Serum testosterone is reduced following short-term phytofluene, lycopene, or tomato powder consumption in F344 rats

被引:47
作者
Campbell, Jessica K. [1 ]
Stroud, Chad K. [1 ]
Nakamura, Manabu T. [1 ]
Lila, Mary Ann [1 ]
Erdman, John W., Jr. [1 ]
机构
[1] Univ Illinois, Div Nutr Sci, Urbana, IL 61801 USA
关键词
D O I
10.1093/jn/136.11.2813
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
Elevated serum androgens are associated with increased prostate cancer risk. Tomato consumption is also associated with reduced prostate cancer incidence, and the primary tomato carotenoid, lycopene, may modulate androgen activation in the prostate, yet little is known about other tomato carotenoids. To evaluate interrelations between phytofluene, lycopene, or tomato powder consumption and androgen status, 8-wk-old male F344 rats (fed a control AIN 93G diet) were castrated or sham-operated and subsequently provided with daily oral supplementation of phytofluene or lycopene (similar to 0.7 mg/d) or fed a 10% tomato powder supplemented diet (AIN 93G) for 4 d. Sham-operated rats provided with either phytofluene, lycopene, or tomato powder had similar to 40-50% lower serum testosterone concentrations than the sham-operated, control-fed group. Tissue and serum phytofluene and lycopene concentrations were greater in castrated rats than in sham-operated rats, which may have been due in part to a decrease of hepatic CYP 3A1 mRNA expression and benzyloxyresorufin-O-dealkylase activity. Some changes in prostatic and testicular steroidogenic enzyme mRNA expression were found; in particular, prostate 17 beta-hydroxysteroid dehydrogenase 4 mRNA expression in castrated rats fed lycopene or tomato powder was 1.7-fold that of the sham-operated, control-fed group. Modest changes in mRNA expression of steroidogenic enzymes with short-term carotenoid intake may alter the flux of androgen synthesis to less potent compounds. Overall, results illustrate that short-term intake of tomato carotenoids significantly alters androgen status, which may partially be a mechanism by which tomato intake reduces prostate cancer risk.
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收藏
页码:2813 / 2819
页数:7
相关论文
共 56 条
[31]  
Kucuk O, 2001, CANCER EPIDEM BIOMAR, V10, P861
[32]   INTERACTION OF ANTICANCER DRUGS WITH HEPATIC MONOOXYGENASE ENZYMES [J].
LEBLANC, GA ;
WAXMAN, DJ .
DRUG METABOLISM REVIEWS, 1989, 20 (2-4) :395-439
[33]   CLINICAL AND BIOCHEMICAL PARAMETERS OF ANDROGEN ACTION IN NORMAL HEALTHY CAUCASIAN VERSUS CHINESE SUBJECTS [J].
LOOKINGBILL, DP ;
DEMERS, LM ;
WANG, C ;
LEUNG, A ;
RITTMASTER, RS ;
SANTEN, RJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 72 (06) :1242-1248
[34]   Tomato products, lycopene, and prostate cancer risk [J].
Miller, EC ;
Giovannucci, E ;
Erdman, JW ;
Bahnson, R ;
Schwartz, SJ ;
Clinton, SK .
UROLOGIC CLINICS OF NORTH AMERICA, 2002, 29 (01) :83-+
[35]   Effects of ligand activation of peroxisome proliferator-activated receptor γ in human prostate cancer [J].
Mueller, E ;
Smith, M ;
Sarraf, P ;
Kroll, T ;
Aiyer, A ;
Kaufman, DS ;
Oh, W ;
Demetri, G ;
Figg, WD ;
Zhou, XP ;
Eng, C ;
Spiegelman, BM ;
Kantoff, PW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (20) :10990-10995
[36]   THE P450 SUPERFAMILY - UPDATE ON NEW SEQUENCES, GENE-MAPPING, ACCESSION NUMBERS, EARLY TRIVIAL NAMES OF ENZYMES, AND NOMENCLATURE [J].
NELSON, DR ;
KAMATAKI, T ;
WAXMAN, DJ ;
GUENGERICH, FP ;
ESTABROOK, RW ;
FEYEREISEN, R ;
GONZALEZ, FJ ;
COON, MJ ;
GUNSALUS, IC ;
GOTOH, O ;
OKUDA, K ;
NEBERT, DW .
DNA AND CELL BIOLOGY, 1993, 12 (01) :1-51
[37]   In vitro metabolism of midazolam, triazolam, nifedipine, and testosterone by human liver microsomes and recombinant cytochromes P450: Role of CYP3A4 and CYP3A5 [J].
Patki, KC ;
von Moltke, LL ;
Greenblatt, DJ .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (07) :938-944
[38]   Activation of peroxisome proliferator-activated receptor (PPAR)-gamma by 15S-hydroxyeicosatrienoic acid parallels growth suppression of androgen-dependent prostatic adenocarcinoma cells [J].
Pham, H ;
Banerjee, T ;
Nalbandian, GM ;
Ziboh, VA .
CANCER LETTERS, 2003, 189 (01) :17-25
[39]   A RAPID METHOD FOR ASSAYING THE METABOLISM OF 7-ETHOXYRESORUFIN BY MICROSOMAL SUBCELLULAR-FRACTIONS [J].
POHL, RJ ;
FOUTS, JR .
ANALYTICAL BIOCHEMISTRY, 1980, 107 (01) :150-155
[40]   AIN-93 PURIFIED DIETS FOR LABORATORY RODENTS - FINAL REPORT OF THE AMERICAN INSTITUTE OF NUTRITION AD HOC WRITING COMMITTEE ON THE REFORMULATION OF THE AIN-76A RODENT DIET [J].
REEVES, PG ;
NIELSEN, FH ;
FAHEY, GC .
JOURNAL OF NUTRITION, 1993, 123 (11) :1939-1951