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首页> 外文期刊>Free radical research >Effect of aluminium on lipid peroxidation of human high density lipoproteins.
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Effect of aluminium on lipid peroxidation of human high density lipoproteins.

机译:铝对人高密度脂蛋白脂质过氧化的影响。

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We investigated the effect of aluminium (Al3+) on lipid peroxidation and physico-chemical properties of high density lipoproteins (HDL) isolated from human plasma. Our results demonstrated that Al3+ enhances lipid peroxidation of human HDL as shown by the significant increase in lipid hydroperoxides in Al-treated HDL with respect to control HDL. The oxidative effect was higher at acid pH (pH 5.5) with respect to pH 7.4. Moreover, a stimulating effect of Al3+ on iron-induced lipid peroxidation of HDL was demonstrated. The study of the effect of Al3+ on the physico-chemical properties of HDL, using the fluorescence polarization (Pf) of the probes TMA-DPH (1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene iodide) and DPH (1,6-diphenyl-1,3,5-hexatriene), showed a significant decrease of Pf in Al-treated HDL with respect to control. These results suggest that Al3+ induces a decrease of molecular order at the lipoprotein surface. Moreover, the study of tryptophan (Trp) fluorescence demonstrated that aluminium induces structural modifications of HDL apoproteins and on HDL physico-chemical properties. The effect of Al3+ on lipid peroxidation of HDL was observed at aluminium concentrations similar to those observed in the brain of patients affected by neurological diseases. Aluminium-induced oxidative damage of HDL could be involved in the development of neurological diseases.
机译:我们研究了铝(Al3 +)对从人血浆中分离的高密度脂蛋白(HDL)脂质过氧化和理化性质的影响。我们的结果表明,Al3 +增强了人类HDL的脂质过氧化作用,这是由Al处理的HDL中的脂质氢过氧化物相对于对照HDL的显着增加所表明的。相对于pH 7.4,在酸性pH(pH 5.5)下,氧化作用更高。此外,还证明了Al3 +对铁诱导的HDL脂质过氧化的刺激作用。使用探针TMA-DPH(1-(4-三甲基铵苯基)-6-苯基-1,3,5-己三碘碘化物)的荧光偏振(Pf)研究Al3 +对HDL物理化学性质的影响)和DPH(1,6-二苯基-1,3,5-己三烯)相对于对照,在Al处理的HDL中显示出Pf的显着降低。这些结果表明,Al 3+引起脂蛋白表面分子顺序的降低。此外,色氨酸(Trp)荧光的研究表明,铝诱导HDL载脂蛋白的结构修饰以及HDL的理化特性。在铝浓度下观察到Al3 +对HDL脂质过氧化的影响与在神经疾病患者的大脑中观察到的铝浓度相似。铝诱导的高密度脂蛋白的氧化损伤可能参与神经系统疾病的发展。

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