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王爱国, 邓淑凯, 夏涛, 袁晶, 余日安, 陈学敏, 杨克敌. 苯巴比妥对双氯芬酸钠毒性和代谢的影响[J]. 中国公共卫生, 2004, 20(6): 662-663.
引用本文: 王爱国, 邓淑凯, 夏涛, 袁晶, 余日安, 陈学敏, 杨克敌. 苯巴比妥对双氯芬酸钠毒性和代谢的影响[J]. 中国公共卫生, 2004, 20(6): 662-663.
WANG Ai-guo, DENG Shu-kai, XIA Tao, . Effect of phenobarbital on metabolism and toxicity of diclofenac sodium in vitro[J]. Chinese Journal of Public Health, 2004, 20(6): 662-663.
Citation: WANG Ai-guo, DENG Shu-kai, XIA Tao, . Effect of phenobarbital on metabolism and toxicity of diclofenac sodium in vitro[J]. Chinese Journal of Public Health, 2004, 20(6): 662-663.

苯巴比妥对双氯芬酸钠毒性和代谢的影响

Effect of phenobarbital on metabolism and toxicity of diclofenac sodium in vitro

  • 摘要:
      目的   研究苯巴比妥对双氯芬酸钠毒性和代谢的影响。
      方法   用夹层细胞培养的方法, 将双氯芬酸钠暴露于大鼠肝细胞或经苯巴比妥预处理后的肝细胞, 测定培养液中肝细胞酶渗出量、细胞色素P4503A(CYP3A)活性和双氯芬酸钠代谢产物的含量。
      结果   肝细胞基础CYP3A活性随培养时间的延长而逐渐降低, CYP3A的这种下降趋势可被细胞色素P450诱导剂如苯巴比妥所改变。培养液中乳酸脱氢酶(LDH), 丙氨酸转氨酶(ADLT)和天冬氨酸转氨酶(AST)水平及双氯芬酸钠代谢产物4'-OH-DF和5-OH-DF的含量随双氯芬酸钠暴露浓度的增加而增加, 各暴露组之间以及暴露组与对照组之间未见显著性差异。但肝细胞经苯巴比妥预处理后, 再暴露于双氯芬酸钠中, 培养液中4'-OH-DF和5-OH-DF浓度以及LDH水平均明显增加。
      结论   随着肝细胞内CYP3A活性的增强, 双氯芬酸钠对肝细胞的毒性和在肝细胞中的代谢都会增强。

     

    Abstract:
      Objective   To investigate the effects of phenobarbital (PB) on metabolism and toxicity of diclofenac sodium (DF-Na) in vitro.
      Methods   Rathepatocytes were isolated and cultured with sandwich method.The enzyme leakage level, cytochrome P4503A(CYP3A)activity, and metabolite content of DF-Na in cell culture medium were measured after hepatocytes or PB pre-treated hepatocytes were incubated with DF-Na in vitro.
      Results   Basic hepatic CYP3A activity grad-ually decreased with culture time.The decline of CYP3A was partially reversed by using cytochrome P450 inducer such as PB.The activities of lactic dehydrogenase(LDH), alanine transminase(ALT), and aspartate transminase(AST)and the contents of metabolite 4'-hydroxydiclofenac(4'-OH-DF)and 5-hydroxydiclofenac(5-OH-DF)in superatants were found to increase with the DF-Na exposure concentrations.But there were no significant difference between exposed group and control group.However, if the hepatocytes first were pre-treated with PB and then exposed to DF-Na, the concentrations of DF-Na metabolites and the activity of LDH in the supernatants were significantly higher than that of control group.
      Conclusion   The hepatotoxicity and metabolism of DF-Na in rathepatocytes should be increased when CYP3A activity increased.

     

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