Prediction of drug–drug interactions with carbamazepine-10, 11-epoxide using a new in vitro assay for epoxide hydrolase inhibition. (1st December 2016)

• Record Type: Journal Article
• Authors: Rosa, Maria; Bonnaillie, Pierre; Chanteux, Hugues
• Is Part Of: Xenobiotica. Volume 46:Number 12(2016:Dec.)
• Page Start: 1076
• Page End: 1084
• Publication Date: 2016-12-01
• Subjects: DDI -- enzyme inhibition -- epoxide hydrolase; Metabolism -- Periodicals; Drugs -- Physiological effect -- Periodicals; Food additives -- Periodicals; Chemicals -- Physiological effect -- Periodicals; Biochemistry -- Periodicals; Pharmaceutical Preparations -- metabolism -- Periodicals; Metabolism -- Periodicals; 574.133
• DOI: 10.3109/00498254.2016.1151088
• Languages: English
• ISSNs: 0049-8254

Abstract

Abstract: 1. Carbamazepine is an antiepileptic drug which is metabolized by CYP3A4 into carbamazepine-10, 11-epoxide. This metabolite is then detoxified by epoxide hydrolase. As carbamazepine-10, 11-epoxide has been associated with neurotoxicity, it is critical to identify whether a new antiepileptic drug has the potential to inhibit epoxide hydrolase and therefore increase carbamazepine-10, 11-epoxide plasma levels. 2. In this study, an in vitro assay was developed to evaluate epoxide hydrolase activity by using carbamazepine-10, 11-epoxide as probe substrate. The ability of this assay to predict drug–drug interactions (DDI) at the epoxide hydrolase level was also investigated. 3. To this aim, known inhibitors of epoxide hydrolase for which in vivo data are available were used. Firstly, carbamazepine-10, 11-epoxide hydrolase activity was determined in liver microsomes, cytosol and hepatocytes. Thereafter, the IC50 of epoxide hydrolase inhibitors (progabide, valproic acid, valpromide and valnoctamide) was determined in liver microsomes and hepatocytes. Finally, prediction of AUC increase was performed using the in vitro data generated. 4. Interestingly, epoxide hydrolase activity was found to be much higher in human hepatocytes compared to liver microsomes/cytosol. Even though assessed on a limited number of compounds, this study demonstrated that the use of hepatocytes seems to be a more relevant model to assess and predict DDI at the epoxide hydrolase level.