Pennington S N, Smith C P
Lipids. 1978 Oct;13(10):636-43. doi: 10.1007/BF02533738.
Peroxidation of endogenous lipid by liver microsomes, coupled with oxidation of reduced nicotinamide adenine dinucleotide phosphate (NADPH) and measured as thiobarbituric acid reactive materials, is markedly stimulated in the presence of indomethacin [1-(p-chlorobenzyl)-5-methoxy-2-methyl-3-indole acetic acid] (0.1--1.0 mM). Concurrently, indomethacin enhances the lipolysis of membrane phospholipid containing arachidonic acid but has no effect on the rate of O2 uptake in these samples. The system generates a rapidly developed chemiliminescense (CL), the intensity and rate of development of which are related to indomethacin concentration. The microsomal CL generated in the presence of indomethacin is distinct from the previously reported CL in that the time required for maximum intensity development is a matter of seconds (20--180) rather than hours. The enhanced CL is believed to be due to an energy transfer reaction whereby a high energy species transfers energy to the indomethacin molecule, which, in turn, decays via chemiluminescense. An enhanced chemiluminescense was also observed when indomethacin was added to a lipoxidase system and superoxide generating system (axanthine oxidase). Based on inhibitor studies, the rapidly developed chemiluminescense of the microsomal system requires cytochrome P-450 in addition to NADPH and coordinated iron ions. The results indicate that the CL is related to neither hydroxyl free radical nor superoxide anion formation.
在消炎痛[1-(对氯苄基)-5-甲氧基-2-甲基-3-吲哚乙酸](0.1 - 1.0 mM)存在的情况下,肝微粒体对内源性脂质的过氧化作用,与还原型烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的氧化作用相耦合,并以硫代巴比妥酸反应性物质来衡量,会受到显著刺激。同时,消炎痛会增强含花生四烯酸的膜磷脂的脂解作用,但对这些样品中的氧气摄取速率没有影响。该系统会产生快速发展的化学发光(CL),其强度和发展速率与消炎痛浓度相关。在消炎痛存在下产生的微粒体CL与先前报道的CL不同,因为达到最大强度所需的时间是几秒(20 - 180)而不是几小时。增强的CL被认为是由于能量转移反应,即一种高能物质将能量转移到消炎痛分子上,然后消炎痛分子通过化学发光衰变。当消炎痛添加到脂氧化酶系统和超氧化物生成系统(黄嘌呤氧化酶)中时,也观察到化学发光增强。基于抑制剂研究,微粒体系统快速发展的化学发光除了需要NADPH和配位铁离子外,还需要细胞色素P - 450。结果表明,CL既与羟基自由基的形成无关,也与超氧阴离子的形成无关。