The effects of benzimidazole anthelmintics on P4501A in rat hepatocytes and HepG2 cells

被引:24
作者
Baliharová, V
Skálová, L
Maas, RFM
De Vrieze, G
Bull, S
Fink-Gremmels, J
机构
[1] Charles Univ, Fac Pharm, CZ-50005 Hradec Kralove, Czech Republic
[2] Univ Utrecht, Fac Vet Med, NL-3508 TD Utrecht, Netherlands
关键词
benzimidazole anthelmintics; cytochromes P4501A; rat hepatocytes; HepG2; cells; enzyme induction;
D O I
10.1016/S0034-5288(03)00033-X
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Benzimidazole anthelmintics including albendazole, fenbendazole, and mebendazole are widely used in veterinary medicine. The effects of these benzimidazoles on cytochrome P4501A were investigated in primary cultures of rat hepatocytes and in the HepG2 cell line. After incubation of rat hepatocytes and HepG2 for 24-, 48-, and 72-h cells with drugs at various concentrations (0.1-50muM), the enzyme activities associated with P4501A1/2 (7-ethoxyresorufin O-deethylation and 7-methoxyresorufin O-demethylation) were measured. The P4501A1/2 protein levels in both model systems were determined by Western blotting. Although all benzimidazoles provoked a significant increase of P4501A1/2 protein levels and P4501A activities, large differences in the induction response were found which was dependent on drug structure, concentration, and model system used. Based on the results, relationships between induction potency and structure of drug were demonstrated, as well as differences between the in vitro systems used. Therefore, pharmacological and toxicological consequences of cytochrome P4501A induction by benzimidazole drugs should be taken into account in veterinary therapy. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:61 / 69
页数:9
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