Phenolic Michael reaction acceptors: Combined direct and indirect antioxidant Defenses against electrophiles and oxidants

被引:47
作者
Dinkova-Kostova, A. T. [1 ,2 ]
Cheah, J.
Samouilov, A. [3 ,4 ,5 ]
Zweier, J. L. [4 ,5 ]
Bozak, R. E. [6 ]
Hicks, R. J. [6 ]
Talalay, P. [2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Clin Pharmacol, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Lewis B & Dorothy Cullman Canc Chemoprotect Ctr, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21287 USA
[4] Ohio State Univ, Coll Med & Publ Hlth, Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
[5] Ohio State Univ, Coll Med & Publ Hlth, Dept Internal Med, Columbus, OH 43210 USA
[6] Calif State Univ Hayward, Dept Chem, Hayward, CA 94542 USA
关键词
ABTS radical; direct antioxidant; indirect antioxidant; phase; 2; inducer; phenolic Michael acceptor; phenoxyl radical; galvinoxyl radical; glutathione;
D O I
10.2174/157340607780620680
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The implications of oxidative stress in the pathogenesis of many chronic human diseases has led to the widely accepted view that low molecular weight antioxidants could be beneficial and postpone or even prevent these diseases. Small molecules of either plant or synthetic origins, which contain Michael acceptor functionalities (olefins or acetylenes conjugated to electron-withdrawing groups) protect against the toxicity of oxidants and electrophiles indirectly, i.e., by inducing phase 2 cytoprotective enzymes. Some of these molecules, e. g., flavonoid and curcuminoid analogues that have phenolic hydroxyl groups in addition to Michael acceptor centers, are also potent direct antioxidants, and may therefore be appropriately designated: bifunctional antioxidants. By use of spectroscopic methods we identified phenolic chalcone and bis(benzylidene) acetone analogues containing one or two Michael acceptor groups, respectively, as very efficient scavengers of two different types of radicals: (a) the nitrogen-centered 2,2'-azinobis-(3-ethyl-benzothiazoline-6-sulfonic acid) (ABTS(center dot+)) radical cation, and (b) the oxygen-centered galvinoxyl (phenoxyl) radical. The most potent scavengers are those also bearing hydroxyl substituents on the aromatic ring(s) at the ortho-position(s). The initial reaction velocities are very rapid and concentration-dependent. In the human keratinocyte cell line HaCaT, the same compounds coordinately increase the intracellular levels of glutathione, glutathione reductase, and thioredoxin reductase. Thus, such bifunctional antioxidants could exert synergistic protective effects against oxidants and electrophiles which represent the principal biological hazards by: (i) scavenging hazardous oxidants directly and immediately; and (ii) inducing the phase 2 response to prevent and resolve the consequences of hazardous processes that are already in progress, i. e., acting indirectly, but with much more diverse and long-lasting effects.
引用
收藏
页码:261 / 268
页数:8
相关论文
共 49 条
[11]   The role of Keap1 in cellular protective responses [J].
Dinkova-Kostova, AT ;
Holtzclaw, WD ;
Kensler, TW .
CHEMICAL RESEARCH IN TOXICOLOGY, 2005, 18 (12) :1779-1791
[12]   Chemoprotective properties of phenylpropenoids, bis(benzylidene)cycloalkanones, and related Michael reaction acceptors: Correlation of potencies as phase 2 enzyme inducers and radical scavengers [J].
Dinkova-Kostova, AT ;
Abeygunawardana, C ;
Talalay, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (26) :5287-5296
[13]   Inhibition of the mutagenicity of 2-nitrofluorene, 3-nitrofluoranthene and 1-nitropyrene by flavonoids, coumarins, quinones and other phenolic compounds [J].
Edenharder, R ;
Tang, X .
FOOD AND CHEMICAL TOXICOLOGY, 1997, 35 (3-4) :357-372
[14]  
Eftekharpour E, 2000, GLIA, V31, P241, DOI 10.1002/1098-1136(200009)31:3<241::AID-GLIA50>3.0.CO
[15]  
2-9
[16]  
Gardner PT, 1998, J SCI FOOD AGR, V76, P257, DOI [10.1002/(SICI)1097-0010(199802)76:2<257::AID-JSFA944>3.0.CO
[17]  
2-B, 10.1002/(SICI)1097-0010(199802)76:2&lt
[18]  
257::AID-JSFA944&gt
[19]  
3.0.CO
[20]  
2-B]