Bicarbonate inhibits N-nitrosation in oxygenated nitric oxide solutions

被引:90
作者
Caulfield, JL
Singh, SP
Wishnok, JS
Deen, WM
Tannenbaum, SR
机构
[1] MIT,DEPT CHEM,CAMBRIDGE,MA 02139
[2] MIT,DIV TOXICOL,CAMBRIDGE,MA 02139
[3] MIT,DEPT CHEM ENGN,CAMBRIDGE,MA 02139
关键词
D O I
10.1074/jbc.271.42.25859
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
N-Nitrosation in oxygenated nitric oxide (NO.) solutions was previously shown to be significantly inhibited by phosphate and chloride presumably by anion scavenging of the nitrosating agent nitrous anhydride, N-2O3 (Lewis, R. S., Tannenbaum, S, R., and Deen, W. M. (1995) J. Am. Chem. Sec. 117, 3933-3939), Here, bicarbonate is shown to exhibit this same inhibitory effect, Rate constants for reaction of morpholine, phosphate, and bicarbonate with N2O3 relative to N2O3 hydrolysis at pH 8.9 were determined to be (3.7 +/- 0.2) x 10(4) M(-1), (4.0 +/- 0.9) x 10(2) M(-1), and (9.3 +/- 1.5) x 10(2) M(-1), respectively, The morpholine and phosphate rate constants at pH 8.9 are similar to those reported at pH 7.4 assuring that these results are relevant to physiological conditions, The rate constant for this previously unrecognized reaction of bicarbonate with N2O3 suggests the strong scavenging ability of bicarbonate; accordingly, bicarbonate may contribute to reducing deleterious effects of N2O3, This is biologically important due to substantial bicarbonate concentrations in vivo, approximately 30 mM. Bicarbonate was previously shown to alter peroxynitrite reactivity; however, carbon dioxide is the probable reactive species, Bicarbonate is therefore potentially important in determining the fate of two reactive species generated from nitric oxide, N2O3 and ONOO-, and may thus act as a regulator of NO.-induced toxicity.
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页码:25859 / 25863
页数:5
相关论文
共 18 条
[1]  
Carola R., 1990, HUMAN ANATOMY PHYSL
[2]   NITRIC-OXIDE INDUCES OXIDATIVE DAMAGE IN ADDITION TO DEAMINATION IN MACROPHAGE DNA [J].
DEROJASWALKER, T ;
TAMIR, S ;
JI, H ;
WISHNOK, JS ;
TANNENBAUM, SR .
CHEMICAL RESEARCH IN TOXICOLOGY, 1995, 8 (03) :473-477
[3]   PEROXYNITRITE-MEDIATED TYROSINE NITRATION CATALYZED BY SUPEROXIDE-DISMUTASE [J].
ISCHIROPOULOS, H ;
ZHU, L ;
CHEN, J ;
TSAI, M ;
MARTIN, JC ;
SMITH, CD ;
BECKMAN, JS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 298 (02) :431-437
[4]  
KEITH WG, 1969, J CHEM SOC, pA90
[5]   KINETIC-ANALYSIS OF THE FATE OF NITRIC-OXIDE SYNTHESIZED BY MACROPHAGES IN-VITRO [J].
LEWIS, RS ;
TAMIR, S ;
TANNENBAUM, SR ;
DEEN, WM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) :29350-29355
[6]   KINETICS OF THE REACTION OF NITRIC-OXIDE WITH OXYGEN IN AQUEOUS-SOLUTIONS [J].
LEWIS, RS ;
DEEN, WM .
CHEMICAL RESEARCH IN TOXICOLOGY, 1994, 7 (04) :568-574
[7]   KINETICS OF N-NITROSATION IN OXYGENATED NITRIC-OXIDE SOLUTIONS AT PHYSIOLOGICAL PH - ROLE OF NITROUS ANHYDRIDE AND EFFECTS OF PHOSPHATE AND CHLORIDE [J].
LEWIS, RS ;
TANNENBAUM, SR ;
DEEN, WM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (14) :3933-3939
[8]   RAPID REACTION BETWEEN PEROXONITRITE ION AND CARBON-DIOXIDE - IMPLICATIONS FOR BIOLOGICAL-ACTIVITY [J].
LYMAR, SV ;
HURST, JK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (34) :8867-8868
[9]   Mechanism of carbon dioxide-catalyzed oxidation of tyrosine by peroxynitrite [J].
Lymar, SV ;
Jiang, Q ;
Hurst, JK .
BIOCHEMISTRY, 1996, 35 (24) :7855-7861
[10]   CARBONATE ANIONS - EFFECTS ON THE OXIDATION OF LUMINOL, OXIDATIVE HEMOLYSIS, GAMMA-IRRADIATION AND THE REACTION OF ACTIVATED OXYGEN SPECIES WITH ENZYMES CONTAINING VARIOUS ACTIVE-CENTERS [J].
MICHELSON, AM ;
MARAL, J .
BIOCHIMIE, 1983, 65 (02) :95-104