4.7 Article

Potential herb-drug interaction risk of thymoquinone and phenytoin

Journal

CHEMICO-BIOLOGICAL INTERACTIONS
Volume 353, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.cbi.2022.109801

Keywords

Thymoquinone; Phenytoin; N.sativa; Herb-drug interactions

Funding

  1. National Key Research and Development Program of China [2017YFC1702006]
  2. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Re-sources (Guangxi Normal University) [CMEMR2020-B09]
  3. Funda-mental Research Funds for the Central Universities [DUT21LK11]
  4. China Postdoctoral Science Foundation [2019M651988]
  5. Post-doctoral Science Foundation in Jiangsu Province [2018K083B]
  6. Yangzhou Key Research and Development projects [YZ2020084]

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Thymoquinone, a bioactive compound of Nigella sativa L., has been shown to have neuroprotective and antiepileptic effects. This study investigated the potential drug interaction between thymoquinone and phenytoin, a commonly used drug for seizures. The results suggest that thymoquinone may inhibit the metabolism of phenytoin and caution should be taken when co-administering these two substances.
Thymoquinone is a main bioactive compound of Nigella sativa L. (N.sativa), which has been used for clinical studies in the treatment of seizures due to its beneficial neuroprotective activity and antiepileptic effects. It has been evidenced that thymoquinone may inhibit the activity of cytochrome P450 2C9 (CYP2C9). However, little is known about the effect of thymoquinone or N.sativa on the pharmacokinetic behavior of phenytoin, a second-line drug widely used in the management of status epilepticus. In this study, we systematically investigated the risk of the potential pharmacokinetic drug interaction between thymoquinone and phenytoin. The inhibitory effect of thymoquinone on phenytoin hydroxylation activity by CYP2C9 was determined using UPLC-MS/MS by measuring the formation rates for p-hydroxyphenytoin (p-HPPH). The potential for drug-interaction between thymoquinone and phenytoin was quantitatively predicted by using in vitro-in vivo extrapolation (IVIVE). Our data demonstrated that thymoquinone displayed effective inhibition against phenytoin hydroxylation activity. Enzyme kinetic studies showed that thymoquinone exerted a competitive inhibition against phenytoin hydroxylation with a K-i value of 4.45 +/- 0.51 mu M. The quantitative prediction from IVIVE suggested that the co administration of thymoquinone (> 18 mg/day) or thymoquinone-containing herbs (N.sativa > 1 g/day or N. sativa oil > 1 g/day) might result in a clinically significant herb-drug interactions. Additional caution should be taken when thymoquinone or thymoquinone-containing herbs are co-administered with phenytoin, which may induce unexpected potential herb-drug interactions via the inhibition of CYP2C9.

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