Kawai Y, Ogamo A, Nakagawa Y
School of Pharmaceutical Sciences, Kitasato University, Minato-ku, Tokyo, 108-8641, Japan.
J Biochem. 1999 Jul;126(1):115-20. doi: 10.1093/oxfordjournals.jbchem.a022411.
The production of phospholipid hydroperoxide and aldehydic phospholipid was examined in human red blood cell (RBC) membranes after peroxidation with 2,2-azobis(2-amidinopropane)dihydrochloride (AAPH) or xanthine/xanthine oxidase (XO/XOD/Fe3+). Both radical-generation systems caused a profound decrease in the amount of polyunsaturated fatty acid (PUFA) in choline glycerophospholipid (CGP) and induced formation of peroxidized CGP in RBC membranes to different extents. No consistent generation of peroxidized lipids from CGP was evident after peroxidation with XO/XOD/Fe3+, which caused the apparent decomposition of phospholipids and the formation of large amounts of thiobarbituric acid-reactive substance (TBARS). On the other hand, CGP hydroperoxide was formed as a primary product of peroxidation with AAPH. Aldehydic CGP was also detected as a secondary product of hydroperoxide decomposition in AAPH-peroxidized RBC membranes. Aldehydic CGP was preferentially generated from arachidonoyl CGP rather than from linoleoyl CGP in AAPH-peroxidized membranes. AAPH mainly oxidized CGP to hydroperoxide and aldehydic phospholipids. The sum of hydroperoxide and aldehyde of CGP corresponded to the loss of CGP due to peroxidation by AAPH. This result indicates that CGP was mainly converted into these two oxidized phospholipids in AAPH-peroxidized RBC membranes.
在用2,2 - 偶氮二(2 - 脒基丙烷)二盐酸盐(AAPH)或黄嘌呤/黄嘌呤氧化酶(XO/XOD/Fe3+)进行过氧化反应后,检测了人红细胞(RBC)膜中磷脂氢过氧化物和醛基磷脂的生成情况。这两种自由基生成系统均导致胆碱甘油磷脂(CGP)中多不饱和脂肪酸(PUFA)含量大幅下降,并在不同程度上诱导RBC膜中过氧化CGP的形成。在用XO/XOD/Fe3+过氧化后,未发现CGP持续生成过氧化脂质,该系统导致磷脂明显分解并形成大量硫代巴比妥酸反应性物质(TBARS)。另一方面,CGP氢过氧化物是AAPH过氧化反应的主要初级产物。在AAPH过氧化的RBC膜中,醛基CGP也被检测为氢过氧化物分解的次级产物。在AAPH过氧化的膜中,醛基CGP优先由花生四烯酰基CGP而非亚油酰基CGP生成。AAPH主要将CGP氧化为氢过氧化物和醛基磷脂。CGP的氢过氧化物和醛的总和与AAPH过氧化导致的CGP损失相对应。这一结果表明,在AAPH过氧化的RBC膜中,CGP主要转化为这两种氧化磷脂。