Inhibition of xenobiotic-induced genotoxicity in cultured precision-cut human and rat liver slices

被引:35
作者
Lake, BG
Beamand, JA
Tredger, JM
Barton, PT
Renwick, AB
Price, RJ
机构
[1] British Ind Biol Res Assoc, Carshalton SM5 4DS, Surrey, England
[2] Kings Coll Hosp, Sch Med & Dent, Inst Liver Studies, London SE5 9PJ, England
关键词
2-acetylaminofluorene; aflatoxin B-1; 2-amino-1-methyl-6-phenylimidazo [4,5-b]pyridine; flavonoids; precision-cut human and rat liver slice; tangeretin; unscheduled DNA synthesis;
D O I
10.1016/S1383-5718(99)00010-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this study precision-cut liver slices have been used to evaluate the effects of the flavone tangeretin, the flavonoid glycoside naringin and the flavanone naringenin (the aglycone derived from naringin) on xenobiotic-induced genotoxicity. Liver slices were cultured for 24 h in medium containing [H-3]thymidine and the test compounds and then processed for autoradiographic determination of unscheduled DNA synthesis (UDS). The cooked food mutagen 2-amino-1-methyyl-6-phenylimidazo[4,5-b]pyridine (PhIP) markedly induced UDS in cultured human liver slices and both 2-acetylaminofluorene (2-AAF) and aflatoxin B-1 (AFB(1)) induced UDS in cultured rat liver slices. Tangeretin (20 and 50 mu M) was found to be a potent inhibitor of 5 and 50 mu M PhIP-induced UDS in human liver slices, whereas 20 and 50 mu M naringenin was ineffective and naringin only inhibited genotoxicity at a concentration of 1000 mu M. In rat liver slices 50 mu M tangeretin inhibited 10 and 50 mu M 2-AAF-induced UDS, whereas 50 mu M naringenin and 100 and 1000 mu M naringin were ineffective. None of the three flavonoids examined inhibited 5 mu M AFB(1)-induced UDS in rat liver slices. The inhibition of PhIP- and 2-AAF-induced UDS by tangeretin is probably attributable to the inhibition of the human and rat cytochrome P-450 isoforms which are responsible for the bioactivation of these two genotoxins. Although flavonoids can modulate xenobiotic-induced genotoxicity in human and rat liver slices, any protective effect is dependent on the particular combination of genotoxin and flavonoid examined. These results demonstrate that cultured precision-cut liver slices may be utilised as an in vitro model system to examine the modulation of xenobiotic-induced genotoxicity by flavonoids and other dietary components. (C) 1999 Elsevier Science B.V. AU rights reserved.
引用
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页码:91 / 100
页数:10
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