1% (P < 0.01) at 2, 4, and 6 h, respectively. We conclude that an increase in FFA concentration induces oxidative stress and has a proinflammatory effect; it also impairs postischemic flow-mediated vasodilation of the brachial artery.
机译:为了测试脂肪酸可能的急性促炎作用,我们在10名健康受试者中注入脂质和肝素4小时后,血浆游离脂肪酸(FFA)浓度增加。我们确定了单核细胞(MNC)中的核因子-κB(NF-kappaB)结合活性,NF-kappaB的p65亚基,MNC产生的活性氧(ROS)和多形核白细胞(PMN)。还测量了缺血后血流介导的扩张的肱动脉反应性。与第2小时和第4小时的基础水平相比,MNC核提取物中的NF-κB结合活性增加至163 +/- 17%和144 +/- 14%(P <0.005),并在6时仍保持升高(P <0.05)小时(停止输注脂质后2小时)。 MNC匀浆中的NF-κBp65亚基蛋白表达在第2、4和6小时也增加(P <0.05)。 PMN的ROS生成在2和4 h时显着增加(P <0.005),而MNC的ROS在4 h时增加(P <0.05)。血浆巨噬细胞迁移抑制因子分别在第2 h(P <0.05)和第4 h(P <0.005)升高,在第6 h降至基线。肱动脉缺血后血流介导的扩张从基线时的6.3 +/- 1.1%分别降至2、4和6 h时的4.3 +/- 1.9%和2.7 +/- 2.1%(P <0.01)。我们得出的结论是,FFA浓度的增加会诱导氧化应激并具有促炎作用。它还损害了缺血后血流介导的肱动脉血管舒张。

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