Rubbo H, Radi R, Trujillo M, Telleri R, Kalyanaraman B, Barnes S, Kirk M, Freeman B A
Department of Anesthesiology, University of Alabama at Birmingham 35233.
J Biol Chem. 1994 Oct 21;269(42):26066-75.
Superoxide (O2-.), nitric oxide (.NO), and their reaction product peroxynitrite (ONOO-) have all been shown to independently exert toxic target molecule reactions. Because these reactive species are often generated in excess during diverse inflammatory and other pathologic circumstances, we assessed the influence of .NO on membrane lipid peroxidation induced by O2-., H2O2, and .OH derived from xanthine oxidase (XO) and by ONOO-. Experimental conditions in lipid oxidation systems were adjusted to yield different rates of delivery of .NO, relative to rates of O2-. and H2O2 generation, by infusion of either .NO or via .NO released from S-nitroso-N-acetylpenicillamine or S-nitrosoglutathione. Peroxidation of phosphatidylcholine liposomes was assessed by formation of thiobarbituric acid-reactive products and by liquid chromatography-mass spectrometry. Liposomes exposed to XO-derived reactive species in the presence of .NO exhibited both stimulation and inhibition of lipid peroxidation, depending on the ratio of the rates of reactive oxygen species production and .NO introduction into reaction systems. Nitric oxide alone did not induce lipid peroxidation. Linolenic acid emulsions peroxidized by XO-derived reactive species showed similar dose-dependent regulation of lipid peroxidation by .NO. Mass spectral analysis of oxidation products showed formation of nitrito-, nitro-, nitrosoperoxo-, and/or nitrated lipid oxidation adducts, demonstrating that .NO serves as a potent terminator of radical chain propagation reactions. Electron spin resonance (ESR) analysis of incubation mixtures provided no evidence for formation of paramagnetic iron-lipid-nitric oxide complexes in reaction systems. Peroxynitrite-dependent lipid peroxidation, which predominantly occurs by metal-independent mechanisms, was also inhibited by .NO. Peroxynitrite-mediated benzoate hydroxylation was partially inhibited by .NO, inferring reaction between .NO and ONOOH. It is concluded that .NO can both stimulate O2-./H2O2/.OH-induced lipid oxidation and mediate oxidant-protective reactions in membranes at higher rates of .NO production, with the prooxidant versus antioxidant outcome critically dependent on relative concentrations of individual reactive species. Prooxidant reactions of .NO will occur after O2-. reaction with .NO to yield potent secondary oxidants such as ONOO- and the antioxidant effects of .NO a consequence of direct reaction with alkoxyl and peroxyl radical intermediates during lipid peroxidation, thus terminating lipid radical chain propagation reactions.
超氧阴离子(O₂⁻·)、一氧化氮(·NO)及其反应产物过氧亚硝酸根(ONOO⁻)均已被证明可独立引发毒性靶分子反应。由于这些活性物质在多种炎症及其他病理情况下常过量生成,我们评估了·NO对由黄嘌呤氧化酶(XO)产生的O₂⁻·、H₂O₂和·OH以及ONOO⁻所诱导的膜脂质过氧化的影响。通过注入·NO或经由S - 亚硝基 - N - 乙酰青霉胺或S - 亚硝基谷胱甘肽释放的·NO,调整脂质氧化系统中的实验条件,以使·NO的递送速率相对于O₂⁻·和H₂O₂的生成速率有所不同。通过硫代巴比妥酸反应产物的形成以及液相色谱 - 质谱法评估磷脂酰胆碱脂质体的过氧化情况。在·NO存在下,暴露于XO衍生的活性物质的脂质体表现出脂质过氧化的刺激和抑制作用,这取决于活性氧生成速率与·NO引入反应系统的速率之比。单独的一氧化氮不会诱导脂质过氧化。由XO衍生的活性物质过氧化的亚麻酸乳液显示出·NO对脂质过氧化的类似剂量依赖性调节。氧化产物的质谱分析表明形成了亚硝基 - 、硝基 - 、亚硝基过氧 - 和/或硝化脂质氧化加合物,表明·NO作为自由基链传播反应的有效终止剂。对孵育混合物的电子自旋共振(ESR)分析未提供反应系统中顺磁性铁 - 脂质 - 一氧化氮复合物形成的证据。主要通过非依赖金属机制发生的过氧亚硝酸根依赖性脂质过氧化也受到·NO的抑制。·NO部分抑制了过氧亚硝酸根介导的苯甲酸羟化反应,推断·NO与ONOOH之间发生了反应。得出的结论是,·NO既能刺激O₂⁻·/H₂O₂/·OH诱导的脂质氧化,又能在·NO生成速率较高时介导膜中的抗氧化反应,促氧化与抗氧化结果关键取决于各个活性物质的相对浓度。·NO的促氧化反应将在O₂⁻·与·NO反应生成诸如ONOO⁻等强效二级氧化剂之后发生,而·NO的抗氧化作用是脂质过氧化过程中与烷氧基和过氧自由基中间体直接反应的结果,从而终止脂质自由基链传播反应。