Comparison of the chemopreventive potentials of melatonin and vitamin E plus selenium on 7,12-dimethylbenz[a]anthracene-induced inhibition of mouse liver antioxidant enzymes

被引:16
作者
Batcioglu, K
Karagözler, AA
Genç, M
Çelik, S
机构
[1] Adnan Menderes Univ, Fac Arts & Sci, Dept Chem, Div Biochem, TR-09010 Aydin, Turkey
[2] Inonu Univ, Fac Educ, Dept Chem Educ, TR-44069 Malatya, Turkey
[3] Inonu Univ, Sch Med, Dept Publ Hlth, TR-44069 Malatya, Turkey
[4] Firat Univ, Fac Arts & Sci, Dept Chem, Div Biochem, Elazig, Turkey
关键词
chemoprevention; DMBA; melatonin; selenium; vitamin E;
D O I
10.1097/00008469-200202000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemoprevention is a rapidly growing area of oncology that is identifying agents with a potentially preventive role in cancer. In this study, it was our goal to compare the chemopreventive effects of vitamin E plus selenium, and melatonin. Forty female mice were divided into four equal groups. The first group served as control. The second group had i.p. injections of 7,12-dimethylbenz[a]anthracene (DMBA) (20 mg/kg body weight) in corn oil for 21 days. The third group had the same procedure of DMBA injections as the second group and received vitamin E + selenium (90 mug + 1.8 mug/day), simultaneously. The fourth group had DMBA injections and melatonin (4.2 mg/kg body weight), simultaneously. DMBA alone caused significant inhibition of hepatic glutathione peroxidase (GSHPx), catalase (CAT), and superoxide dismutase (SOD) in the second group. In the third group, vitamin E + selenium restored DMBA-induced GSHPx inhibition significantly whereas CAT and SOD inhibition remained essentially unchanged. In the fourth group, melatonin not only significantly decreased DMBA-induced GSHPx inhibition but also fully reversed CAT and SOD inhibitions caused by DMBA. We speculate that melatonin alone provides better chemoprevention against DMBA-induced oxidative stress than the vitamin E + selenium combination. (C) 2002 Lippincott Williams Wilkins.
引用
收藏
页码:57 / 61
页数:5
相关论文
共 28 条
[1]  
Andersen HR, 1997, CLIN CHEM, V43, P562
[2]  
Arivazhagan K, 1997, CELL BIOCHEM FUNCT, V15, P15
[3]   EFFECT OF THE MAMMARY CARCINOGEN 7,12-DIMETHYLBENZ[A]ANTHRACENE ON PINEAL MELATONIN BIOSYNTHESIS, SECRETION AND PERIPHERAL METABOLISM [J].
BARTSCH, C ;
BARTSCH, H ;
LIPPERT, TH ;
GUPTA, D .
NEUROENDOCRINOLOGY, 1990, 52 (06) :538-544
[4]   SUPEROXIDE-DISMUTASE, GLUTATHIONE-PEROXIDASE AND CATALASE IN THE RED-CELLS OF PATIENTS WITH MALIGNANT-LYMPHOMA [J].
BEWICK, M ;
COUTIE, W ;
TUDHOPE, GR .
BRITISH JOURNAL OF HAEMATOLOGY, 1987, 65 (03) :347-350
[5]  
BLOCH B, 1921, SCHWEIZ MED WOSCHSCH, V5, P1033
[6]  
Bukin Y. V., 1999, Antioxidants in human health and disease., P235
[7]   ROLE OF RADICAL CATIONS IN AROMATIC HYDROCARBON CARCINOGENESIS [J].
CAVALIERI, E ;
ROGAN, E .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1985, 64 :69-84
[8]  
Cavalieri E., 1978, CARCINOG COMPR SURV, V3, P273
[9]  
CAVALIERI E, 1992, PHARMACOL THERAPEUT, V55, P182
[10]  
COLES C, 1992, CANCER RES, V52, P5291