Gawrońska-Szklarz B, Drozdzik M, Wójcicki J, Zakrzewski J
Department of Clinical Pharmacology, School of Medicine, Szczecin, Poland.
Acta Pol Pharm. 1994;51(3):271-4.
The study was carried out on 18 male rabbits randomaly ascribed into two groups: control one on standard diet and experimental one on high-fat diet for 2 months. Pharmacokinetic assays were performed in all animals after 2 months of the experiment. Blood was sampled within 24 hours after intragastrical administration of digoxin at a dose 0.02 mg/kg. The two compartment open model for extravascular administration was used for calculations. Marked increase in plasma drug concentration, as well as decrease in total clearance were noted. The study revealed the influence of experimental hyperlipidemia on digoxin pharmacokinetics leading to a slower drug elimination.
该研究对18只雄性兔子进行,随机分为两组:对照组给予标准饮食,实验组给予高脂饮食,持续2个月。实验2个月后对所有动物进行药代动力学测定。在以0.02 mg/kg的剂量经胃内给予地高辛后24小时内采集血液样本。采用血管外给药的二室开放模型进行计算。结果发现血浆药物浓度显著升高,总清除率降低。该研究揭示了实验性高脂血症对地高辛药代动力学的影响,导致药物消除减慢。