Recent advances in the understanding of the role of nitric oxide in cardiovascular homeostasis

被引:137
作者
Schulz, R
Rassaf, T
Massion, PB
Kelm, M
Balligand, JL
机构
[1] Univ Klinikum Essen, Zentrum Innere Med, Inst Pathophysiol, Essen, Germany
[2] Univ Dusseldorf, Klin Kardiol Pulmol Angiol, D-40225 Dusseldorf, Germany
[3] Catholic Univ Louvain, Unit Pharmacol & Therapeut, B-1200 Brussels, Belgium
关键词
D O I
10.1016/j.pharmthera.2005.04.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nitric oxide synthases (NOS) are the enzymes responsible for nitric oxide (NO) generation. To date, 3 distinct NOS isoforms have been identified: neuronal NOS (NOS1), inducible NOS (NOS2), and endothelial NOS (NOS3). Biochemically, NOS consists of a flavin-containing reductase domain, a heme-containing oxygenase domain, and regulatory sites. NOS catalyse an overall 5-electron oxidation of one N-omega-atorn of the guanidino group Of L-arginine to form NO and L-Citrulline. NO exerts a plethora of biological effects in the cardiovascular system. The basal formation of NO in mitochondria by a mitochondrial NOS seems to be one of the main regulators of cellular respiration, mitochondrial transmembrane potential, and transmembrane proton gradient. This review focuses on recent advances in the understanding of the role of enzyme and enzyme-independent NO formation, regulation of NO bioactivity, new aspects of NO on cardiac function and morphology, and the clinical impact and perspectives of these recent advances in our knowledge on NO-related pathways. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:225 / 256
页数:32
相关论文
共 431 条
[61]   Alterations of gene expression in failing myocardium following left ventricular assist device support [J].
Chen, YJ ;
Park, S ;
Li, YF ;
Missov, E ;
Hou, MX ;
Han, XQ ;
Hall, JL ;
Miller, LW ;
Bache, RJ .
PHYSIOLOGICAL GENOMICS, 2003, 14 (03) :251-260
[62]   Nitric oxide modulates myocardial oxygen consumption in the failing heart [J].
Chen, YJ ;
Traverse, JH ;
Du, RS ;
Hou, MX ;
Bache, RJ .
CIRCULATION, 2002, 106 (02) :273-279
[63]   AMP-activated protein kinase phosphorylation of endothelial NO synthase [J].
Chen, ZP ;
Mitchelhill, KI ;
Michell, BJ ;
Stapleton, D ;
Rodriguez-Crespo, I ;
Witters, LA ;
Power, DA ;
de Montellano, PRO ;
Kemp, BE .
FEBS LETTERS, 1999, 443 (03) :285-289
[64]   Aldosterone inhibits inducible nitric oxide synthase in neonatal rat cardiomyocytes [J].
Chun, TY ;
Bloem, LJ ;
Pratt, JH .
ENDOCRINOLOGY, 2003, 144 (05) :1712-1717
[65]   Persistent inhibition of cell respiration by nitric oxide:: Crucial role of S-nitrosylation of mitochondrial complex I and protective action of glutathione [J].
Clementi, E ;
Brown, GC ;
Feelisch, M ;
Moncada, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (13) :7631-7636
[66]   Asymmetrical dimethylarginine - The Uber marker? [J].
Cooke, JP .
CIRCULATION, 2004, 109 (15) :1813-1818
[67]   Nitrite reduction to nitric oxide by deoxyhemoglobin vasodilates the human circulation [J].
Cosby, K ;
Partovi, KS ;
Crawford, JH ;
Patel, RP ;
Reiter, CD ;
Martyr, S ;
Yang, BK ;
Waclawiw, MA ;
Zalos, G ;
Xu, XL ;
Huang, KT ;
Shields, H ;
Kim-Shapiro, DB ;
Schechter, AN ;
Cannon, RO ;
Gladwin, MT .
NATURE MEDICINE, 2003, 9 (12) :1498-1505
[68]   TETRAHYDROBIOPTERIN AND DYSFUNCTION OF ENDOTHELIAL NITRIC-OXIDE SYNTHASE IN CORONARY-ARTERIES [J].
COSENTINO, F ;
KATUSIC, ZS .
CIRCULATION, 1995, 91 (01) :139-144
[69]   High glucose causes upregulation of cyclooxygenase-2 and alters prostanoid profile in human endothelial cells -: Role of protein kinase C and reactive oxygen species [J].
Cosentino, F ;
Eto, M ;
De Paolis, P ;
van der Loo, B ;
Bachschmid, M ;
Ullrich, V ;
Kouroedov, A ;
Gatti, CD ;
Joch, H ;
Volpe, M ;
Lüscher, TF .
CIRCULATION, 2003, 107 (07) :1017-1023
[70]   Classic preconditioning decreases the harmful accumulation of nitric oxide during ischemia and reperfusion in rat hearts [J].
Csonka, C ;
Szilvássy, Z ;
Fülöp, F ;
Páli, T ;
Blasig, IE ;
Tosaki, A ;
Schulz, R ;
Ferdinandy, P .
CIRCULATION, 1999, 100 (22) :2260-2266