The role of natural antioxidants in preserving the biological activity of endothelium-derived nitric oxide

被引:137
作者
Carr, A [1 ]
Frei, B [1 ]
机构
[1] Oregon State Univ, Linus Pauling Inst, Corvallis, OR 97331 USA
关键词
antioxidants; free radical; nitric oxide; thiols; vitamin C; vitamin E;
D O I
10.1016/S0891-5849(00)00225-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endothelium-derived nitric oxide (EDNO) is a pivotal molecule in the regulation of vascular tone via the stimulation of vascular smooth muscle cell relaxation and concomitant vasodilation. In addition, EDNO exerts a number of other potent antiatherogenic effects, including inhibition of leukocyte-endothelial interactions, smooth muscle cell proliferation, and platelet aggregation. Endothelial vasodilator dysfunction has been observed in patients with CAD or coronary risk factors such as hypercholesterolemia, hyperhomocysteinemia, essential hypertension, diabetes mellitus, smoking, and aging. Most of these conditions are associated with increased oxidative stress, particularly increased production of superoxide radicals and elevated levels of oxidized LDL, both of which can attenuate the biological activity of EDNO. The levels of superoxide and oxidized LDL can be decreased by administering the small molecule antioxidants vitamins E and C. Vitamin C also spares intracellular thiols, which in turn can stabilize EDNO through the formation of biologically active S-nitrosothiols. Here we review the role that vitamins E and C and thiol compounds play in endothelium-dependent vasodilation. Understanding the mechanisms of the reversal of endothelial dysfunction by natural antioxidants will lead to successful therapeutic interventions of CAD and its clinical sequelae. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:1806 / 1814
页数:9
相关论文
共 95 条
  • [1] LOW-DENSITY LIPOPROTEINS INHIBIT ENDOTHELIUM-DEPENDENT RELAXATION IN RABBIT AORTA
    ANDREWS, HE
    BRUCKDORFER, KR
    DUNN, RC
    JACOBS, M
    [J]. NATURE, 1987, 327 (6119) : 237 - 239
  • [2] Dietary L-arginine and α-tocopherol reduce vascular oxidative stress and preserve endothelial function in hypercholesterolemic rabbits via different mechanisms
    Böger, RH
    Böde-Boger, SM
    Phivthong-ngam, L
    Brandes, RP
    Schwedhelm, E
    Mügge, A
    Böhme, M
    Tsikas, D
    Frölich, JC
    [J]. ATHEROSCLEROSIS, 1998, 141 (01) : 31 - 43
  • [3] IS VITAMIN-E THE ONLY LIPID-SOLUBLE, CHAIN-BREAKING ANTIOXIDANT IN HUMAN-BLOOD PLASMA AND ERYTHROCYTE-MEMBRANES
    BURTON, GW
    JOYCE, A
    INGOLD, KU
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1983, 221 (01) : 281 - 290
  • [4] Carr AC, 1999, AM J CLIN NUTR, V69, P1086
  • [5] Demonstration of rapid onset vascular endothelial dysfunction after hyperhomocysteinemia - An effect reversible with vitamin C therapy
    Chambers, JC
    McGregor, A
    Jean-Marie, J
    Obeid, OA
    Kooner, JS
    [J]. CIRCULATION, 1999, 99 (09) : 1156 - 1160
  • [6] FLOW STIMULATES ENDOTHELIAL-CELLS TO RELEASE A NITROVASODILATOR THAT IS POTENTIATED BY REDUCED THIOL
    COOKE, JP
    STAMLER, J
    ANDON, N
    DAVIES, PF
    MCKINLEY, G
    LOSCALZO, J
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (03): : H804 - H812
  • [7] N-Acetylcysteine does not influence the activity of endothelium-derived relaxing factor in vivo
    Creager, MA
    Roddy, MA
    Boles, K
    Stamler, JS
    [J]. HYPERTENSION, 1997, 29 (02) : 668 - 672
  • [8] Vascular function in the vitamin E-deprived rat - An interaction between nitric oxide and superoxide anions
    Davidge, ST
    Ojimba, J
    McLaughlin, MK
    [J]. HYPERTENSION, 1998, 31 (03) : 830 - 835
  • [9] DIEBERROTHENEDER M, 1991, J LIPID RES, V32, P1325
  • [10] Recovery by ascorbate of impaired nitric oxide-dependent relaxation resulting from oxidant stress in rat aorta
    Dudgeon, S
    Benson, DP
    MacKenzie, A
    Paisley-Zyszkiewicz, K
    Martin, W
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1998, 125 (04) : 782 - 786