Product formation and kinetic simulations in the pH range 1-14 account for a free-radical mechanism of peroxynitrite decomposition

被引:64
作者
Kirsch, M
Korth, HG
Wensing, A
Sustmann, R
de Groot, H
机构
[1] Univ Klinikum Essen, Inst Physiol Chem, D-45122 Essen, Germany
[2] Univ Duisburg Essen, Inst Organ Chem, D-45117 Essen, Germany
关键词
peroxynitrite; hydroxyl radical; oxygen; kinetics; principal component analysis; oxygen formation;
D O I
10.1016/j.abb.2003.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The yields of nitrate and nitrite from decomposition of peroxynitrite in phosphate buffer at 37degreesC were determined in the pH range 1-14. The NO2-/NO3- yields showed a stepwise variation with pH, with inflection points at approximately pH 3.1, 5.8, 6.8, 8.0, and 11.9. Nitrite formation increased strongly above pH 7 at the expense of nitrate, but above pH 12 nitrate again became the major product (80% at pH 14). At this pH, the Arrhenius parameters were E-a = 24.1 +/- 0.2 kcal mol(-1) and A = (4.9 +/- 1.3) x 10(12) s(-1). The yields of NO2-, NO3-, and O-2 measured at pH 5.8, 7.4, and 8.5 as a function of the initial peroxynitrite concentration (50-1000 muM) were linear only at pH 5.8. In the presence of carbon dioxide, oxygen production at pH 7.5 and pH 10 was found to be linear on the CO, concentration. The experimental observations were satisfactorily reproduced by kinetic simulations including principal component analyses, These data strongly suggest that the chemistry of peroxynitrite is exclusively mediated by (NO2)-N-. and HO. radicals in the absence, and by (NO2)-N-. and CO3.- radicals in the presence of CO2. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:133 / 150
页数:18
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