DIFFERENTIAL STABILITY OF DRUG-METABOLIZING ENZYME-ACTIVITIES IN PRIMARY RAT HEPATOCYTES, CULTURED IN THE ABSENCE OR PRESENCE OF DEXAMETHASONE

被引:39
作者
MCMILLAN, JM
SHADDOCK, JG
CASCIANO, DA
ARLOTTO, MP
LEAKEY, JEA
机构
[1] NATL CTR TOXICOL RES,DIV REPROD & DEV TOXICOL,JEFFERSON,AR 72079
[2] NATL CTR TOXICOL RES,DIV GENET TOXICOL,JEFFERSON,AR 72079
[3] UNIV ARKANSAS MED SCI HOSP,DEPT PHARMACOL & INTERDISCIPLINARY TOXICOL,LITTLE ROCK,AR 72205
来源
MUTATION RESEARCH | 1991年 / 249卷 / 01期
关键词
HEPATOCYTE CULTURE; DRUG-METABOLIZING ENZYMES; DEXAMETHASONE; MONOOXYGENASE; CYTOCHROME-P450-DEPENDENT;
D O I
10.1016/0027-5107(91)90134-A
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The effects of primary hepatocyte culture on the rat cytochrome P450-dependent monooxygenase system and several conjugating enzyme activities were examined using a culture system similar to those used for evaluation of chemicals as potential genotoxins. Cytochrome P450 and cytochrome b5 contents progressively decreased throughout the 72-h culture period to < 25% of initial values, whereas cytochrome P450 reductase rapidly decreased by 50% during attachment, but then remained stable. Cytochrome P450-dependent testosterone hydroxylase activities decreased more rapidly in culture than did cytochrome P450 content reaching < 50% of attachment levels by 24 h. Cytochrome P450IIIA immunoreactive protein decreased at a similar rate to testosterone-6-beta-hydroxylase. Activated UDP-glucuronyltransferase activities towards 1-naphthol and testosterone declined more slowly over the 72 h than cytochrome P450 and remained at 50-60% of initial values at 72 h. UDP-glucuronyltransferase activity towards digitoxigenin monodigitoxoside (DIG) did not decrease during culture. Glutathione-S-transferase and sulfotransferase activities also declined during the 72 h at rates which appeared to be isozyme-dependent. Addition of 1-mu-M dexamethasone (DEX) to the culture medium increased UDP-glucuronyltransferase activity towards DIG, cytochrome P450 reductase and testosterone-6-beta-hydroxylase activities up to 2.5-, 2.0- and 7-fold, respectively and induced cytochrome P450IIIA immunoreactive protein(s) in the hepatocytes after 24 and 48 h of culture; DEX was less effective at the 72 h time-point. DEX treatment also significantly accelerated the decreases in glutathione-S-transferase activities and in sulfotransferase activities towards 1-naphthol and estrone. Thus, ii-appears that primary rat hepatocytes cultured under standard conditions, not only rapidly lose their monooxygenase capabilities, but also some of their capacity for conjugation.
引用
收藏
页码:81 / 92
页数:12
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