Matsuura Y, Fukuda T, Yoshida T, Kuroiwa Y
Department of Hygienic Chemistry, Showa College of Pharmaceutical Sciences, Tokyo, Japan.
Toxicology. 1988 Jul;50(2):169-80. doi: 10.1016/0300-483x(88)90089-3.
Pretreatment of rats with zinc-protoporphyrin, which has shown to be a potent competitive inhibitor of heme oxygenase, resulted in the inhibition of bromobenzene-mediated induction of heme oxygenase and decreases of the cytochrome P-450 content, aminopyrine demethylase and aniline hydroxylase activities. Such an inhibitory effect of zinc-protoporphyrin on the induction of heme oxygenase and concomitant decreases of drug-metabolizing enzymes occurred in a dose-dependent manner with complete inhibition of these effects at a dose of 40 mumol/kg. The effects of zinc-protoporphyrin were also observed in thioacetamide- and BCG-treated rats and ascitic tumor AH 66-bearing rats. Likewise, a decrease of cytochrome b5 content observed under these experimental conditions was also restored significantly by zinc-protoporphyrin. These results strongly suggest that the induction of heme oxygenase is a primarily important early event which consequently leads to the decrease in cytochrome P-450 content and associated enzyme activities.
用锌原卟啉预处理大鼠,已证明锌原卟啉是血红素加氧酶的一种有效竞争性抑制剂,这导致了溴苯介导的血红素加氧酶诱导作用受到抑制,细胞色素P - 450含量、氨基比林脱甲基酶和苯胺羟化酶活性降低。锌原卟啉对血红素加氧酶诱导作用的这种抑制效应以及药物代谢酶的相应降低呈剂量依赖性,在剂量为40 μmol/kg时这些效应完全被抑制。在硫代乙酰胺和卡介苗处理的大鼠以及荷腹水瘤AH 66的大鼠中也观察到了锌原卟啉的作用。同样,在这些实验条件下观察到的细胞色素b5含量降低也被锌原卟啉显著恢复。这些结果有力地表明,血红素加氧酶的诱导是一个至关重要的早期事件,其结果是导致细胞色素P - 450含量及相关酶活性降低。