Oxidized LDLs affect nitric oxide and radical generation in brain endothelial cells

被引:12
作者
Hamdheydari, L
Christov, A
Ottman, T
Hensley, K
Grammas, P [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73190 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Ctr Neurosci, Oklahoma City, OK USA
[3] Oklahoma Med Res Fdn, Free Rad Biol & Aging, Oklahoma City, OK 73104 USA
关键词
microvessels; oxidative stress; oxidized lipids; nitric oxide; membrane fluidity; reactive oxygen species;
D O I
10.1016/j.bbrc.2003.10.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
There is an increase in the generation of reactive oxygen species and nitric oxide in the cerebral microcirculation in Alzheimer's disease. The factors that cause this increase in oxidative stress have not been identified. Increasing evidence suggests that there are common mechanisms in atherosclerosis and Alzheimer's disease. The objective of this study was to determine the effects of oxidized low density lipoproteins (LDLs) on brain endothelial cells. Cultured rat brain endothelial cells were treated with either native LDL (10mug/ml) or LDL oxidized in vitro using 4-hydroxy-2-nonenal (HNE-LDL) (10mug/ml), for 24h. The results showed that HNE-LDL significantly increased production of nitric oxide (p < 0.01), decreased membrane fluidity (p < 0.05), and increased reactive oxygen species generation (p < 0.01). These data demonstrate that oxidized LDLs affect nitric oxide and radical generation in brain endothelial cells and could contribute to cerebrovascular dysfunction in Alzheimer's disease. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:486 / 490
页数:5
相关论文
共 45 条
[1]
Protein oxidation in the brain in Alzheimer's disease [J].
Aksenov, MY ;
Aksenova, MV ;
Butterfield, DA ;
Geddes, JW ;
Markesbery, WR .
NEUROSCIENCE, 2001, 103 (02) :373-383
[3]
Aliev G, 2002, BRAIN PATHOL, V12, P21
[4]
Atherosclerotic lesions are associated with increased immunoreactivity for inducible nitric oxide synthase and endothelin-1 in thoracic aortic intimal cells of hyperlipidemic Watanabe rabbits [J].
Aliev, G ;
Smith, MA ;
Turmaine, M ;
Neal, ML ;
Zimina, TV ;
Friedland, RP ;
Perry, G ;
LaManna, JC ;
Burnstock, G .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2001, 71 (01) :40-54
[5]
MEASUREMENT OF NITRIC-OXIDE IN BIOLOGICAL MODELS [J].
ARCHER, S .
FASEB JOURNAL, 1993, 7 (02) :349-360
[6]
Rate sensitivity of shear-induced changes in the lateral diffusion of endothelial cell membrane lipids: a role for membrane perturbation in shear-induced MAPK activation [J].
Butler, PJ ;
Tsou, TC ;
Li, JYS ;
Usami, S ;
Chien, S .
FASEB JOURNAL, 2001, 15 (14) :216-+
[7]
Lipid peroxidation and protein oxidation in Alzheimer's disease brain:: Potential causes and consequences involving amyloid β-peptide-associated free radical oxidative stress [J].
Butterfield, DA ;
Lauderback, CM .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (11) :1050-1060
[8]
Low density lipoprotein oxidation, antioxidants, and atherosclerosis [J].
Catapano, AL ;
Maggi, FM ;
Tragni, E .
CURRENT OPINION IN CARDIOLOGY, 2000, 15 (05) :355-363
[9]
LOX-1, the receptor for oxidized low-density lipoprotein identified from endothelial cells: implications in endothelial dysfunction and atherosclerosis [J].
Chen, MJ ;
Masaki, T ;
Sawamura, T .
PHARMACOLOGY & THERAPEUTICS, 2002, 95 (01) :89-100
[10]
Christov A., 2003, METHOD PHARMACOL TOX, P175