Waring R H
Department of Biochemistry, University of Birmingham, England.
Drug Metabol Drug Interact. 1988;6(3-4):253-63. doi: 10.1515/dmdi.1988.6.3-4.253.
The pharmacogenetics of S-carboxymethyl-L-cysteine (SCMC) have been studied in detail. When results from administration of SCMC to 200 volunteers were analysed, there was seen to be a wide interindividual variation in the percentage of sulphoxide metabolites excreted. Computer assisted analysis suggested that the population distribution observed could be most economically represented as two overlapping Gaussian distributions with the smaller mode representing poor sulphoxidisers. This phenomenon appears to be largely genetic in origin and to behave as though controlled by one autosomal recessive gene, but environmental factors may also be important. Poor sulphoxidisers seem to be overrepresented in certain patient populations with chronic diseases. These findings are discussed in terms of oxidative metabolism of sulphur-containing compounds.
已对S-羧甲基-L-半胱氨酸(SCMC)的药物遗传学进行了详细研究。在分析了给予200名志愿者SCMC后的结果后发现,所排泄的亚砜代谢物百分比存在很大的个体间差异。计算机辅助分析表明,观察到的总体分布最经济的表示方式是两个重叠的高斯分布,较小的众数代表亚砜氧化能力差的个体。这种现象似乎在很大程度上源于遗传,其表现就好像受一个常染色体隐性基因控制,但环境因素可能也很重要。在某些患有慢性疾病的患者群体中,亚砜氧化能力差的个体似乎占比过高。将根据含硫化合物的氧化代谢对这些发现进行讨论。