Mechanism(s) of turmeric-mediated protective effects against benzo(a)pyrene-derived DNA adducts

被引:35
作者
Thapliyal, R [1 ]
Deshpande, SS [1 ]
Maru, GB [1 ]
机构
[1] Tata Mem Hosp, Canc Res Inst, Div Carcinogenesis, Parel 400012, Mumbai, India
关键词
benzo(a)pyrene; DNA adducts; CYP1A1; CYP1A2; turmeric-mediated inhibition; mouse tissues;
D O I
10.1016/S0304-3835(01)00675-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effects of turmeric feeding before and after benzo(a)pyrene [B(a)P] exposure on the levels of B(a)P-derived DNA adducts were studied in tissues of Swiss mice employing P-32-postlabelling analysis. A reduction in the levels of B(a)P-derived DNA adducts in liver, lung, and forestomach was observed in animals pre-treated with 0.2 or 1% turmeric diet and exposed to B(a)P by oral intubation when compared to animals receiving standard laboratory diet and B(a)P. The observed decrease was not due to dilution caused by nascent DNA synthesis. Comparative evaluation of levels of B(a)P-derived DNA adducts in tissues of animals shifted to 0.2 or 1% turmeric diet after 24 It of oral intubation of B(a)P with those continued on standard laboratory diet did not suggest enhanced disappearance/repair of B(a)P-derived DNA adducts due to exposure to turmeric. Further, pre-treatment of mice with 1% turmeric diet significantly reduced the B(a)P-induced increase in activity of cytochrome P450 (CYP450) isozymes CYP 1A1 and 1A2 in liver, lung, and forestomach of mice. In addition, hepatic glutathione S-transferase (GST) was found to be elevated in turmeric pre-treated mice. Thus turmeric-mediated decrease in induction of phase-I enzymes in liver, lung, and forestomach of mice and enhancement of hepatic GST appear to play an important role in reducing the B(a)P-induced DNA damage in target and non-target tissues. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:79 / 88
页数:10
相关论文
共 32 条
[1]   METHODS FOR DETECTING CARCINOGENS AND MUTAGENS WITH SALMONELLA-MAMMALIAN-MICROSOME MUTAGENICITY TEST [J].
AMES, BN ;
MCCANN, J ;
YAMASAKI, E .
MUTATION RESEARCH, 1975, 31 (06) :347-363
[2]   PHARMACOLOGY OF CURCUMA-LONGA [J].
AMMON, HPT ;
WAHL, MA .
PLANTA MEDICA, 1991, 57 (01) :1-7
[3]   CHEMOPREVENTIVE EFFECT OF TURMERIC AGAINST STOMACH AND SKIN TUMORS INDUCED BY CHEMICAL CARCINOGENS IN SWISS MICE [J].
AZUINE, MA ;
BHIDE, SV .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1992, 17 (01) :77-83
[4]   Subchronic oral toxicity of turmeric and ethanolic turmeric extract in female mice and rats [J].
Deshpande, SS ;
Lalitha, VS ;
Ingle, AD ;
Raste, AS ;
Gadre, SG ;
Maur, GB .
TOXICOLOGY LETTERS, 1998, 95 (03) :183-193
[5]   Inhibitory effects of curcumin-free aqueous turmeric extract on benzo[a]pyrene-induced forestomach papillomas in mice [J].
Deshpande, SS ;
Ingle, AD ;
Maru, GB .
CANCER LETTERS, 1997, 118 (01) :79-85
[6]   EFFECTS OF CURCUMIN ON THE FORMATION OF BENZO[ALPHA]PYRENE DERIVED DNA-ADDUCTS IN-VITRO [J].
DESHPANDE, SS ;
MARU, GB .
CANCER LETTERS, 1995, 96 (01) :71-80
[7]   Chemopreventive efficacy of curcumin-free aqueous turmeric extract in 7,12-dimethylbenz[a]anthracene-induced rat mammary tumorigenesis [J].
Deshpande, SS ;
Ingle, AD ;
Maru, GB .
CANCER LETTERS, 1998, 123 (01) :35-40
[8]  
DESHPANDE SS, 1997, THESIS U MUMBAI MUMB
[9]   EFFECT OF TURMERIC ON XENOBIOTIC-METABOLIZING ENZYMES [J].
GOUD, VK ;
POLASA, K ;
KRISHNASWAMY, K .
PLANT FOODS FOR HUMAN NUTRITION, 1993, 44 (01) :87-92
[10]   TURMERIC - CHEMISTRY, TECHNOLOGY, AND QUALITY [J].
GOVINDARAJAN, VS .
CRC CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1980, 12 (03) :199-301