Maines M D
Crit Rev Toxicol. 1984;12(3):241-314. doi: 10.3109/10408448409021604.
Various endogenous and exogenous chemicals, such as hormones, drugs, and carcinogens and other environmental pollutants are enzymatically converted to polar metabolites as a result of their oxidative metabolism by the mixed-function oxidase system. This enzyme complex constitutes the major detoxifying system of man and utilizes the hemoprotein--cytochrome P-450--as the terminal oxidase. Recent studies with trace metals have revealed the potent ability of these elements to alter the synthesis and to enhance the degradation of heme moiety of cytochrome P-450. An important consequence of these metal actions is to greatly impair the ability of cells to oxidatively metabolize chemicals because of the heme dependence of this metabolic process. In this report the effects of exposure to trace metals on drug oxidations is reviewed within the framework of metal alterations of heme metabolism, including both its synthesis and degradation, since these newly discovered properties of metals have made it possible to define a major dimension of metal toxicity in terms of a unified cellular mechanism of action.
各种内源性和外源性化学物质,如激素、药物、致癌物及其他环境污染物,通过混合功能氧化酶系统的氧化代谢作用,被酶促转化为极性代谢产物。该酶复合物构成了人体主要的解毒系统,并利用血红素蛋白——细胞色素P - 450——作为末端氧化酶。近期对痕量金属的研究表明,这些元素具有改变细胞色素P - 450血红素部分合成并增强其降解的强大能力。这些金属作用的一个重要后果是,由于该代谢过程对血红素的依赖性,极大地损害了细胞氧化代谢化学物质的能力。在本报告中,鉴于痕量金属对血红素代谢(包括其合成和降解)的影响,对接触痕量金属对药物氧化的影响进行了综述,因为这些新发现的金属特性使得从统一的细胞作用机制角度定义金属毒性的一个主要方面成为可能。