Wang Zhiheng, Zhou Kuilong, Liang Zhijie, Zhang Huiting, Song Yangjie, Yang Xiaomin, Xiang Dongguo, Xie Qingfan
Department of Acupuncture, Xingtai People's Hospital, Hebei Medical University Affiliated Hospital, Xingtai, Hebei, China.
Internal Medicine of TCM, Xingtai People's Hospital, Hebei Medical University Affiliated Hospital, Xingtai, Hebei, China.
Planta Med. 2023 Jan;89(1):72-78. doi: 10.1055/a-1806-2935. Epub 2022 May 6.
Dendrobine is the major active ingredient of , and , all of which are used in traditional Chinese medicine owing to their antitumor and anti-inflammation activities. Hence, investigation on the interaction of dendrobine with cytochrome P450 enzymes could provide a reference for the clinical application of . The effects of dendrobine on cytochrome P450 enzymes activities were investigated in the presence of 0, 2.5, 5, 10, 25, 50, and 100 µM dendrobine in pooled human liver microsomes. The specific inhibitors were employed as the positive control and the blank groups were set as the negative control. The Lineweaver-Burk plots were plotted to characterize the specific inhibition model and obtain the kinetic parameters. The study reveals that dendrobine significantly inhibited the activity of CYP3A4, 2C19, and 2D6 with IC values of 12.72, 10.84, and 15.47 µM, respectively. Moreover, the inhibition of CYP3A4 was found to be noncompetitive ( = 6.41 µM) and time dependent ( = 2.541 µM, = 0.0452 min), while the inhibition of CYP2C19 and 2D6 was found to be competitive with the values of 5.22 and 7.78 µM, respectively, and showed no time-dependent trends. The inhibitory effect of dendrobine implies the potential drug-drug interaction between dendrobine and CYP3A4-, 2C9-, and 2D6-metabolized drugs. Nonetheless, these findings need further validation.
石蒜碱是[具体药物名称1]、[具体药物名称2]和[具体药物名称3]的主要活性成分,由于它们具有抗肿瘤和抗炎活性,在中国传统医学中均有应用。因此,研究石蒜碱与细胞色素P450酶的相互作用可为[具体药物名称1]、[具体药物名称2]和[具体药物名称3]的临床应用提供参考。在含有0、2.5、5、10、25、50和100 μM石蒜碱的人肝微粒体中,研究了石蒜碱对细胞色素P450酶活性的影响。使用特异性抑制剂作为阳性对照,设置空白组作为阴性对照。绘制Lineweaver-Burk图以表征特异性抑制模型并获得动力学参数。研究表明,石蒜碱显著抑制CYP3A4、2C19和2D6的活性,IC值分别为12.72、10.84和15.47 μM。此外,发现对CYP3A4的抑制是非竞争性的(Ki = 6.41 μM)且具有时间依赖性(K0.5 = 2.541 μM,kinact = 0.0452 min),而对CYP2C19和2D6的抑制是竞争性的,Ki值分别为5.22和7.78 μM,且无时间依赖性趋势。石蒜碱的抑制作用表明其与CYP3A4、2C9和2D6代谢药物之间可能存在药物相互作用。尽管如此,这些发现仍需进一步验证。