Noguchi N, Gotoh N, Niki E
Research Center for Advanced Science and Technology, University of Tokyo, Japan.
Biochim Biophys Acta. 1994 Jul 14;1213(2):176-82. doi: 10.1016/0005-2760(94)90024-8.
The oxidative modification of low density lipoprotein (LDL) is accepted to be an important early event of atherosclerosis, but it has not yet been well understood. The preventive effects of two antioxidants with different functions, ebselen and probucol, against the oxidative modification of LDL induced by copper or a water-soluble radical initiator, 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) were studied in order to elucidate the mechanism of modification of apolipoprotein B-100 (apoB). Ebselen inhibited the copper-induced oxidation completely by reducing the hydroperoxides in LDL, since the initiation of copper-dependent oxidation requires the presence of a trace amount of hydroperoxides in LDL. On the other hand, ebselen did not suppress the oxidations of LDL induced by AAPH which generated free radicals by its thermal decomposition. The AAPH-induced oxidation of LDL in the absence of ebselen gave phosphatidylcholine hydroperoxide and cholesteryl ester hydroperoxide as major products, while in its presence, the hydroperoxides were reduced to corresponding alcohols. Interestingly, ebselen had little effect on the increase of relative electrophoretic mobility and fragmentation of intact apoB in the AAPH-induced oxidation. Probucol inhibited the oxidation of lipids in LDL effectively induced by either copper or AAPH, but the protein modifications were observed even in the presence of probucol. It was suggested that (1) lipid hydroperoxides do not play an important role in the modification of apoB such as increase in negative charge and fragmentation, (2) the direct attack of free radicals upon apoB and its modification by lipid oxidation products derived from hydroperoxides increase the negative charge of apoB, and (3) its fragmentation is caused primarily by an attack of free radicals.
低密度脂蛋白(LDL)的氧化修饰被认为是动脉粥样硬化的一个重要早期事件,但目前尚未完全明确。为了阐明载脂蛋白B - 100(apoB)的修饰机制,研究了两种具有不同功能的抗氧化剂依布硒啉和普罗布考对铜或水溶性自由基引发剂2,2'-偶氮二(2 - 脒基丙烷)二盐酸盐(AAPH)诱导的LDL氧化修饰的预防作用。依布硒啉通过还原LDL中的氢过氧化物完全抑制了铜诱导的氧化,因为铜依赖性氧化的引发需要LDL中存在微量的氢过氧化物。另一方面,依布硒啉并未抑制AAPH诱导的LDL氧化,AAPH通过热分解产生自由基。在没有依布硒啉的情况下,AAPH诱导的LDL氧化主要产生磷脂酰胆碱氢过氧化物和胆固醇酯氢过氧化物,而在有依布硒啉存在时,氢过氧化物被还原为相应的醇。有趣的是,依布硒啉对AAPH诱导的氧化中完整apoB的相对电泳迁移率增加和片段化影响很小。普罗布考有效抑制了铜或AAPH诱导的LDL脂质氧化,但即使在有普罗布考存在的情况下也观察到了蛋白质修饰。研究表明:(1)脂质氢过氧化物在apoB的修饰(如负电荷增加和片段化)中不起重要作用;(2)自由基对apoB的直接攻击及其被氢过氧化物衍生的脂质氧化产物修饰会增加apoB的负电荷;(3)其片段化主要是由自由基的攻击引起的。