Xu Mei-Juan, Wang Guang-Ji, Xie Hai-Tang, Li Hao, Huang Qing, Wang Rui, Jia Yuan-Wei, Lv Tian
Key Laboratory of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing, Jiangsu, Peoples Republic of China.
Eur J Drug Metab Pharmacokinet. 2008 Apr-Jun;33(2):65-8. doi: 10.1007/BF03191022.
The difference in the pharmacokinetics of schizandrin (SZ) in male and female rats was studied. SZ concentrations in the plasma were determined after the intragastric (i.g) administration of 10 mg/kg and the intravenous (i.v) administration of 5 mg/kg in male and female rats, respectively. It was found that the plasma concentrations of SZ in female rats were significantly higher than those in male rats. Drug absolute bioavailability, based on the area under curve (AUC(0-tn)), in female rats was roughly 20 times of that in male rats. The terminate half-life (T(1/2)) in male rats was shorter than that in female rats. These results demonstrate the existence of marked gender differences for SZ in rats.
研究了五味子醇甲(SZ)在雄性和雌性大鼠体内的药代动力学差异。分别对雄性和雌性大鼠进行10mg/kg灌胃给药和5mg/kg静脉给药后,测定血浆中SZ的浓度。结果发现,雌性大鼠血浆中SZ的浓度显著高于雄性大鼠。基于曲线下面积(AUC(0-tn))计算的药物绝对生物利用度,雌性大鼠约为雄性大鼠的20倍。雄性大鼠的消除半衰期(T(1/2))短于雌性大鼠。这些结果表明,大鼠体内SZ存在明显的性别差异。