Kobayashi S, Tanaka E, Oguchi K, Yoshida T, Kuroiwa Y, Yasuhara H
J Pharmacobiodyn. 1984 May;7(5):329-35. doi: 10.1248/bpb1978.7.329.
There have been significant correlations between serum concentration ratios of 5,5-dimethyl-2,4-oxazolidinedione (Dimethadione, DMO)/trimethadione (TMO) after administration of TMO and hepatic microsomal cytochrome P-450 contents in rats with various treatments (CCl4 or phenobarbital). The pharmacokinetics of TMO and DMO, and the serum concentration ratio of DMO/TMO have been investigated in healthy volunteers after oral administration of 1 mg/kg (N = 4), 2 mg/kg (N = 6) and 4 mg/kg (N = 6) TMO, respectively. TMO and DMO concentrations in serum were determined by a gas-liquid chromatographic method. Serum disappearance of TMO was described by one compartment model. The T1/2, Kel, Vd and C1 of TMO and of DMO were shown to have almost the same values in 2 mg/kg or 4 mg/kg TMO administration. Correlation coefficient between DMO/TMO ratio in serum and time course after 1 mg/kg, 2 mg/kg and 4 mg/kg TMO administration was found to be r = 0.958, r = 0.924 and r = 0.938, respectively. These results indicate that the serum concentration ratio of DMO/TMO, especially at 2 or 4 h after 4 mg/kg TMO administration orally, may be an index of hepatic drug-metabolizing capacity in human serum as well as in rats.
给予不同处理(四氯化碳或苯巴比妥)的大鼠服用三甲双酮(TMO)后,其血清中5,5 - 二甲基 - 2,4 - 恶唑烷二酮(二甲双酮,DMO)/三甲双酮(TMO)的浓度比与肝微粒体细胞色素P - 450含量之间存在显著相关性。分别对健康志愿者口服1mg/kg(N = 4)、2mg/kg(N = 6)和4mg/kg(N = 6)的TMO后,研究了TMO和DMO的药代动力学以及DMO/TMO的血清浓度比。采用气液色谱法测定血清中TMO和DMO的浓度。TMO的血清消除情况用一室模型描述。在给予2mg/kg或4mg/kg TMO时,TMO和DMO的T1/2、Kel、Vd和C1显示出几乎相同的值。在口服1mg/kg、2mg/kg和4mg/kg TMO后,血清中DMO/TMO比值与时间进程之间的相关系数分别为r = 0.958、r = 0.924和r = 0.938。这些结果表明,DMO/TMO的血清浓度比,尤其是在口服4mg/kg TMO后2或4小时,可能是人血清以及大鼠肝脏药物代谢能力的一个指标。