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舒普拉他及其代谢产物对大鼠茶碱代谢的抑制作用。

Inhibition of theophylline metabolism by suplatast and its metabolites in rats.

作者信息

Kizawa Makiko, Miyamoto Etsuko, Aono Shuka, Kawakami Junichi, Adachi Isao

机构信息

Department of Hospital Pharmacy, Toyama Medical and Pharmaceutical University, Japan.

出版信息

Biol Pharm Bull. 2005 Jun;28(6):1061-5. doi: 10.1248/bpb.28.1061.

Abstract

The inhibitory effect of suplatast (ST), an anti-allergic drug, on theophylline (TP) metabolism was investigated in rats in vivo and in vitro. Intravenous injection of aminophylline (AP) at 10 mg/kg of TP equivalent was performed with or without pretreatment by oral administration of 100 mg/kg of ST 2.5 h prior to AP. In the ST-pretreated group, plasma concentration (Cp), the area under Cp-time profile (AUC) and urinary excretion of TP increased significantly, and urinary excretion of TP metabolites, 1,3-dimethyluric acid (DMU) and 1-methyluric acid (1MU) decreased significantly. Metabolic clearance of DMU (CL(DMU)) and that of 1MU (CL(1MU)) were remarkably suppressed by ST pretreatment, however, renal clearance (CLr) of TP did not change. To compare the inhibitory effect of ST on TP metabolism with that of its main metabolite (M1) in vivo, a concomitant intravenous injection of AP (10 mg/kg of TP equivalent) with ST or M1 (40 mg/kg of ST equivalent) was carried out. In the M1 group, Cp and AUC of TP increased significantly, and the total body clearance of TP decreased significantly. In contrast, ST did not induce these changes. Then, the inhibitory effect of ST and M1 on TP metabolism in vitro was evaluated using rat-liver microsomes. ST and M1 suppressed DMU formation in a competitively inhibitory manner, and their equilibrium dissociation constants (Ki) were 822 and 731 microM, respectively. In conclusion, inhibition of TP metabolism by ST was demonstrated in vivo and in vitro, and the involvement of M1 and/or other metabolites in this drug interaction was suggested.

摘要

在大鼠体内和体外研究了抗过敏药物色甘酸钠(ST)对茶碱(TP)代谢的抑制作用。以10mg/kg的TP等效剂量静脉注射氨茶碱(AP),在注射AP前2.5小时,分别给予或不给予100mg/kg的ST口服预处理。在ST预处理组中,TP的血浆浓度(Cp)、Cp-时间曲线下面积(AUC)和尿排泄量显著增加,而TP代谢产物1,3-二甲基尿酸(DMU)和1-甲基尿酸(1MU)的尿排泄量显著减少。ST预处理显著抑制了DMU的代谢清除率(CL(DMU))和1MU的代谢清除率(CL(1MU)),然而,TP的肾清除率(CLr)没有变化。为了在体内比较ST与其主要代谢产物(M1)对TP代谢的抑制作用,同时静脉注射AP(10mg/kg的TP等效剂量)与ST或M1(40mg/kg的ST等效剂量)。在M1组中,TP的Cp和AUC显著增加,TP的总体清除率显著降低。相比之下,ST没有引起这些变化。然后,使用大鼠肝微粒体评估ST和M1在体外对TP代谢的抑制作用。ST和M1以竞争性抑制方式抑制DMU的形成,它们的平衡解离常数(Ki)分别为822和731μM。总之,在体内和体外均证明了ST对TP代谢的抑制作用,并提示M1和/或其他代谢产物参与了这种药物相互作用。

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