Uetrecht J P, Freeman R W, Woosley R L
Arthritis Rheum. 1981 Aug;24(8):994-1003. doi: 10.1002/art.1780240803.
The principal metabolic pathway of procainamide leads to formation of the less toxic N-acetyl-procainamide and the rapid acetylator phenotype is associated with a lower incidence of procainamide-induced lupus. Another metabolic pathway forms a reactive metabolite which causes revertants in the Ames test and covalently binds to microsomal protein. A study of the metabolism of procainamide revealed three metabolites that have not been previously described. A comparison of the metabolites of N-acetylprocainamide with those of procainamide suggests possibilities for the identity of the reactive metabolite. The hypotheses to be discussed explore the relationships between the formation of a reactive metabolite and the induction of lupus.
普鲁卡因胺的主要代谢途径会导致生成毒性较低的N - 乙酰普鲁卡因胺,快速乙酰化表型与普鲁卡因胺诱导的狼疮发生率较低相关。另一条代谢途径会形成一种反应性代谢产物,该产物在艾姆斯试验中会导致回复突变,并与微粒体蛋白共价结合。一项关于普鲁卡因胺代谢的研究揭示了三种先前未被描述的代谢产物。将N - 乙酰普鲁卡因胺的代谢产物与普鲁卡因胺的代谢产物进行比较,为反应性代谢产物的身份提供了一些可能性。即将讨论的假设探讨了反应性代谢产物的形成与狼疮诱导之间的关系。