The inversely proportional relation between nitric oxide and lipid peroxidation in atherosclerotic plaque formation in human

被引:5
作者
Baskin, Y
Baskin, H [1 ]
Guner, G
Tuzun, E
Oto, O
机构
[1] Dokuz Eylul Univ, Sch Med, Dept Microbiol & Clin Microbiol, Izmir, Turkey
[2] Dokuz Eylul Univ, Sch Med, Dept Biochem, Izmir, Turkey
[3] Celal Bayar Univ, Sch Med, Dept Cardiovasc Surg, Manisa, Turkey
[4] Dokuz Eylul Univ, Sch Med, Dept Cardiovasc Surg, Izmir, Turkey
[5] Minist Hlth, Reg Inst Hyg, Izmir, Turkey
关键词
atherosclerosis; nitric oxide; lipid peroxidation;
D O I
10.1016/S0167-5273(02)00596-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is known that in the presence of oxygen radicals, anti-atherogenic nitric oxide is converted into pro-atherogenic products, which increase lipid peroxidation. In this study, plaque-free atherosclerotic tissues (n=26), atherosclerotic plaques (n=26) and fetal tissues (n=2; as control) were evaluated. High nitrite, but low malondialdehyde, levels in non-atherosclerotic tissues may show the protective role of nitric oxide from atherosclerosis. In plaque-developed tissues nitrite levels were three times, and lipid peroxidation levels were 10 times, higher than non-plaque developed tissues. In the atherosclerotic plaque forming process, the role of nitric oxide can be discovered according to the lipid peroxidation of tissues. In conclusion, the results of this study show an inversely proportional relation between pro-and anti-atherogenic effects of nitric oxide in the pathogenesis of atherosclerotic vascular diseases. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:53 / 57
页数:5
相关论文
共 16 条
[1]   Herpes simplex virus type 2 synergizes with interferon-gamma in the induction of nitric oxide production in mouse macrophages through autocrine secretion of tumour necrosis factor-alpha [J].
Baskin, H ;
EllermannEriksen, S ;
Lovmand, J ;
Mogensen, SC .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :195-203
[2]   ATHEROSCLEROSIS - BASIC MECHANISMS - OXIDATION, INFLAMMATION, AND GENETICS [J].
BERLINER, JA ;
NAVAB, M ;
FOGELMAN, AM ;
FRANK, JS ;
DEMER, LL ;
EDWARDS, PA ;
WATSON, AD ;
LUSIS, AJ .
CIRCULATION, 1995, 91 (09) :2488-2496
[3]  
Cannon RO, 1998, CLIN CHEM, V44, P1809
[4]  
DING AH, 1988, J IMMUNOL, V141, P2407
[5]   On the role of vitamin C and other antioxidants in atherogenesis and vascular dysfunction [J].
Frei, B .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 222 (03) :196-204
[6]   Presence of hypochlorite-modified proteins in human atherosclerotic lesions [J].
Hazell, LJ ;
Arnold, L ;
Flowers, D ;
Waeg, G ;
Malle, E ;
Stocker, R .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (06) :1535-1544
[7]   LOW CONCENTRATION OF OXIDIZED LOW-DENSITY-LIPOPROTEIN AND LYSOPHOSPHATIDYLCHOLINE UP-REGULATE CONSTITUTIVE NITRIC-OXIDE SYNTHASE MESSENGER-RNA EXPRESSION IN BOVINE AORTIC ENDOTHELIAL-CELLS [J].
HIRATA, K ;
MIKI, N ;
KURODA, Y ;
SAKODA, T ;
KAWASHIMA, S ;
YOKOYAMA, M .
CIRCULATION RESEARCH, 1995, 76 (06) :958-962
[8]   MEMBRANE LIPID-PEROXIDATION IN ERYTHROCYTES OF THE NEWBORN [J].
JAIN, SK .
CLINICA CHIMICA ACTA, 1986, 161 (03) :301-306
[9]   Reactive nitrogen intermediates promote low density lipoprotein oxidation in human atherosclerotic intima [J].
Leeuwenburgh, C ;
Hardy, MM ;
Hazen, SL ;
Wagner, P ;
Ohishi, S ;
Steinbrecher, UP ;
Heinecke, JW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (03) :1433-1436
[10]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265