Effect of •NO on the decomposition of peroxynitrite:: Reaction of N2O3 with ONOO-

被引:62
作者
Goldstein, S [1 ]
Czapski, G
Lind, J
Merényi, G
机构
[1] Hebrew Univ Jerusalem, Dept Phys Chem, IL-91904 Jerusalem, Israel
[2] Royal Inst Technol, Dept Chem Nucl Chem, S-10044 Stockholm 70, Sweden
关键词
D O I
10.1021/tx9802522
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Nitric oxide reacts slowly with ONOO- (k < 1.3 x 10(-3) M-1 s(-1)), and therefore does not affect the stability of peroxynitrite at pH >12. A chain consumption of peroxynitrite by (NO)-N-. takes place at pH<12 through the reaction of N2O3 with ONOO-, where the former is formed through two initiation steps: (i) autoxidation of (NO)-N-., which is the main process in alkaline solutions, and (ii) spontaneous decomposition of peroxynitrite. The effect of (NO)-N-. on the decomposition of peroxynitrite depends on the rate of the reaction of ONOO- with N2O3 (propagation step) relative to that of the hydrolysis of N2O3 (termination step). Therefore, rapid consumption of peroxynitrite occurs upon increasing the peroxynitrite concentration, decreasing the phosphate concentration, and lowering the pH, as the hydrolysis of N2O3 is base-catalyzed. The rate constant of the reaction of ONOO- with N2O3 has been determined in alkaline solutions to be (3.1 +/- 9.3) x 10(8) M-1 s(-1). The decomposition of ONOOH in acidic solutions is hardly affected by (NO)-N-., as N2O3 does not react with ONOOH. Under physiological conditions, the reaction of (NO)-N-. with peroxynitrite cannot give rise to a chain consumption of peroxynitrite as the reaction of N2O3 with the relatively low concentrations of peroxynitrite cannot compete with the hydrolysis of N2O3.
引用
收藏
页码:132 / 136
页数:5
相关论文
共 21 条
[1]   AUTOXIDATION OF NO IN AQUEOUS-SOLUTION [J].
AWAD, HH ;
STANBURY, DM .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1993, 25 (05) :375-381
[2]   Bicarbonate inhibits N-nitrosation in oxygenated nitric oxide solutions [J].
Caulfield, JL ;
Singh, SP ;
Wishnok, JS ;
Deen, WM ;
Tannenbaum, SR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (42) :25859-25863
[3]   KINETICS OF NITRIC-OXIDE AUTOXIDATION IN AQUEOUS-SOLUTION IN THE ABSENCE AND PRESENCE OF VARIOUS REDUCTANTS - THE NATURE OF THE OXIDIZING INTERMEDIATES [J].
GOLDSTEIN, S ;
CZAPSKI, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (49) :12078-12084
[4]   Direct and indirect oxidations by peroxynitrite, neither involving the hydroxyl radical [J].
Goldstein, S ;
Squadrito, GL ;
Pryor, WA ;
Czapski, G .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 21 (07) :965-974
[5]   Oxidation of peroxynitrite by inorganic radicals: A pulse radiolysis study [J].
Goldstein, S ;
Saha, A ;
Lymar, SV ;
Czapski, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (22) :5549-5554
[6]   Mechanism of the nitrosation of thiols and amines by oxygenated center dot NO solutions: The nature of the nitrosating intermediates [J].
Goldstein, S ;
Czapski, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (14) :3419-3425
[7]   Formation of peroxynitrite from the nitrosation of hydrogen peroxide by an oxygenated nitric oxide solution [J].
Goldstein, S ;
Czapski, G .
INORGANIC CHEMISTRY, 1996, 35 (20) :5935-5940
[8]  
GOLSTEIN S, 1998, J AM CHEM SOC, V120, P3458
[9]  
Graetzel M., 1970, BER BUNSEN PHYS CHEM, V74, P488
[10]   CHEMISTRY OF PERNITRITES .I. KINETICS OF DECOMPOSITION OF PERNITROUS ACID [J].
HUGHES, MN ;
NICKLIN, HG .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1968, (02) :450-&