Koop D R, Tierney D J
Department of Environmental Health Sciences, Case Western Reserve University, School of Medicine, Cleveland, OH 44106.
Bioessays. 1990 Sep;12(9):429-35. doi: 10.1002/bies.950120906.
Cytochrome P450IIE1 is involved in the metabolic activation of many xenobiotics involved with human toxicity. In particular, cellular concentrations of P450IIE1 are significantly induced by the most widely abused drug in our society today, alcohol. As a result, the synthesis and degradation of this form of P450 has significant health consequences. The regulation of the steady-state concentration of P450IIE1 is an extremely complex process. The enzyme is regulated by transcriptional activation, mRNA stabilization, increased mRNA translatability and decreased protein degradation. The principal mechanism which controls the induction process depends on the chemical nature of the inducer, the age, and the nutritional and hormonal status of the animal. There also appear to be significant sex differences in the expression of P450IIE1. It is entirely possible that the regulation of the enzyme concentration under any given set of conditions will involve all of the mechanisms to different extents.
细胞色素P450IIE1参与许多与人类毒性相关的外源性物质的代谢活化。特别是,当今社会最广泛滥用的药物酒精可显著诱导细胞中P450IIE1的浓度。因此,这种形式的P450的合成和降解具有重大的健康影响。P450IIE1稳态浓度的调节是一个极其复杂的过程。该酶受转录激活、mRNA稳定、mRNA可翻译性增加和蛋白质降解减少的调节。控制诱导过程的主要机制取决于诱导剂的化学性质、动物的年龄以及营养和激素状态。P450IIE1的表达似乎也存在显著的性别差异。在任何给定条件下,酶浓度的调节完全有可能在不同程度上涉及所有这些机制。