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生川乌瓜蒌不同配伍中乌头类生物碱在大鼠体内的药动学研究
引用本文:许妍妍,郭雪君,李遇伯,张艳军.生川乌瓜蒌不同配伍中乌头类生物碱在大鼠体内的药动学研究[J].现代药物与临床,2016,31(3):273-279.
作者姓名:许妍妍  郭雪君  李遇伯  张艳军
作者单位:1. 天津中医药大学中药学院,天津,300193;2. 天津市省部共建现代中药重点实验室,天津,300193
基金项目:国家重点基础研究发展计划项目(2011CB505300,2011CB505302);天津市高等学校科技发展基金计划项目(20140208)
摘    要:目的考察生川乌瓜蒌不同配伍比例醇提液中乌头类生物碱在大鼠体内的药动学研究,比较瓜蒌对其药动学行为的影响。方法建立灵敏、专属、快速的测定大鼠血浆中6种乌头类生物碱的液相色谱-串联质谱方法。大鼠随机分为3组,分别ig生川乌与瓜蒌1∶0、6∶1、1∶6配伍醇提液,在不同的时间点采血分析,经DAS 2.0软件计算主要药动学参数。结果乌头碱、次乌头碱、新乌头碱的药动学参数tmax和t1/2发生了显著变化,且变化趋势基本一致,在生川乌与瓜蒌6∶1配伍组tmax显著减小(P0.05),生川乌与瓜蒌1∶6配伍组tmax显著增加(P0.01、0.001),且t_(1/2)显著降低(P0.05、0.01),提示生川乌与瓜蒌不同配伍比例影响了3种生物碱的吸收和消除过程。结论生川乌与瓜蒌配伍影响了乌头类生物碱的药动学过程,配伍比例是其配伍禁忌的重要条件。

关 键 词:生川乌  瓜蒌  配伍  药动学  LC-MS/MS
收稿时间:2016/1/25 0:00:00

Pharmacokinetic studies on aconitum alkaloids from Aconiti Radix in different compatibility with Trichosanthis Fructus in rats
XU Yan-yan,GUO Xue-jun,LI Yu-bo and ZHANG Yan-jun.Pharmacokinetic studies on aconitum alkaloids from Aconiti Radix in different compatibility with Trichosanthis Fructus in rats[J].Drugs & Clinic,2016,31(3):273-279.
Authors:XU Yan-yan  GUO Xue-jun  LI Yu-bo and ZHANG Yan-jun
Institution:College of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China;College of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China;College of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China;Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China
Abstract:Objective To study pharmacokinetics of aconitum alkaloids from ethanol extracts of Aconiti Radix and Trichosanthis Fructus in different compatibility ratios after oral administration to rats, and compare the influence of Trichosanthis Fructus on pharmacokinetic characterization of Aconiti Radix. Methods A sensitive, selective and rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was established for simultaneous determination of the six aconitum alkaloids in rat plasma. Rats were randomly divided to three groups, and were given ethanol extracts of Aconiti Radix and Trichosanthis Fructus in different compatibility ratios (1:0, 6:1 and 1:6), respectively. Blood samples were withdrawn at different time points and analyzed. Main pharmacokinetic parameters were calculated using DAS 2.0 Software Package. Results Pharmacokinetic parameters including tmax and t1/2 of aconitine, hypaconitine, and mesaconitine varied significantly after compatibility, with almost the same variation trend. Compared with Aconiti Radix group, tmax of aconitine, hypaconitine, and mesaconitine decreased significantly (P < 0.05) in group of Aconiti Radix and Trichosanthis Fructus in compatibility ratio of 6:1, while increased significantly (P < 0.01, 0.001) in group of Aconiti Radix and Trichosanthis Fructus in compatibility ratio of 1:6. T1/2 of aconitine, hypaconitine, and mesaconitine decreased significantly (P < 0.05, 0.01) in group of Aconiti Radix and Trichosanthis Fructus in compatibility ratio of 1:6. The compatibility of Aconiti Radix and Trichosanthis Fructus could affect absorption and elimination of the three aconitum alkaloids. Conclusion Aconiti Radix in compatibility with Trichosanthis Fructus led to pharmacokinetic alteration of the aconitum alkaloids, and compatibility ratio is an important condition for the incompatibility of Aconiti Radix and Trichosanthis Fructus.
Keywords:Aconiti Radix  Trichosanthis Fructus  compatibility  pharmacokinetics  LC-MS/MS
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