Jacobsen D, Barron S K, Sebastian C S, Blomstrand R, McMartin K E
Department of Pharmacology and Therapeutics, Louisiana State University Medical Center, Shreveport.
Eur J Clin Pharmacol. 1989;37(6):599-604. doi: 10.1007/BF00562552.
In order to evaluate the pharmacokinetic profile of the alcohol dehydrogenase inhibitor 4-methylpyrazole 4-MP, a placebo-controlled, double-blind, single-dose, randomized, sequential, ascending-dose "Phase-I study" was performed in healthy male volunteers at dose levels of 10 (n = 4), 20 (n = 4), 50 (n = 4) and 100 mg.kg-1 (n = 3). In the 10 and 20 mg.kg-1 group, the elimination of 4-MP from the plasma followed non-linear kinetics with mean rates of concentration decline of 3.66 and 5.05 mumol.l-1.h-1, respectively. In the two highest dose groups, the elimination also appeared to be non-linear although the patterns were not followed long enough to confirm this. The mean rates of concentration decline at the higher doses were significantly increased, up to 14.9 mumol.l-1.h-1 at 100 mg.kg-1. The average renal clearance of 4-MP was low, 0.016 ml.min-1.kg-1, and only 3% of the administered dose was excreted unchanged in the urine, indicating metabolism as the major route of elimination. Because of the apparently unusual kinetics following single dose treatment, thorough multiple dose studies need to be carried out to determine a safe dosage regimen for 4-MP.
为评估乙醇脱氢酶抑制剂4-甲基吡唑(4-MP)的药代动力学特征,在健康男性志愿者中进行了一项安慰剂对照、双盲、单剂量、随机、序贯、递增剂量的“Ⅰ期研究”,剂量水平分别为10(n = 4)、20(n = 4)、50(n = 4)和100 mg·kg⁻¹(n = 3)。在10和20 mg·kg⁻¹组中,4-MP从血浆中的消除遵循非线性动力学,平均浓度下降速率分别为3.66和5.05 μmol·L⁻¹·h⁻¹。在两个最高剂量组中,消除似乎也是非线性的,尽管观察时间不够长,无法证实这一点。较高剂量下的平均浓度下降速率显著增加,在100 mg·kg⁻¹时高达14.9 μmol·L⁻¹·h⁻¹。4-MP的平均肾清除率较低,为0.016 ml·min⁻¹·kg⁻¹,仅3%的给药剂量以原形从尿液中排泄,表明代谢是主要的消除途径。由于单次给药后动力学表现异常,需要进行全面的多次给药研究,以确定4-MP的安全给药方案。