Effects of caloric restriction on expression of testicular cytochrome P450 enzymes associated with the metabolic activation of carcinogens

被引:30
作者
Seng, JE
Gandy, J
Turturro, A
Lipman, R
Bronson, RT
Parkinson, A
Johnson, W
Hart, RW
Leakey, JEA
机构
[1] NATL CTR TOXICOL RES,JEFFERSON,AR 72079
[2] UNIV ARKANSAS MED SCI HOSP,DEPT PHARMACOL TOXICOL,LITTLE ROCK,AR 72205
[3] UNIV KANSAS,MED CTR,CTR ENVIRONM & OCCUPAT HLTH,DEPT PHARMACOL TOXICOL & THERAPEUT,KANSAS CITY,KS 66160
[4] TUFTS UNIV,USDA,HUMAN NUTR RES CTR AGING,BOSTON,MA 02111
[5] US FDA,CTR FOOD SAFETY & APPL NUTR,LAUREL,MD 20708
关键词
dietary restriction; testes; cytochrome P450 monooxygenase; testosterone; 7; alpha-hydroxylase; CYP2A1; dealkylase; Leydig cell hyperplasia;
D O I
10.1006/abbi.1996.0480
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous work demonstrated that microsomal cytochrome P4502A1 (CYP2A1) is expressed in rat testicular Leydig cells. The present study investigates the effects of diet, age, and strain on rat testicular CYP2A1 expression and assesses the potential role of testicular CYP2A1 in the metabolic activation of carcinogens. In ad libitum-fed 18-week-old Fischer 344 rats, testicular CYP2A1 immunoreactive protein and testosterone 7 alpha-hydroxylase activity (7 alpha-TOHase) exhibited a circadian variation with a daytime maximum and a night-time minimum (82.2 +/- 42.0 and 21.9 +/- 4.5 pmol 7 alpha-hydroxytestosterone/min/mg protein, respectively). Caloric restriction (to 60% of ad libitum consumption), which reduces the severity of Leydig cell tumors in rats, decreased expression of both CYP2A1 and testicular 7 alpha-TOHase >80% and eliminated their circadian variation. Conversely, caloric restriction induced a circadian rhythm in testicular 7-benzyloxyresorufin-O-dealkylase activity. Testicular microsomes from ad libitum-fed rats having peak diurnal 7 alpha-TOHase activity had significantly greater (30%) microsome-mediated aflatoxin B-1-DNA binding activity compared to microsomes prepared from nocturnal phase ad libitum-fed or calorically restricted rats which expressed low 7 alpha-TOHase activity. In 12-month-old Fischer 344 rats, high CYP2A1 expression was correlated with severe Leydig cell hyperplasia (r = 0.80), whereas CYP2A immunoreactive protein and 7 alpha-TOHase were expressed at lower levels in Sprague-Dawley than in Fischer 344 rats and were undetectable in pig, monkey, and human testes. These are strains/species that do not exhibit significant Leydig cell hyperplasia. This suggests that caloric intake, strain, and circadian factors may all mediate testicular CYP2A1 expression in the rat and that CYP2A1 may in turn influence carcinogen activation and pathological status in the testis.
引用
收藏
页码:42 / 52
页数:11
相关论文
共 59 条
[21]   HYDROXYLATION OF 5-ALPHA-ANDROSTANE-3-BETA, 17-BETA-DIOL BY RAT PROSTATE MICROSOMES - EFFECTS OF ANTIBODIES AND CHEMICAL INHIBITORS OF CYTOCHROME-P450 ENZYMES [J].
GEMZIK, B ;
GREEN, J ;
PARKINSON, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 296 (02) :355-365
[22]   EVIDENCE FOR A FREE-RADICAL-DEPENDENT METABOLISM OF 7,12-DIMETHYLBENZ(A)ANTHRACENE IN RAT TESTIS [J].
GEORGELLIS, A ;
MONTELIUS, J ;
RYDSTROM, J .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1987, 87 (01) :141-154
[23]   CELL-SPECIFIC METABOLIC-ACTIVATION OF 7,12-DIMETHYLBENZ[A]ANTHRACENE IN RAT TESTIS [J].
GEORGELLIS, A ;
RYDSTROM, J .
CHEMICO-BIOLOGICAL INTERACTIONS, 1989, 72 (1-2) :65-78
[24]  
GONZALEZ FJ, 1989, PHARMACOL REV, V40, P243
[25]   ENZYMATIC ACTIVATION OF CHEMICALS TO TOXIC METABOLITES [J].
GUENGERICH, FP ;
LIEBLER, DC .
CRC CRITICAL REVIEWS IN TOXICOLOGY, 1985, 14 (03) :259-307
[26]   CALORIC RESTRICTION AND TOXICITY [J].
HART, RW ;
KEENAN, K ;
TURTURRO, A ;
ABDO, KM ;
LEAKEY, J ;
LYNCOOK, B .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1995, 25 (02) :184-195
[27]   CYTOCHROME-P-450 CHOLESTEROL 7-ALPHA-HYDROXYLASE - INHIBITION OF ENZYME DEACTIVATION BY STRUCTURALLY DIVERSE CALMODULIN ANTAGONISTS AND PHOSPHATASE INHIBITORS [J].
HOLSZTYNSKA, EJ ;
WAXMAN, DJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 256 (02) :543-559
[28]  
KAMATAKI T, 1985, J PHARMACOL EXP THER, V233, P222
[29]  
Labecque G, 1991, PHARMACOL THERAPEUT, V52, P95
[30]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+