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中国临床药理学与治疗学 ›› 2011, Vol. 16 ›› Issue (5): 545-548.

• 临床药理学 • 上一篇    下一篇

天然维生素E对P-糖蛋白活性影响的体内研究

张松波1,2, 段娟3, 周宏灏2   

  1. 1岳阳职业技术学院,岳阳 414000,湖南;
    2中南大学临床药理研究所,长沙 410078,湖南;
    3湖南省血防所附属医院,岳阳 414000,湖南
  • 收稿日期:2011-04-01 修回日期:2011-04-15 发布日期:2011-07-08
  • 作者简介:张松波,男,药理学硕士,讲师,研究方向:药物基因组学及临床药理。Tel:13973067097 E-mail:zsb8283271@163.com周宏灏,教授,中国工程院院士,研究方向:遗传药理学与药物基因组学。Tel:0731-4805380 E-mail:hhzhou2003@163.com

Effects of regular consumption of RRR-α-tocopherol on the activity of P-gp in vivo

ZHANG Song-bo1,2, DUAN Juan3, ZHOU Hong-hao2   

  1. 1Yueyang Vocational Technical College, Yueyang 414000, Hunan, China;
    2The Institute of Clinical Pharmacology, Central South University, Changsha 410078, Hunan, China;
    3Affiliated Xiangyue Hospital, Hunan Provincial Dispensary of Schistosomiasis, Yueyang 414000, Hunan, China
  • Received:2011-04-01 Revised:2011-04-15 Published:2011-07-08

摘要: 目的: 阐明天然维生素E在体内对P-糖蛋白活性的影响。方法: 12名健康志愿者,随机分两组,采用两阶段双周期交叉设计,一组口服天然维生素E 600 mg/d,另一组不服药,连续 14 d,在第15天两组均口服他林洛尔 100 mg,在0、0.25、0.5、0.75、1、1.5、2、2.5、3、4、6、8、12、24 h 采外周静脉血 5 mL,洗脱4周交叉进行下阶段实验。采血后 0.5 h 内进行离心和分离血浆,运用HPLC测定他林洛尔血浆中药物浓度,分析比较不同服药组间药代动力学参数的差异。结果: 天然维生素E明显降低了他林洛尔的血药浓度。天然维生素E服用组与对照组之间他林洛尔曲线下面积AUC(0-24 h)分别为(2104±670)和(2914±1061) ng·h·mL-1,P<0.05;峰浓度Cmax分别为(249±69) ng/mL和(406±214) ng/mL,P<0.05。结论: 口服天然维生素E 600 mg,连续 14 d,明显诱导了P-糖蛋白的活性。

关键词: 天然维生素E, 他林洛尔, 孕烷X受体, P-糖蛋白

Abstract: AIM: To investigate the effect of regular consumption of RRR-α-tocopherol on the activity of P-gp in vivo.METHODS: In a two-stage doubly periodic cross-over study, 12 healthy volunteers, who were randomly divided into two groups, ingested RRR-α-tocopherol 600 mg each day or placebo (control) for 14 d. On day 15, a single 100 mg dose of talinolol was administered by all the volunteers and 5 mL peripheral vein blood of each one was taken at 0, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24 h. Plasma concentrations of talinolol were determined by HPLC after centrifugation and blood plasma separation. The difference of pharmacokinetic parameters of every groups were compared and analyzed.RESULTS: Co-administration of RRR-α-tocopherol obviously decreased the area under the curve AUC(0-24h) of talinolol [(2104±670) ng·h·mL-1 vs (2914±1061) ng·h·mL-1], P<0.05, and significantly decreased Cmax of talinolol [(249±69) ng/mL vs (406±214) ng/mL], P<0.05.CONCLUSION: Regular consumption of RRR-α-tocopherol 600 mg each day for 14 d, significantly induces the activity of P-gp.

Key words: RRR-α-tocopherol, Talinolol, PXR, P-gp

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