A novel reaction mechanism for the formation of S-nitrosothiol in vivo

被引:252
作者
Gow, AJ
Buerk, DG
Ischiropoulos, H
机构
[1] UNIV PENN,INST ENVIRONM MED,SCH MED,PHILADELPHIA,PA 19104
[2] UNIV PENN,DEPT PHYSIOL & BIOENGN,SCH MED,PHILADELPHIA,PA 19104
[3] UNIV PENN,DEPT BIOCHEM BIOPHYS,SCH MED,PHILADELPHIA,PA 19104
关键词
D O I
10.1074/jbc.272.5.2841
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 objective of this study was to investigate the mechanism of S-nitrosothiol formation under physiological conditions. A mechanism is proposed by which nitric oxide ((NO)-N-.) reacts directly with reduced thiol to produce a radical intermediate, R-S-N-.-O-H. This intermediate reduces an electron acceptor to produce S-nitrosothiol. Under aerobic conditions O-2 acts as the electron acceptor and is reduced to produce superoxide (O-2(radical anion)). The following experimental evidence is provided in support of this mechanism. Cysteine accelerates the consumption of (NO)-N-. by 2.5-fold under physiological conditions. The consumption of O-2 in the presence of (NO)-N-. and cysteine is increased by 2.4-fold. The reaction orders of (NO)-N-. and cysteine are second and first order, respectively. The second order of reaction for (NO)-N-. may result from interaction between (NO)-N-. and O-2(radical anion) to form peroxynitrite. In the presence of Cu,Zn-superoxide dismutase, the reaction of (NO)-N-. with cysteine generates hydrogen peroxide, indicating that the reaction generates O-2(radical anion). Finally, the formation of S-nitrosothiol is demonstrated in an anaerobic environment and, as predicted by the mechanism, is dependent on the presence of an electron acceptor. These results demonstrate that under physiological conditions (NO)-N-. reacts directly with thiols to form S-nitrosothiol in the presence of an electron acceptor.
引用
收藏
页码:2841 / 2845
页数:5
相关论文
共 26 条
[1]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[2]   S-NITROSATION OF SERUM-ALBUMIN BY DINITROSYL-IRON COMPLEX [J].
BOESE, M ;
MORDVINTCEV, PI ;
VANIN, AF ;
BUSSE, R ;
MULSCH, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) :29244-29249
[3]  
BUERK DG, 1993, BIOSNESORS THEORY AP, P95
[4]   REACTION OF NITRIC-OXIDE WITH THE FREE SULFHYDRYL-GROUP OF HUMAN SERUM-ALBUMIN YIELDS A SULFENIC ACID AND NITROUS-OXIDE [J].
DEMASTER, EG ;
QUAST, BJ ;
REDFERN, B ;
NAGASAWA, HT .
BIOCHEMISTRY, 1995, 34 (36) :11494-11499
[5]   ACTIVATION OF CORONARY ARTERIAL GUANYLATE-CYCLASE BY NITRIC-OXIDE, NITROPRUSSIDE, AND NITROSOGUANIDINE - INHIBITION BY CALCIUM, LANTHANUM, AND OTHER CATIONS, ENHANCEMENT BY THIOLS [J].
GRUETTER, DY ;
GRUETTER, CA ;
BARRY, BK ;
BARICOS, WH ;
HYMAN, AL ;
KADOWITZ, PJ ;
IGNARRO, LJ .
BIOCHEMICAL PHARMACOLOGY, 1980, 29 (21) :2943-2950
[6]   The role of glutathione in the transport and catabolism of nitric oxide [J].
Hogg, N ;
Singh, RJ ;
Kalyanaraman, B .
FEBS LETTERS, 1996, 382 (03) :223-228
[7]   REQUIREMENT OF THIOLS FOR ACTIVATION OF CORONARY ARTERIAL GUANYLATE-CYCLASE BY GLYCERYL TRINITRATE AND SODIUM-NITRITE - POSSIBLE INVOLVEMENT OF S-NITROSOTHIOLS [J].
IGNARRO, LJ ;
GRUETTER, CA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 631 (02) :221-231
[8]   Reactions of nitric oxide and peroxynitrite with organic molecules and ferrihorseradish peroxidase: Interference with the determination of hydrogen peroxide [J].
Ischiropoulos, H ;
Nelson, J ;
Duran, D ;
AlMehdi, A .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (03) :373-381
[9]   S-nitrosohaemoglobin: A dynamic activity of blood involved in vascular control [J].
Jia, L ;
Bonaventura, C ;
Bonaventura, J ;
Stamler, JS .
NATURE, 1996, 380 (6571) :221-226
[10]   CONTROL OF CORONARY VASCULAR TONE BY NITRIC-OXIDE [J].
KELM, M ;
SCHRADER, J .
CIRCULATION RESEARCH, 1990, 66 (06) :1561-1575