Lanningham-Foster L, Chen C, Chance D S, Loo G
Department of Food, Nutrition and Food Service Management, School of Human Environmental Sciences, University of North Carolina, Greensboro 27412-5001, USA.
Biol Pharm Bull. 1995 Oct;18(10):1347-51. doi: 10.1248/bpb.18.1347.
Some epidemiological data have linked dietary polyphenols with lower risk of coronary heart disease. Polyphenols might impair lipoprotein oxidation which is believed to be an important step in initiating atherogenesis. The purpose of this study was to determine if grape extract known to contain polyphenolic substances can block copper-induced oxidative modification of human low density lipoprotein (LDL).LDL oxidation was monitored spectrophotometrically by measurement of change in absorbance at 234 nm. Incubation of LDL (0.05 mg protein/ml) with 1.66 microM cupric chloride produced a lag phase of 130 min before onset of the propagation phase where polyunsaturated fatty acids undergo conversion to conjugated lipid hydroperoxides. However, in the presence of grape extract at a final concentration equal to an 8000-fold dilution, the lag phase was extended to 185 min. A 4000-fold and 2000-fold dilution of grape extract produced lag phases of 250 and 465 min, respectively. LDL oxidation was essentially blocked for at least 10 h with a 1000-fold dilution of grape extract. In other experiments, incubation of LDL (0.2 mg protein/ml) with 5 microM cupric chloride for 1-4 h increased both thiobarbituric acid-reactive substances and electrophoretic mobility of LDL on agarose gel. In addition, there was loss of immunoreactivity of LDL with a murine monoclonal antibody against human apolipoprotein B-100. However, these oxidative changes to LDL by copper were prevented when diluted grape extract was present during incubation. It is concluded that grape extract contains antioxidants in the form of polyphenols with the capacity to inhibit oxidative modification of LDL.
一些流行病学数据表明,膳食多酚与降低冠心病风险有关。多酚可能会抑制脂蛋白氧化,而脂蛋白氧化被认为是引发动脉粥样硬化的重要步骤。本研究的目的是确定已知含有多酚类物质的葡萄提取物是否能阻止铜诱导的人低密度脂蛋白(LDL)的氧化修饰。通过测量234nm处吸光度的变化,用分光光度法监测LDL氧化。将LDL(0.05mg蛋白质/ml)与1.66μM氯化铜孵育,在多不饱和脂肪酸转化为共轭脂质氢过氧化物的增殖阶段开始前,有130分钟的延迟期。然而,在最终浓度相当于8000倍稀释的葡萄提取物存在下,延迟期延长至185分钟。葡萄提取物4000倍和2000倍稀释分别产生250分钟和465分钟的延迟期。用1000倍稀释的葡萄提取物,LDL氧化在至少10小时内基本被阻断。在其他实验中,将LDL(0.2mg蛋白质/ml)与5μM氯化铜孵育1-4小时,会增加硫代巴比妥酸反应性物质以及LDL在琼脂糖凝胶上的电泳迁移率。此外,LDL与抗人载脂蛋白B-100的鼠单克隆抗体的免疫反应性丧失。然而,在孵育过程中存在稀释的葡萄提取物时,铜对LDL的这些氧化变化被阻止。结论是葡萄提取物含有多酚形式的抗氧化剂,具有抑制LDL氧化修饰的能力。