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- W2912241303 abstract "Clopidogrel acyl-<i>β</i>-d-glucuronide is a mechanism-based inhibitor of cytochrome P450 2C8 in human liver microsomes (HLMs). However, time-dependent inactivation (TDI) of CYP2C8 could not be detected in an earlier study in human recombinant CYP2C8 (Supersomes). Here, we investigate whether different enzyme sources exhibit differences in detection of CYP2C8 TDI under identical experimental conditions. Inactivation of CYP2C8 by amiodarone (100 <i>μ</i>M), clopidogrel acyl-<i>β</i>-d-glucuronide (100 <i>μ</i>M), gemfibrozil 1<i>-O-β</i>-glucuronide (100 <i>μ</i>M), and phenelzine (100 <i>μ</i>M) was investigated in HLMs and three recombinant human CYP2C8 preparations (Supersomes, Bactosomes, and EasyCYP Bactosomes) using amodiaquine <i>N</i>-deethylation as the marker reaction. Furthermore, the inactivation kinetics of CYP2C8 by clopidogrel glucuronide (5–250 <i>μ</i>M) was determined in Supersomes and Bactosomes. Amiodarone caused weak TDI in all enzyme preparations tested, while the extent of inactivation by clopidogrel glucuronide, gemfibrozil glucuronide, and phenelzine varied markedly between preparations, and even different Supersome lots. Both glucuronides caused strong inactivation of CYP2C8 in HLMs, Bactosomes and in one Supersome lot (>50% inhibition), but significant inactivation could not be reliably detected in other Supersome lots or EasyCYP Bactosomes. In Bactosomes, the concentration producing half of k<sub>inact</sub> (K<sub>I</sub>) and maximal inactivation rate (k<sub>inact</sub>) of clopidogrel glucuronide (14 <i>μ</i>M and 0.054 minute<sup>−1</sup>) were similar to those determined previously in HLMs. Phenelzine caused strong inactivation of CYP2C8 in one Supersome lot (91% inhibition) but not in HLMs or other recombinant CYP2C8 preparations. In conclusion, different enzyme sources and different lots of the same recombinant enzyme preparation are not equally sensitive to detect inactivation of CYP2C8, suggesting that recombinant CYPs should be avoided when identifying mechanism-based inhibitors." @default.
- W2912241303 created "2019-02-21" @default.
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- W2912241303 date "2019-02-01" @default.
- W2912241303 modified "2023-10-17" @default.
- W2912241303 title "Critical Differences between Enzyme Sources in Sensitivity to Detect Time-Dependent Inactivation of CYP2C8" @default.
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- W2912241303 doi "https://doi.org/10.1124/dmd.118.085498" @default.
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