Do antioxidants impair signaling by reactive oxygen species and lipid oxidation products?

被引:119
作者
Niki, Etsuo [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Hlth Res Inst, Ikeda, Osaka 5638577, Japan
关键词
Adaptive response; Antioxidant; Lipid peroxidation; Oxidative stress; Reactive oxygen species; Signaling; PC12 CELL TOLERANCE; FATTY LIVER-DISEASE; ADAPTIVE RESPONSE; GENE-EXPRESSION; FREE-RADICALS; PEROXIDATION; MECHANISMS; INDUCTION; NRF2; TRANSDUCTION;
D O I
10.1016/j.febslet.2012.09.025
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
Oxidative modification of biologically essential molecules by reactive oxygen and nitrogen species (ROS/RNS) has been implicated in the pathogenesis of various diseases. At the same time, roles of ROS/RNS as physiological signaling messenger have been established. Lipid oxidation products also have two faces. It is argued that the radical scavenging antioxidants taken from diet or supplement may impair such beneficial effects of ROS/RNS and lipid oxidation products. However, it is unlikely that antioxidants impair physiologically important signaling, since the antioxidants do not scavenge signaling ROS/RNS nor do they inhibit the formation of signaling molecules. Lipid peroxidation products are not produced on purpose and inhibition of lipid peroxidation by antioxidants should be beneficial for maintenance of health and reducing disease risk. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:3767 / 3770
页数:4
相关论文
共 49 条
[1]   Oxidative stress: A dead end or a laboratory hypothesis? [J].
Azzi, Angelo .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 362 (02) :230-232
[2]   Rediscovery of cerebrosterol [J].
Bjorkhem, Ingemar .
LIPIDS, 2007, 42 (01) :5-14
[3]   An integrated omics analysis of eicosanoid biology [J].
Buczynski, Matthew W. ;
Dumlao, Darren S. ;
Dennis, Edward A. .
JOURNAL OF LIPID RESEARCH, 2009, 50 (06) :1015-1038
[4]   Adaptive response induced by lipid peroxidation products in cell cultures [J].
Chen, ZH ;
Yoshida, Y ;
Saito, Y ;
Noguchi, N ;
Niki, E .
FEBS LETTERS, 2006, 580 (02) :479-483
[5]   4-Hydroxynonenal induces adaptive response and enhances PC12 cell tolerance primarily through induction of thioredoxin reductase 1 via activation of Nrf2 [J].
Chen, ZH ;
Saito, Y ;
Yoshida, Y ;
Sekine, A ;
Noguchi, N ;
Niki, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (51) :41921-41927
[6]   Induction of Adaptive Response and Enhancement of PC12 Cell Tolerance by 7-Hydroxycholesterol and 15-Deoxy-Δ12,14-Prostaglandin J2 through Up-regulation of Cellular Glutathione via Different Mechanisms [J].
Chen, Zhi-Hua ;
Yoshida, Yasukazu ;
Saito, Yoshiro ;
Sekine, Azusa ;
Noguchi, Noriko ;
Niki, Etsuo .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (20) :14440-14445
[7]  
Cochemé HM, 2010, CURR OPIN INVEST DR, V11, P426
[8]   Vitamin E and Risk of Cardiovascular Diseases: A Review of Epidemiologic and Clinical Trial Studies [J].
Cordero, Zorabel ;
Drogan, Dagmar ;
Weikert, Cornelia ;
Boeing, Heiner .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 2010, 50 (05) :420-440
[9]   Myeloperoxidase-derived oxidation: mechanisms of biological damage and its prevention [J].
Davies, Michael J. .
JOURNAL OF CLINICAL BIOCHEMISTRY AND NUTRITION, 2011, 48 (01) :8-19
[10]   F2-isoprostanes as an indicator and risk factor for coronary heart disease [J].
Davies, Sean S. ;
Roberts, L. Jackson, II .
FREE RADICAL BIOLOGY AND MEDICINE, 2011, 50 (05) :559-566