Pryor W A, Squadrito G L
Biodynamics Institute, Louisiana State University, Baton Rouge 70803, USA.
Am J Physiol. 1995 May;268(5 Pt 1):L699-722. doi: 10.1152/ajplung.1995.268.5.L699.
Nitric oxide and superoxide, which are produced by several cell types, rapidly combine to form peroxynitrite. This reaction can result in nitric oxide scavenging, and thus mitigation of the biological effects of superoxide. Also, superoxide can trap and hence modulate the effects of nitric oxide; superoxide dismutase, by controlling superoxide levels, therefore can influence the reaction pathways open to nitric oxide. The production of peroxynitrite, however, causes its own sequelae of events: Although neither .NO nor superoxide is a strong oxidant, peroxynitrite is a potent and versatile oxidant that can attack a wide range of biological targets. The peroxynitrite anion is relatively stable, but its acid, peroxynitrous acid (HOONO), rearranges to form nitrate with a half-life of approximately 1 s at pH 7, 37 degrees C. HOONO exists as a Boltzmann distribution of rotamers; at 5-37 degrees C HOONO has an apparent acidity constant, pKa,app, of 6.8. Oxidation reactions of HOONO can involve two-electron processes (such as an SN2 displacement) or a one-electron transfer (ET) reaction in which the substrate is oxidized by one electron and peroxynitrite is reduced. These oxidation reactions could involve one of two mechanisms. The first mechanism is homolysis of HOONO to give HO. and .NO2, which initially are held together in a solvent cage. This caged pair of radicals (the "geminate" pair) can either diffuse apart, giving free radicals that can perform oxidations, or react together either to form nitrate or to reform HOONO (a process called cage return). A large amount of cage return can explain the small entropy of activation (Arrhenius A-factor) observed for the decomposition of HOONO. A cage mechanism also can explain the residual yield of nitrate that appears to be formed even in the presence of high concentrations of all of the scavengers studied to date, since scavengers capture only free HO. and .NO2 and not caged radicals. If the cage mechanism is correct, the rate of disappearance of peroxynitrite be slower in solvents of higher viscosity, and we do not find this to be the case. The second mechanism is that an activated isomer of peroxynitrous acid, HOONO*, can be formed in a steady state. The HOONO* mechanism can explain the inability of hydroxyl radical scavengers to completely block either nitrate formation or the oxidation of substrates such as methionine, since HOONO* would be less reactive, and therefore more selective, than the hydroxyl radical itself.(ABSTRACT TRUNCATED AT 400 WORDS)
一氧化氮和超氧化物由多种细胞类型产生,它们迅速结合形成过氧亚硝酸盐。该反应会导致一氧化氮被清除,从而减轻超氧化物的生物学效应。此外,超氧化物可以捕获并因此调节一氧化氮的作用;超氧化物歧化酶通过控制超氧化物水平,进而能够影响一氧化氮可利用的反应途径。然而,过氧亚硝酸盐的产生会引发其自身一系列后续事件:尽管一氧化氮和超氧化物都不是强氧化剂,但过氧亚硝酸盐却是一种强大且多功能的氧化剂,能够攻击多种生物靶点。过氧亚硝酸根阴离子相对稳定,但其酸过氧亚硝酸(HOONO)在pH 7、37摄氏度时会重排形成硝酸盐,半衰期约为1秒。HOONO以旋转异构体的玻尔兹曼分布形式存在;在5至37摄氏度时,HOONO的表观酸度常数pKa,app为6.8。HOONO的氧化反应可涉及双电子过程(如SN2取代)或单电子转移(ET)反应,其中底物通过单电子被氧化而过氧亚硝酸盐被还原。这些氧化反应可能涉及两种机制中的一种。第一种机制是HOONO发生均裂生成羟基自由基(HO·)和二氧化氮自由基(·NO2),它们最初在溶剂笼中结合在一起。这种笼状自由基对(“孪连”对)既可以扩散分开,产生能够进行氧化反应的自由基,也可以一起反应形成硝酸盐或重新生成HOONO(一个称为笼返的过程)。大量的笼返现象可以解释观察到的HOONO分解时较小的活化熵(阿仑尼乌斯A因子)。笼状机制也可以解释即使在存在迄今为止所研究的所有高浓度清除剂的情况下仍似乎会形成的硝酸盐残余产率,因为清除剂只能捕获游离的HO·和·NO2,而不能捕获笼状自由基。如果笼状机制正确,那么过氧亚硝酸盐在较高粘度溶剂中的消失速率会更慢,但我们并未发现这种情况。第二种机制是过氧亚硝酸可以形成一种处于稳态的活化异构体HOONO*。HOONO机制可以解释羟基自由基清除剂无法完全阻止硝酸盐形成或蛋氨酸等底物氧化的原因,因为HOONO的反应活性较低,因此比羟基自由基本身更具选择性。(摘要截选至400字)