Gopaul N K, Nourooz-Zadeh J, Mallet A I, Anggård E E
William Harvey Research Institute, St. Batholomew's Hospital Medical College, London, UK.
Biochem Biophys Res Commun. 1994 Apr 15;200(1):338-43. doi: 10.1006/bbrc.1994.1453.
It has been recently reported that a series of prostaglandin F2-like compounds (PGF2-isoprostanes) are produced in vivo by non-enzymatic peroxidation of arachidonic acid. Of these, 8-epi-PGF2 alpha is the major component and has been shown to be a potent vasoconstrictor. Here we investigated the formation of PGF2-isoprostanes during copper-mediated oxidation of low density lipoprotein (LDL). Free and total (sum of free and esterified) levels of PGF2-isoprostanes were measured at times 0, 3, 6, 8 and 24 h, using a solid-phase extraction procedure and gas chromatography-mass spectrometry. In native LDL, free levels of PGF2-isoprostanes were between 0.06 and 0.10 ng/mg protein (n = 4), and the total levels ranged from 0.027 to 0.057 ng/mg protein (n = 4). Free levels of the isoprostanes were found to increase throughout the oxidation, whereas total levels reached a maximum after 3 h then gradually decreased. 8-epi-PGF2 alpha was the major isoprostane formed (free concentration after 24 h 1.8 +/- 0.1 ng/mg protein (n = 4); total concentrations of 8.8 +/- 1.8 and 6.1 +/- 3.6 ng/mg protein (n = 4) after 3 and 24 h, respectively). The levels of isoprostanes correlated well with other indices of lipid peroxidation (conjugated dienes, hydroperoxides, thiobarbituric reactive substances) measured at similar time points. The release of PGF2-isoprostanes from oxidised LDL in macrophages could be a contributory factor in the development of atherosclerosis.
最近有报道称,一系列前列腺素F2样化合物(PGF2-异前列腺素)在体内由花生四烯酸的非酶促过氧化反应产生。其中,8-表-PGF2α是主要成分,并且已被证明是一种有效的血管收缩剂。在此,我们研究了低密度脂蛋白(LDL)铜介导氧化过程中PGF2-异前列腺素的形成。使用固相萃取程序和气相色谱-质谱法,在0、3、6、8和24小时测量PGF2-异前列腺素的游离水平和总水平(游离和酯化的总和)。在天然LDL中,PGF2-异前列腺素的游离水平在0.06至0.10 ng/mg蛋白质之间(n = 4),总水平在0.027至0.057 ng/mg蛋白质之间(n = 4)。发现异前列腺素的游离水平在整个氧化过程中增加,而总水平在3小时后达到最大值,然后逐渐下降。8-表-PGF2α是形成的主要异前列腺素(24小时后游离浓度为1.8±0.1 ng/mg蛋白质(n = 4);3小时和24小时后8-表-PGF2α的总浓度分别为8.8±1.8和6.1±3.6 ng/mg蛋白质(n = 4))。异前列腺素的水平与在相似时间点测量的其他脂质过氧化指标(共轭二烯、氢过氧化物、硫代巴比妥酸反应性物质)密切相关。巨噬细胞中氧化LDL释放的PGF2-异前列腺素可能是动脉粥样硬化发展的一个促成因素。