Ohashi K, Sudo T, Sakamoto K, Tateishi T, Fujimura A, Kumagai Y, Shiga T, Ebihara A
Department of Clinical Pharmacology, Jichi Medical School, Tochigi, Japan.
Int J Clin Pharmacol Ther Toxicol. 1992 Aug;30(8):271-4.
The effect of diltiazem pretreatment on the pharmacokinetics and pharmacodynamics of MPC-1304, a new calcium channel blocker, were evaluated in six healthy male volunteers. Placebo or diltiazem 60 mg was given orally three times daily for 3 days in a double-blind crossover method. MPC-1304 10 mg was administered orally two times at an interval of four weeks as a washout period. Diltiazem significantly increased the maximum plasma level (Cmax) and the area under the plasma concentration-time curve (AUC) of MPC-1304 from control values (3.0 +/- 1.5 to 10.2 +/- 4.8 ng/ml, p less than 0.05, and 11.0 +/- 3.8 to 36.0 +/- 15.6 ng.h/ml, p less than 0.01, respectively) without any changes of t1/2. In the case of the major active metabolite, side chain reduced form (MI), Cmax, AUC, and t1/2 were significantly increased by diltiazem as follows: Cmax, 60.7 +/- 21.1 to 171.4 +/- 73.6 ng/ml, p less than 0.05; AUC, 317.6 +/- 62.6 to 1,334.9 +/- 563.6 ng.h/ml, p less than 0.01; t1/2, 2.8 +/- 0.7 to 3.9 +/- 0.6 h, p less than 0.01. Diltiazem pretreatment slightly, but not significantly decreased blood pressure after MPC-1304 dosing. The inhibition of hepatic metabolism on MPC-1304 may explain the significant changes in pharmacokinetics of MPC-1304 after diltiazem pretreatment.
在六名健康男性志愿者中评估了地尔硫䓬预处理对新型钙通道阻滞剂MPC - 1304药代动力学和药效学的影响。采用双盲交叉法,每日口服安慰剂或60毫克地尔硫䓬,共3天。在为期四周的洗脱期后,间隔四周口服两次10毫克MPC - 1304。地尔硫䓬使MPC - 1304的最大血浆浓度(Cmax)和血浆浓度 - 时间曲线下面积(AUC)较对照值显著增加(分别从3.0±1.5增至10.2±4.8纳克/毫升,p<0.05;从11.0±3.8增至36.0±15.6纳克·时/毫升,p<0.01),而t1/2无任何变化。对于主要活性代谢物,侧链还原形式(MI),地尔硫䓬使Cmax、AUC和t1/2显著增加,具体如下:Cmax,从60.7±21.1增至171.4±73.6纳克/毫升,p<0.05;AUC,从317.6±62.6增至1334.9±563.6纳克·时/毫升,p<0.01;t1/2,从2.8±0.7增至3.9±0.6小时,p<0.01。地尔硫䓬预处理在MPC - 1304给药后使血压略有下降,但不显著。地尔硫䓬预处理后对MPC - 1304肝脏代谢的抑制作用可能解释了MPC - 1304药代动力学的显著变化。