Punicalagin and Catechins Contain Polyphenolic Substructures That Influence Cell Viability and Can Be Monitored by Radical Chemosensors Sensitive to Electron Transfer

被引:9
作者
Carreras, Anna [1 ]
Luisa Mateos-Martin, Maria [1 ]
Velazquez-Palenzuela, Amado [2 ]
Brillas, Enric [2 ]
Cascante, Marta [3 ]
Julia, Luis [1 ]
Lluis Torres, Josep [1 ]
机构
[1] IQAC CSIC, Dept Biol Chem & Mol Modelling, Inst Adv Chem Catalonia, Barcelona 08034, Spain
[2] Univ Barcelona, Dept Phys Chem, E-08028 Barcelona, Spain
[3] Univ Barcelona, Dept Biochem & Mol Biol, Unit Associated CSIC, E-08028 Barcelona, Spain
关键词
punicalagin; catechins; pyrogallol; TNPTM chemosensor; cell viability; ANTIOXIDANT ACTIVITY; (-)-EPIGALLOCATECHIN GALLATE; DIETARY POLYPHENOLS; IN-VIVO; METABOLISM; FLAVAN-3-OLS; EPICATECHIN; SUPEROXIDE; EXTRACTS; CULTURE;
D O I
10.1021/jf204059x
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Plant polyphenols may be free radical scavengers or generators, depending on their nature and concentration. This dual effect, mediated by electron transfer reactions, may contribute to their influence on cell viability. This study used two stable radicals (tris(2,3,5,6-tetrachloro-4-nitrophenyl)methyl (TNPTM) and tris(2,4,6-trichloro-3,5-dinitrophenyl)methyl (HNTTM)) sensitive only to electron transfer reduction reactions to monitor the redox properties of polyphenols (punicalagin and catechins) that contain phenolic hydroxyls with different reducing capacities. The use of the two radicals reveals that punicalagin's substructures consisting of gallate esters linked together by carbon-carbon (C-C) bonds are more reactive than simple gallates and less reactive than the pyrogallol moiety of green tea catechins. The most reactive hydroxyls, detected by TNPTM, are present in the compounds that affect HT-29 cell viability the most. TNPTM reacts with C-C-linked gallates and pyrogallol and provides a convenient way to detect potentially beneficial polyphenols from natural sources.
引用
收藏
页码:1659 / 1665
页数:7
相关论文
共 35 条
[21]   Reducing activity of polyphenols with stable radicals of the TTM series.: Electron transfer versus H-abstraction reactions in flavan-3-ols [J].
Jiménez, A ;
Selga, A ;
Torres, JU ;
Julia, L .
ORGANIC LETTERS, 2004, 6 (24) :4583-4586
[22]   Scavenging mechanisms of (-)-epigallocatechin gallate and (-)-epicatechin gallate on peroxyl radicals and formation of superoxide during the inhibitory action [J].
Kondo, K ;
Kurihara, M ;
Miyata, N ;
Suzuki, T ;
Toyoda, M .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (7-8) :855-863
[23]   Epicatechin and catechin are O-methylated and glucuronidated in the small intestine [J].
Kuhnle, G ;
Spencer, JPE ;
Schroeter, H ;
Shenoy, B ;
Debnam, ES ;
Srai, SKS ;
Rice-Evans, C ;
Hahn, U .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 277 (02) :507-512
[24]   Possible controversy over dietary polyphenols: Benefits vs risks [J].
Lambert, Joshua D. ;
Sang, Shengmin ;
Yang, Chung S. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2007, 20 (04) :583-585
[25]   Chemical Methods To Evaluate Antioxidant Ability [J].
Liu, Zai-Qun .
CHEMICAL REVIEWS, 2010, 110 (10) :5675-5691
[26]   The importance of polymerization and galloylation for the antiproliferative properties of procyanidin-rich natural extracts [J].
Lizarraga, D. ;
Lozano, C. ;
Briede, J. J. ;
van Delft, J. H. ;
Tourino, S. ;
Centelles, J. J. ;
Torres, J. L. ;
Cascante, M. .
FEBS JOURNAL, 2007, 274 (18) :4802-4811
[27]   Artifacts in cell culture: Rapid generation of hydrogen peroxide on addition of (-)-epigallocatechin, (-)-epigallocatechin gallate, (+)-catechin, and quercetin to commonly used cell culture media [J].
Long, LH ;
Clement, MV ;
Halliwell, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (01) :50-53
[28]   Hormesis defined [J].
Mattson, Mark P. .
AGEING RESEARCH REVIEWS, 2008, 7 (01) :1-7
[29]   Activity of grape polyphenols as inhibitors of the oxidation of fish lipids and frozen fish muscle [J].
Pazos, M ;
Gallardo, JM ;
Torres, JL ;
Medina, I .
FOOD CHEMISTRY, 2005, 92 (03) :547-557
[30]   Ellagitannin chemistry. The first synthesis of dehydrohexahydroxydiphenoate esters from oxidative coupling of unetherified methyl gallate [J].
Quideau, S ;
Feldman, KS .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (25) :8809-8813