覃小玲, 段文海, 王海帆, 王莹, 陈孝, 黄民, 毕惠嫦. LC-MS/MS法测定五酯片中木脂素活性成分在大鼠肝脏及肠道的分布J. 药学学报, 2016,51(12): 1891-1896. doi: 10.16438/j.0513-4870.2016-0526
引用本文: 覃小玲, 段文海, 王海帆, 王莹, 陈孝, 黄民, 毕惠嫦. LC-MS/MS法测定五酯片中木脂素活性成分在大鼠肝脏及肠道的分布J. 药学学报, 2016,51(12): 1891-1896. doi: 10.16438/j.0513-4870.2016-0526
QIN Xiao-ling, DUAN Wen-hai, WANG Hai-fan, WANG Ying, CHEN Xiao, HUANG Min, BI Hui-chang. Determination of hepatic and small intestinal distribution of lignans of Wuzhi tablet in rats by liquid chromatography tandem mass spectrometry methodJ. Acta Pharmaceutica Sinica, 2016,51(12): 1891-1896. doi: 10.16438/j.0513-4870.2016-0526
Citation: QIN Xiao-ling, DUAN Wen-hai, WANG Hai-fan, WANG Ying, CHEN Xiao, HUANG Min, BI Hui-chang. Determination of hepatic and small intestinal distribution of lignans of Wuzhi tablet in rats by liquid chromatography tandem mass spectrometry methodJ. Acta Pharmaceutica Sinica, 2016,51(12): 1891-1896. doi: 10.16438/j.0513-4870.2016-0526

LC-MS/MS法测定五酯片中木脂素活性成分在大鼠肝脏及肠道的分布

Determination of hepatic and small intestinal distribution of lignans of Wuzhi tablet in rats by liquid chromatography tandem mass spectrometry method

  • 摘要: 本研究利用LC-MS/MS方法考察单次灌胃给予五酯片后其木脂素活性成分在大鼠肠道、肝脏的分布特点及随时间的变化规律。雄性SD大鼠灌胃给予五酯片0.25 g·kg-1后,于给药后0.25、1.5、4、6、10和24 h分批取大鼠肝脏及肠道组织,样本处理后进行LC-MS/MS分析。结果表明,五酯片各木脂素活性成分在大鼠肝脏、肠道的浓度随着五酯片给药时间的推移而降低;灌胃给予五酯片0.25 h后,五酯片各木脂素活性成分在大鼠肠道及肝脏中的浓度最高;灌胃给予五酯片24 h后,大鼠肠道及肝脏中检测不到五酯片各木脂素活性成分,提示五酯片各木脂素活性成分在脏器中消除较快,不容易蓄积。五味子酯甲、甲素、醇乙在肠道中的浓度高于其在肝脏中的浓度,提示灌胃给予五酯片可能对大鼠肠道、肝脏代谢酶作用强度存在差异。综上所述,单次灌胃给予五酯片,其木脂素活性成分不容易在大鼠肝脏及肠道蓄积,且大多数木脂素在肠道的浓度高于在肝脏的浓度。

     

    Abstract: This study was aimed to determine the hepatic and small intestinal distribution of active lignans in rats after treated with Wuzhi tablet (WZ, Schisandra sphenanthera extract) by LC-MS/MS method. Male Sprague-Dawley rats were sacrificed at 0.25, 1.5, 4, 6, 10, 24 h after an oral administration of WZ, and then hepatic and small intestinal samples were collected for analysis. The results showed that concentrations of lignans in liver and small intestine of rats were decreased with WZ pretreated time. The concentrations of all lignans in rat liver and small intestine at 0.25 h were the highest after a single oral administration. All lignans was undetectable in all tissues 24 h after oral dosing, suggesting lignans of WZ were eliminated rapidly in rats. The concentrations of schisandrin A, schisandrol B and schisantherin A in small intestine were much higher than those in the liver, suggesting the effect of WZ on the intestinal metabolism enzyme might be more potent than that on the liver. In short, the current results suggest that lignans of WZ were not accumulated in rat liver and small intestine. The concentrations of lignans of WZ in small intestine were much higher than those in liver.

     

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