Kovalev I E, Kovalev E N, Seleznev N G, Kuvshinova R L
Zh Nevropatol Psikhiatr Im S S Korsakova. 1984;84(2):198-201.
Metabolic activity of the mononuclear phagocytic system (MPS) was studied in 65 patients with disseminated sclerosis (DS) and 65 control persons by determination of the test-substance biotransformation intensity. Sulfadimezine undergoing acetylation in MPS cells was chosen as a test-substance. Sulfadimezine was administered per os; both unchanged drug and its acetylated metabolite were detected in urine in 6 hours. Correlation between acetylated and non-acetylated sulfadimezine levels permitted dividing the examinees into "rapid" or "slow" acetylators (inactivators). Patients with DS belong mainly to slow acetylators since the test-substance in MPS cells of these patients is inactivated slowly. Correlation between "slow" and "rapid" acetylators in patients with DS was 5:1, that in the control group 2:1. A similar pattern was reported previously in patient with systemic lupus erythematosus. New approaches to the mechanisms of DS development based on MPS functions analysis are outlined.
通过测定受试物质的生物转化强度,对65例播散性硬化症(DS)患者和65名对照者的单核吞噬细胞系统(MPS)的代谢活性进行了研究。选用在MPS细胞中发生乙酰化的磺胺二甲嘧啶作为受试物质。磺胺二甲嘧啶经口服给药;6小时后在尿液中检测到未改变的药物及其乙酰化代谢产物。根据乙酰化和未乙酰化磺胺二甲嘧啶水平之间的相关性,可将受试者分为“快速”或“慢速”乙酰化者(失活者)。DS患者主要属于慢速乙酰化者,因为这些患者MPS细胞中的受试物质失活缓慢。DS患者中“慢速”和“快速”乙酰化者的比例为5:1,对照组为2:1。先前在系统性红斑狼疮患者中也报道过类似模式。概述了基于MPS功能分析的DS发病机制的新方法。