TY - JOUR T1 - Reversible and Irreversible Inhibition of Cytochrome P450 Enzymes by Methylophiopogonanone A JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 459 LP - 469 DO - 10.1124/dmd.120.000325 VL - 49 IS - 6 AU - Dong-Zhu Tu AU - Xu Mao AU - Feng Zhang AU - Rong-Jing He AU - Jing-Jing Wu AU - Yue Wu AU - Xiao-Hua Zhao AU - Jiang Zheng AU - Guang-Bo Ge Y1 - 2021/06/01 UR - http://dmd.aspetjournals.org/content/49/6/459.abstract N2 - Methylophiopogonanone A (MOA), an abundant homoisoflavonoid bearing a methylenedioxyphenyl moiety, is one of the major constituents in the Chinese herb Ophiopogon japonicas. This work aims to assess the inhibitory potentials of MOA against cytochrome P450 enzymes and to decipher the molecular mechanisms for P450 inhibition by MOA. The results showed that MOA concentration-dependently inhibited CYP1A, 2C8, 2C9, 2C19, and 3A in human liver microsomes (HLMs) in a reversible way, with IC50 values varying from 1.06 to 3.43 μM. By contrast, MOA time-, concentration-, and NADPH-dependently inhibited CYP2D6 and CYP2E1, along with KI and kinact values of 207 µM and 0.07 minute−1 for CYP2D6, as well as 20.9 µM and 0.03 minutes−1 for CYP2E1. Further investigations demonstrated that a quinone metabolite of MOA could be trapped by glutathione in an HLM incubation system, and CYP2D6, 1A2, and 2E1 were the major contributors to catalyze the metabolic activation of MOA to the corresponding O-quinone intermediate. Additionally, the potential risks of herb-drug interactions triggered by MOA or MOA-related products were also predicted. Collectively, our findings verify that MOA is a reversible inhibitor of CYP1A, 2C8, 2C9, 2C19, and 3A but acts as an inactivator of CYP2D6 and CYP2E1.Significance Statement Methylophiopogonanone A (MOA), an abundant homoisoflavonoid isolated from the Chinese herb Ophiopogon japonicas, is a reversible inhibitor of CYP1A, 2C8, 2C9, 2C19, and 3A but acts as an inactivator of CYP2D6 and CYP2E1. Further investigations demonstrated that a quinone metabolite of MOA could be trapped by glutathione in a human liver microsome incubation system, and CYP2D6, 1A2, and 2E1 were the major contributors to catalyze the metabolic activation of MOA to the corresponding O-quinone intermediate. ER -