Phytoene, phytofluene, and lycopene from tomato powder differentially accumulate in tissues of male Fisher 344 rats

被引:39
作者
Campbell, Jessica K. [1 ]
Engelmann, Nancy J. [1 ]
Lila, Mary Ann [1 ]
Erdman, John W., Jr. [1 ]
机构
[1] Univ Illinois, Div Nutr Sci, Urbana, IL 61801 USA
基金
美国国家卫生研究院;
关键词
carotenoids; phytoene; phytofluene; lycopene; prostate cancer; rats;
D O I
10.1016/j.nutres.2007.09.015
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Tomato product consumption is inversely related to prostate cancer incidence, and lycopene (LYC) has been implicated in reduced prostate cancer risk. The contribution of other tomato carotenoids, phytoene (PE) and phytofluene (PF), toward prostate cancer risk has not been adequately studied. The relative uptake and tissue distribution of tomato carotenoids are not known. We hypothesize that PE and PF are bioavailable from a tomato powder diet or from a purified source and accumulate in androgen-sensitive tissues. In this study, 4-week-old male Fisher 344 rats (Harlan, Indianapolis, Ind) were prefed an AIN-93G powder diet composed of 10140 tomato powder containing PE, PF, and LYC (0.015, 0.012, and 0.011 g/kg diet, respectively). After 30-day tomato powder feeding, hepatic PF concentrations (168 +/- 20 nmol/g) were higher than PE or LYC (104 +/- 13 and 104 +/- 13 nmol/g, respectively). In contrast, LYC, followed by PF, had the highest accumulation of the measured carotenoids in the prostate lobes and seminal vesicles. When tomato powder-fed rats received a single oral dose of either approximately 2.7 mg PE or approximately 2.7 mg PF, an increase in the dosed carotenoid concentration was observed in all measured tissues, except in the adrenal. The percentages of increases of PF were greater than that of PE in liver, serum, and adipose (37%, 287%, and 49% vs 16%, 179%, and 23%, respectively). Results indicate that the relative tomato-carotenoid biodistribution differs in liver and androgen-sensitive tissues, suggesting that minor changes in the number of sequential double bonds in carotenoid structures alter absorption and/or metabolism of tomato carotenoids. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:794 / 801
页数:8
相关论文
共 46 条
[1]   Identification of scavenger receptor SR-BI as a high density lipoprotein receptor [J].
Acton, S ;
Rigotti, A ;
Landschulz, KT ;
Xu, SZ ;
Hobbs, HH ;
Krieger, M .
SCIENCE, 1996, 271 (5248) :518-520
[2]  
*AM CANC SOC, CANC FACTS FIG 2006
[3]   IMMUNOCYTOCHEMICAL LOCALIZATION OF RAT INTESTINAL 15 KDA PROTEIN, A MEMBER OF CYTOPLASMIC FATTY ACID-BINDING PROTEINS [J].
AMANO, O ;
KANDA, T ;
ONO, T ;
ISEKI, S .
ANATOMICAL RECORD, 1992, 234 (02) :215-222
[4]   Identification and characterization of a Pi isoform of glutathione S-transferase (GSTP1) as a zeaxanthin-binding protein in the macula of the human eye [J].
Bhosale, P ;
Larson, AJ ;
Frederick, JM ;
Southwick, K ;
Thulin, CD ;
Bernstein, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (47) :49447-49454
[5]   FRUIT, VEGETABLES, AND CANCER PREVENTION - A REVIEW OF THE EPIDEMIOLOGIC EVIDENCE [J].
BLOCK, G ;
PATTERSON, B ;
SUBAR, A .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1992, 18 (01) :1-29
[6]   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
[7]   Bioavailability of all-trans and cis-isomers of lycopene [J].
Boileau, TWM ;
Boileau, AC ;
Erdman, JW .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2002, 227 (10) :914-919
[8]   Testosterone and food restriction modulate hepatic lycopene isomer concentrations in male F344 rats [J].
Boileau, TWM ;
Clinton, SK ;
Zaripheh, S ;
Monaco, MH ;
Donovan, SM ;
Erdman, JW .
JOURNAL OF NUTRITION, 2001, 131 (06) :1746-1752
[9]   Tissue lycopene concentrations and isomer patterns are affected by androgen status and dietary lycopene concentration in male F344 rats [J].
Boileau, TWM ;
Clinton, SK ;
Erdman, JW .
JOURNAL OF NUTRITION, 2000, 130 (06) :1613-1618
[10]   Use of animal models in defining efficacy of chemoprevention agents against prostate cancer [J].
Bosland, MC .
EUROPEAN UROLOGY, 1999, 35 (5-6) :459-463