Key Laboratory of Modern Preparation of TCM, Ministry of Education, Jiangxi University of TCM, No.18 Yun Wan Road, Nanchang 330004, PR China.
J Ethnopharmacol. 2013 Jan 9;145(1):77-84. doi: 10.1016/j.jep.2012.09.054. Epub 2012 Nov 1.
Fritillaria thunbergii Miq. has been traditionally used in China as antitussive and expectorant herbs, and newly used in the clinical treatment of leukemia in recent years.
To investigate whether gender exerted a significant influence on the pharmacokinetics, tissue distribution and excretion of peimine and peiminine in Sprague-Dawley rats who were given a single oral administration of 4.25 g/kg Fritillaria thunbergii Miq. extract.
Sprague-Dawley rats were assigned into two groups based on the gender and orally administered 4.25 g/kg Fritillaria thunbergii Miq. extract for each individual pharmacokinetics, tissue distribution and excretion study.
Compared with female rats, peimine and peiminine were eliminated slowly from male rat plasma, and significant gender-related differences were observed in the pharmacokinetic parameters. Drug blood and tissue levels in male rats were significantly higher than the female counterparts except for several tissues, such as fat, muscle and skin. Gender also exerted a significant influence on the urine excretion but such effect was not observed in the feces excretion study.
Gender exerted a significant influence on the pharmacokinetics, tissue distribution and urine excretion of peimine and peiminine. It is assumed that the sex-associated differences of peimine and peiminine in rats might be mainly result from sex-dependent expression and activity of drug metabolism enzymes and P-glycoprotein.
浙贝母在传统上被用作镇咳和祛痰草药,近年来也被新应用于白血病的临床治疗。
研究性别是否对给予 4.25 g/kg 浙贝母提取物的雄性和雌性 Sprague-Dawley 大鼠单次口服后的贝母甲素和贝母乙素的药代动力学、组织分布和排泄产生显著影响。
根据性别将 Sprague-Dawley 大鼠分为两组,并对每组进行单独的药代动力学、组织分布和排泄研究。
与雌性大鼠相比,雄性大鼠血浆中的贝母甲素和贝母乙素消除缓慢,药代动力学参数存在显著的性别相关性差异。除脂肪、肌肉和皮肤等几种组织外,雄性大鼠的药物血和组织水平明显高于雌性大鼠。性别对尿液排泄也有显著影响,但在粪便排泄研究中未观察到这种影响。
性别对贝母甲素和贝母乙素的药代动力学、组织分布和尿液排泄有显著影响。据推测,大鼠中贝母甲素和贝母乙素的性别相关差异主要是由于药物代谢酶和 P-糖蛋白的性别依赖性表达和活性所致。