Lycopene and β-carotene protect in vivo iron-induced oxidative stress damage in rat prostate

被引:44
作者
Matos, HR
Marques, SA
Gomes, OF
Silva, AA
Heimann, JC
Di Mascio, P
Medeiros, MHG
机构
[1] Univ Sao Paulo, Inst Quim, Dept Bioquim, BR-05508900 Sao Paulo, Brazil
[2] Univ Sao Paulo, Fac Med, Dept Clin Med Nefrol, BR-05508900 Sao Paulo, Brazil
[3] Univ Fed Sergipe, Dept Fisiol, Sao Cristovao, SE, Brazil
关键词
lycopene; beta-carotene; DNA damage; 8-oxo-7,8-dihydro-2 '-deoxyguanosine; ferric nitrilotriacetate; prostate cancer;
D O I
10.1590/S0100-879X2006000200006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
It has been suggested that iron overload may be carcinogenic. In the present study, we evaluated the effect of plasma and prostate carotenoid concentration on oxidative DNA damage in 12-week-old Wistar rats treated with intraperitoneal (ip) ferric nitrilotriacetate (Fe-NTA) (10 mg Fe/kg). Plasma ss-carotene and lycopene concentrations were measured as a function of time after ip injection of carotenoids (10 mg kg(-1) day(-1) s-carotene or lycopene) in rats. The highest total plasma concentration was reached 3 and 6 h after ip injection of lycopene or ss-carotene, respectively. After 5 days of carotenoid treatment, lycopene and B-carotene were present in the 0.10-0.51 nmol/g wet tissue range in the prostate. Using a sensitive method to detected 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodGuo) by HPLC/EC, the level of 8-oxodGuo in rat prostate DNA was significantly higher (6.3 +/- 0.6 residues/10(6) dGuo) 3 h after Fe-NTA injection compared with control rats (1.7 +/- 0.3 residues/10(6) dGuo). Rats supplemented with lycopene or B-carotene for 5 days prior to Fe-NTA treatment showed a reduction of about 70% in 8-oxodGuo levels to almost control levels. Compared with control rats, the prostate of Fe-NTA-treated animals showed a 78% increase in malondialdehyde accumulation. Lycopene or ss-carotene pre-treatment almost completely prevented lipid damage. Epidemiological studies have suggested a lower risk of prostate cancer in men reporting a higher consumption of tomato products. However, before associating this effect with tomato sauce constituents, more information is required. The results described here may contribute to the understanding of the protective effects of carotenoids against iron-induced oxidative stress.
引用
收藏
页码:203 / 210
页数:8
相关论文
共 39 条
[1]   THE CAUSES AND PREVENTION OF CANCER [J].
AMES, BN ;
GOLD, LS ;
WILLETT, WC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5258-5265
[2]   DIETARY CARCINOGENS AND ANTICARCINOGENS - OXYGEN RADICALS AND DEGENERATIVE DISEASES [J].
AMES, BN .
SCIENCE, 1983, 221 (4617) :1256-1264
[3]   Lycopene oxidation product enhances gap junctional communication [J].
Aust, O ;
Ale-Agha, N ;
Zhang, L ;
Wollersen, H ;
Sies, H ;
Stahl, W .
FOOD AND CHEMICAL TOXICOLOGY, 2003, 41 (10) :1399-1407
[4]  
BATES GW, 1973, J BIOL CHEM, V248, P3228
[5]   Prostate carcinogenesis in N-methyl-N-nitrosourea (NMU)-testosterone-treated rats fed tomato powder, lycopene, or energy-restricted diets [J].
Boileau, TWM ;
Liao, ZM ;
Kim, S ;
Lemeshow, S ;
Erdman, JW ;
Clinton, SK .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (21) :1578-1586
[6]   Liver iron excess in patients with hepatocellular carcinoma developed on viral C cirrhosis [J].
Chapoutot, C ;
Esslimani, M ;
Joomaye, Z ;
Ramos, J ;
Perney, P ;
Laurent, C ;
Fabbro-Peray, P ;
Larrey, D ;
Domergue, J ;
Blanc, F .
GUT, 2000, 46 (05) :711-714
[7]   Oxidative DNA damage in prostate cancer patients consuming tomato sauce-based entrees as a whole-food intervention [J].
Chen, LW ;
Stacewicz-Sapuntzakis, M ;
Duncan, C ;
Sharifi, R ;
Ghosh, L ;
van Breemen, R ;
Ashton, D ;
Bowen, PE .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (24) :1872-1879
[8]   LYCOPENE AS THE MOST EFFICIENT BIOLOGICAL CAROTENOID SINGLET OXYGEN QUENCHER [J].
DI MASCIO, P ;
KAISER, S ;
SIES, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1989, 274 (02) :532-538
[9]   Role of oxygen free radicals in cancer development [J].
Dreher, D ;
Junod, AF .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (01) :30-38
[10]  
EBINA Y, 1986, J NATL CANCER I, V76, P107