Effect of atorvastatin and fluvastatin on the metabolism of midazolam by cytochrome P450 in vitro

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Abstract

We have investigated the effects of the statins atorvastatin and fluvastatin on the cytochrome P450 3A4 enzyme (CYP 3A4)-mediated metabolism of midazolam in vitro, using pooled human liver microsomes. Midazolam was metabolised by human hepatic microsomes with a Michaelis-Menten constant (Km) of 5.25 (SD 1.2) μmol.1-1. Atorvastatin was a moderate competitive inhibitor of CYP 3A4 with an inhibitory constant (Ki) of 12.4 (95% CI 4.65-20.06) μmol.1-1. Fluvastatin was a weak non-competitive inhibitor of CYP 3A4 with a Ki of 94.3 (95% CI 55.01-133.5) μmol.1-1. Both atorvastatin and fluvastatin inhibit the CYP 3A4-mediated metabolism of midazolam in vitro. © 2005 Blackwell Publishing Ltd.

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Mc Donnell, C. G., Shorten, G., & Van Pelt, F. N. A. M. (2005). Effect of atorvastatin and fluvastatin on the metabolism of midazolam by cytochrome P450 in vitro. Anaesthesia, 60(8), 747–753. https://doi.org/10.1111/j.1365-2044.2005.04110.x

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