Interactions between nitric oxide and lipid oxidation pathways - Implications for vascular disease

被引:204
作者
O'Donnell, VB
Freeman, BA [1 ]
机构
[1] Univ Alabama Birmingham, Dept Anesthesiol, 946 Tinsley Harrison Tower,619 S 19th St, Birmingham, AL 35233 USA
[2] Univ Alabama Birmingham, Dept Biochem, Birmingham, AL 35233 USA
[3] Univ Alabama Birmingham, Dept Mol Genet, Birmingham, AL 35233 USA
[4] Univ Alabama Birmingham, Ctr Free Rad Biol, Birmingham, AL 35233 USA
[5] Cardiff Univ, Wales heart Res Inst, Cardiff CF4 4XN, S Glam, Wales
关键词
eicosanoid signaling; lipid; nitric oxide; oxygen; free radical;
D O I
10.1161/01.RES.88.1.12
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nitric oxide ((NO)-N-.) signaling pathways and lipid oxidation reactions are of central importance in both the maintenance of vascular homeostasis and the progression of vascular disease. Because both of these pathways involve free radical species that can also react together at extremely fast rates, convergent interactions between these pathways are expected. Biochemical and cell biology studies have defined multiple interactions of (NO)-N-. with oxidizing lipids that could lead to either vascular protection or potentiation of inflammatory vascular injury. For example, low levels of (NO)-N-. generated by endothelial nitric oxide synthase can terminate propagating lipid radicals and inhibit lipoxygenases, reactions that would be protective, Alternatively, if generated at elevated levels, for example, after inducible nitric oxide synthase expression in inflammation, (NO)-N-. can be converted to prooxidant species, such as peroxynitrite (ONOO-) and nitrogen dioxide ((NO2)-N-.), that can potentiate inflammatory injury to vascular cells, Finally, both enzymatic and nonenzymatic lipid oxidation reactions can influence (NO)-N-. bioactivity by directly scavenging (NO)-N-. or altering the induction and catalytic activity of nitric oxide synthase enzymes. In this review, we summarize the biochemical interactions between (NO)-N-. and lipid oxidation reactions and discuss the recognized and potential roles of these reactions in the vasculature.
引用
收藏
页码:12 / 21
页数:10
相关论文
共 152 条
[111]   Downregulation of soluble guanylyl cyclase in young and aging spontaneously hypertensive rats [J].
Ruetten, H ;
Zabel, U ;
Linz, W ;
Schmidt, HHHW .
CIRCULATION RESEARCH, 1999, 85 (06) :534-541
[112]   NATURE OF THE NITRIC-OXIDE COMPLEXES OF LIPOXYGENASE [J].
SALERNO, JC ;
SIEDOW, JN .
BIOCHIMICA ET BIOPHYSICA ACTA, 1979, 579 (01) :246-251
[113]   Nitric oxide-mediated cyclooxygenase activation - A key event in the antiplatelet effects of nitrovasodilators [J].
Salvemini, D ;
Currie, MG ;
Mollace, V .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (11) :2562-2568
[114]   NITRIC-OXIDE ACTIVATES CYCLOOXYGENASE ENZYMES [J].
SALVEMINI, D ;
MISKO, TP ;
MASFERRER, JL ;
SEIBERT, K ;
CURRIE, MG ;
NEEDLEMAN, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (15) :7240-7244
[115]   INVIVO CYCLOOXYGENASE EXPRESSION IN SYNOVIAL TISSUES OF PATIENTS WITH RHEUMATOID-ARTHRITIS AND OSTEOARTHRITIS AND RATS WITH ADJUVANT AND STREPTOCOCCAL CELL-WALL ARTHRITIS [J].
SANO, H ;
HLA, T ;
MAIER, JAM ;
CROFFORD, LJ ;
CASE, JP ;
MACIAG, T ;
WILDER, RL .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (01) :97-108
[116]  
Sasaki M, 1997, AM J HYPERTENS, V10, P371
[117]   Normalization of blood pressure and renal vascular resistance in SHR with a membrane-permeable superoxide dismutase mimetic - Role of nitric oxide [J].
Schnackenberg, CG ;
Welch, WJ ;
Wilcox, CS .
HYPERTENSION, 1998, 32 (01) :59-64
[118]   Two-week administration of tempol attenuates both hypertension and renal excretion of 8-iso prostaglandin F2α [J].
Schnackenberg, CG ;
Wilcox, CS .
HYPERTENSION, 1999, 33 (01) :424-428
[119]   Attenuation of diet-induced atherosclerosis in rabbits with a highly selective 15-lipoxygenase inhibitor lacking significant antioxidant properties [J].
Sendobry, SM ;
Cornicelli, JA ;
Welch, K ;
Bocan, T ;
Tait, B ;
Trivedi, BK ;
Colbry, N ;
Dyer, RD ;
Feinmark, SJ ;
Daugherty, A .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 120 (07) :1199-1206
[120]   Macrophage-mediated 15-lipoxygenase expression protects against atherosclerosis development [J].
Shen, JH ;
Herderick, E ;
Cornhill, JF ;
Zsigmond, E ;
Kim, HS ;
Kuhn, H ;
Guevara, NV ;
Chan, L .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (10) :2201-2208