Peroxynitrite: biochemistry, pathophysiology and development of therapeutics

被引:1636
作者
Szabo, Csaba
Ischiropoulos, Harry
Radi, Rafael
机构
[1] Univ Med & Dent New Jersey, Dept Surg, Newark, NJ 07103 USA
[2] Semmelweis Univ, Sch Med, CellScreen Appl Res Ctr, H-1085 Budapest, Hungary
[3] Childrens Hosp Philadelphia, Stokes Res Inst, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Dept Pharmacol, Philadelphia, PA 19104 USA
[5] Univ Penn, Philadelphia, PA 19104 USA
[6] Univ Republica, Fac Med, Dept Biochem, Montevideo 11800, Uruguay
[7] Univ Republica, Fac Med, Ctr Free Rad & Biomed Res, Montevideo 11800, Uruguay
关键词
D O I
10.1038/nrd2222
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Peroxynitrite - the product of the diffusion-controlled reaction of nitric oxide with superoxide radical - is a short-lived oxidant species that is a potent inducer of cell death. Conditions in which the reaction products of peroxynitrite have been detected and in which pharmacological inhibition of its formation or its decomposition have been shown to be of benefit include vascular diseases, ischaemia - reperfusion injury, circulatory shock, inflammation, pain and neurodegeneration. In this Review, we first discuss the biochemistry and pathophysiology of peroxynitrite and then focus on pharmacological strategies to attenuate the toxic effects of peroxynitrite. These include its catalytic reduction to nitrite and its isomerization to nitrate by metalloporphyrins, which have led to potential candidates for drug development for cardiovascular, inflammatory and neurodegenerative diseases.
引用
收藏
页码:662 / 680
页数:19
相关论文
共 312 条
[31]  
Boczkowski J, 2001, BIOL SIGNAL RECEPT, V10, P66
[32]  
BOLANOS JP, 1995, J NEUROCHEM, V64, P1965
[33]   The mechanism by which 4-hydroxy-2,2,6,6-tetramethylpiperidene-1-oxyl (tempol) diverts peroxynitrite decomposition from nitrating to nitrosating species [J].
Bonini, MG ;
Mason, RP ;
Augusto, O .
CHEMICAL RESEARCH IN TOXICOLOGY, 2002, 15 (04) :506-511
[34]   Carbon dioxide stimulates the production of thiyl, sulfinyl, and disulfide radical anion from thiol oxidation by peroxynitrite [J].
Bonini, MG ;
Augusto, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :9749-9754
[35]   Release of cytochrome c from heart mitochondria is induced by high Ca2+ and peroxynitrite and is responsible for Ca2+-induced inhibition of substrate oxidation [J].
Borutaite, V ;
Morkuniene, R ;
Brown, GC .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1999, 1453 (01) :41-48
[36]   Reactivity of peroxynitrite and nitric oxide with LDL [J].
Botti, H ;
Trostchansky, A ;
Batthyány, C ;
Rubbo, H .
IUBMB LIFE, 2005, 57 (06) :407-412
[37]   Preservation of human islet cell functional mass by anti-oxidative action of a novel SOD mimic compound [J].
Bottino, R ;
Balamurugan, AN ;
Bertera, S ;
Pietropaolo, M ;
Trucco, M ;
Piganelli, JD .
DIABETES, 2002, 51 (08) :2561-2567
[38]   A catalytic antioxidant (AEOL 10150) attenuates expression of inflammatory genes in stroke [J].
Bowler, RP ;
Sheng, HX ;
Enghild, JJ ;
Pearlstein, RD ;
Warner, DS ;
Crapo, JD .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (08) :1141-1152
[39]   Attenuation of oxidation and nitration reactions of peroxynitrite by selenomethionine, selenocystine and ebselen [J].
Briviba, K ;
Roussyn, I ;
Sharov, VS ;
Sies, H .
BIOCHEMICAL JOURNAL, 1996, 319 :13-15
[40]   Inhibition of mitochondrial respiratory complex I by nitric oxide, peroxynitrite and S-nitrosothiols [J].
Brown, GC ;
Borutaite, V .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2004, 1658 (1-2) :44-49