Wang Rui, Zheng Kai, Liu Yunjiao, Ji Shuxia, Tang Yaxin, Wang Jie, Jiang Rong
Department of Pharmacy, Shanghai Zhongye Hospital, Shanghai, China.
Department of Pharmacy, Shanghai Baoshan Luodian Hospital, Shanghai, China.
Xenobiotica. 2024 Feb;54(2):57-63. doi: 10.1080/00498254.2023.2301352. Epub 2024 Jan 12.
This study assessed the effect of tubeimoside I on CYP1A2, 2A6, 2C8, 2C9, 2C19, 2D6, 2E1, and 3A4 to reveal the potential of tubeimoside I to induce drug-drug interaction.The evaluation of cytochromes P450 enzyme (CYP) activity was performed in pooled human liver microsomes with probing substrates of CYP1A2, 2A6, 2C8, 2C9, 2C19, 2D6, 2E1, and 3A4. Typical inhibitors were employed as positive controls and the effect of 0, 2.5, 5, 10, 25, 50, and 100 μM tubeimoside I was investigated.The activity of CYP2D6, 2E1, and 3A4 was significantly inhibited by tubeimoside I with the IC values of 10.34, 11.58, and 9.74 μM, respectively. The inhibition of CYP2D6 and 2E1 was competitive with the value of 5.66 and 5.29 μM, respectively. While the inhibition of CYP3A4 was non-competitive with the value of 4.87 μM. Moreover, the inhibition of CYP3A4 was time-dependent with the and values of 0.635 μM and 0.0373 min, respectively.Tubeimoside I served as a competitive inhibitor of CYP2D6 and 2E1 exerting weak inhibition and a non-competitive inhibitor of CYP3A4 exerting moderate inhibition.
本研究评估了土贝母苷甲对CYP1A2、2A6、2C8、2C9、2C19、2D6、2E1和3A4的影响,以揭示土贝母苷甲诱导药物相互作用的可能性。在人肝微粒体中使用CYP1A2、2A6、2C8、2C9、2C19、2D6、2E1和3A4的探针底物进行细胞色素P450酶(CYP)活性评估。使用典型抑制剂作为阳性对照,研究了0、2.5、5、10、25、50和100μM土贝母苷甲的作用。土贝母苷甲显著抑制CYP2D6、2E1和3A4的活性,IC值分别为10.34、11.58和9.74μM。CYP2D6和2E1的抑制作用具有竞争性,其Ki值分别为5.66和5.29μM。而CYP3A4的抑制作用为非竞争性,Ki值为4.87μM。此外,CYP3A4的抑制作用具有时间依赖性,K_i和k_inact值分别为0.635μM和0.0373min。土贝母苷甲作为CYP2D6和2E1的竞争性抑制剂,抑制作用较弱;作为CYP3A4的非竞争性抑制剂,抑制作用中等。