覃小玲, 段文海, 李嘉丽, 黄民, 毕惠嫦. 五酯片提取物对人CYP3A4及CYP3A5重组酶活性的抑制作用及其机制J. 药学学报, 2022, 57(8): 2453-2460. DOI: 10.16438/j.0513-4870.2022-0651
引用本文: 覃小玲, 段文海, 李嘉丽, 黄民, 毕惠嫦. 五酯片提取物对人CYP3A4及CYP3A5重组酶活性的抑制作用及其机制J. 药学学报, 2022, 57(8): 2453-2460. DOI: 10.16438/j.0513-4870.2022-0651
QIN Xiao-ling, DUAN Wen-hai, LI Jia-li, HUANG Min, BI Hui-chang. Mechanistic understanding of the inhibitory effect of cytochrome P450 3A4 and 3A5 by Wuzhi tablet (Schisandra sphenanthera extract)J. Acta Pharmaceutica Sinica, 2022, 57(8): 2453-2460. DOI: 10.16438/j.0513-4870.2022-0651
Citation: QIN Xiao-ling, DUAN Wen-hai, LI Jia-li, HUANG Min, BI Hui-chang. Mechanistic understanding of the inhibitory effect of cytochrome P450 3A4 and 3A5 by Wuzhi tablet (Schisandra sphenanthera extract)J. Acta Pharmaceutica Sinica, 2022, 57(8): 2453-2460. DOI: 10.16438/j.0513-4870.2022-0651

五酯片提取物对人CYP3A4及CYP3A5重组酶活性的抑制作用及其机制

Mechanistic understanding of the inhibitory effect of cytochrome P450 3A4 and 3A5 by Wuzhi tablet (Schisandra sphenanthera extract)

  • 摘要: 五酯片是临床上常用的护肝中药单方制剂, 常被用来治疗各种原因引起的肝损伤。前期研究表明五酯片可通过抑制CYP3A从而升高移植患者、大鼠体内他克莫司、环孢素、紫杉醇等药物的血药浓度。CYP3A4和CYP3A5是CYP3A的两种重要亚型, 但它们在催化活性及对抑制剂敏感性上表现不同。对CYP3A4和CYP3A5抑制作用的差异可能会导致不同的药物相互作用, 这种相互作用的风险在体内可能会被进一步放大。可见, 研究五酯片对CYP3A4及CYP3A5活性抑制作用的异同具有较好的临床治疗学及经济学意义。然而, 目前尚未见五酯片对CYP3A4及CYP3A5活性的抑制作用及作用机制的相关研究。因此, 本研究利用人重组CYP3A4 (recombinant human CYP3A4, rhCYP3A4)、人重组CYP3A5 (recombinant human CYP3A5, rhCYP3A5) 考察五酯片提取物对CYP3A4、CYP3A5活性的影响及作用特征、机制。结果表明, 五酯片提取物对CYP3A4、CYP3A5活性的抑制作用存在NADPH、预孵育时间及浓度依赖性; 其与CYP3A4及CYP3A5的结合比较牢固, 不能通过透析来消除; 其对CYP3A5的抑制作用稍强于其对CYP3A4的抑制作用。因此, 临床上合用五酯片时, 要警惕由此引起的中西药药物相互作用。

     

    Abstract: Wuzhi tablet (WZ) is a prescribed herbal medicine extracted from Schisandra sphenanthera, which is widely used to protect the liver injury and drug-induced hepatotoxicity in clinical practices. Previous studies showed that WZ significantly increased the blood concentrations of tacrolimus, cyclosporine A, paclitaxel by inhibiting the cytochrome P450 3A (CYP3A)-mediated metabolism. CYP3A4 and CYP3A5 are the most important isoenzymes among the CYP3A subfamily. However, there are some differences in the catalytic and inhibitory activities between CYP3A4 and CYP3A5, which may lead to different risk of drug-drug and herb-drug interactions, and the risks may be further amplified in vivo. Currently, few reports have compared the herbal medicine inhibitory effects between CYP3A4 and CYP3A5 mediated metabolic reactions. Therefore, detailing the inhibitory effect of WZ on CYP3A4 and CYP3A5 will help understand and predict the potential herb-drug interaction. The results showed that WZ inhibited CYP3A4 and CYP3A5 in a NADPH-, time- and concentration- dependent manner. WZ showed more potent inhibition on CYP3A5 than CYP3A4. Cautions warranted when combining WZ with other therapeutic drugs to avoid the potential herb-drug interaction.

     

/

返回文章
返回