Inhibitory effects of (-)-epigallocatechin gallate on the mutation, DNA strand cleavage, and DNA adduct formation by heterocyclic amines

被引:28
作者
Arimoto-Kobayashi, S [1 ]
Inada, N [1 ]
Sato, Y [1 ]
Sugiyama, C [1 ]
Okamoto, K [1 ]
Hayatsu, H [1 ]
Negishi, T [1 ]
机构
[1] Okayama Univ, Fac Pharmaceut Sci, Okayama 7008530, Japan
关键词
green tea; epigallocatechin gallate; heterocyclic arnines; DNA strand break; antimutagenicity; DNA adduct; Drosophila;
D O I
10.1021/jf0302761
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Green tea is known to be a potential chemopreventive agent against cancer. In this study, we investigated the inhibitory activities of tea extracts, and in particular the polyphenolic component (-)epigallocatechin gallate (EGCG), against heterocyclic amine-induced genotoxicity. The tea extracts displayed inhibition of 2-hydroxyamino-6-methyldipyrido[1,2-a,3',2'-d]imidazole (Glu-P-1(NHOH))-induced mutagenicity. This inhibition can be accounted for by the presence of EGCG in the extracts. The mutagenic effect of Glu-P-1 (NHOH), which induces single-strand cleavage in supercoiled circular DNA under neutral conditions, was inhibited by EGCG. Using the Drosophila repair test, a test for gross DNA damage, and DNA adduct detection by P-32-postlabeling, we showed that EGCG prevented 2-amino-3,8-dimethylimidazo[4,5-f]quinoline-induced DNA damage and adduct formation in insect DNA. EGCG was found to accelerate the degradation of Glu-P-1 (NHOH) in vitro. This observation suggested that the inhibition by EGCG is associated with an accelerated degradation of metabolically activated heterocyclic amines.
引用
收藏
页码:5150 / 5153
页数:4
相关论文
共 20 条
[1]   INHIBITORY EFFECT OF MYOGLOBIN AND HEMOGLOBIN ON THE DIRECT-ACTING MUTAGENICITY OF PROTEIN PYROLYSATE HETEROCYCLIC AMINE DERIVATIVES [J].
ARIMOTO, S ;
OHARA, Y ;
HIRAMOTO, K ;
HAYATSU, H .
MUTATION RESEARCH, 1987, 192 (04) :253-258
[2]   Inhibitory effects of beer and other alcoholic beverages on mutagenesis and DNA adduct formation induced by several carcinogens [J].
Arimoto-Kobayashi, S ;
Sugiyama, C ;
Harada, N ;
Takeuchi, M ;
Takemura, M ;
Hayatsu, H .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (01) :221-230
[3]  
Brown M D, 1999, Altern Med Rev, V4, P360
[4]   MARKED ANTIMUTAGENIC POTENTIAL OF AQUEOUS GREEN TEA EXTRACTS - MECHANISM OF ACTION [J].
BUABBAS, A ;
CLIFFORD, MN ;
WALKER, R ;
IOANNIDES, C .
MUTAGENESIS, 1994, 9 (04) :325-331
[5]   Induction of UDP-glucuronosyltransferase 1 (UDP-GT1) gene complex by green tea in male F344 rats [J].
Embola, CW ;
Sohn, OS ;
Fiala, ES ;
Weisburger, JH .
FOOD AND CHEMICAL TOXICOLOGY, 2002, 40 (06) :841-844
[6]  
FUJIKAWA K, 1988, J FOOD HYG SOC JPN, V29, P115
[7]   Cancer inhibition by green tea [J].
Fujiki, H ;
Suganuma, M ;
Okabe, S ;
Sueoka, N ;
Komori, A ;
Sueoka, E ;
Kozu, T ;
Tada, Y ;
Suga, K ;
Imai, K ;
Nakachi, K .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1998, 402 (1-2) :307-310
[8]   SUPPRESSION OF GENOTOXICITY OF CARCINOGENS BY (-)-EPIGALLOCATECHIN GALLATE [J].
HAYATSU, H ;
INADA, N ;
KAKUTANI, T ;
ARIMOTO, S ;
NEGISHI, T ;
MORI, K ;
OKUDA, T ;
SAKATA, I .
PREVENTIVE MEDICINE, 1992, 21 (03) :370-376
[9]   Effects of epigallocatechin gallate and quercetin on oxidative damage to cellular DNA [J].
Johnson, MK ;
Loo, G .
MUTATION RESEARCH-DNA REPAIR, 2000, 459 (03) :211-218
[10]  
MARON DM, 1984, HDB MUTAGENICITY TES, P93