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• W1924352418 abstract "Abstract Menthol is used widely as a constituent of functional foods and chemical drugs. The present study investigated changes in the pharmacokinetic behavior of intravenously administered midazolam (MDZ), a probe for CYP3A, when rats were treated with menthol. The study also examined which isoforms of CYP3A1 and 3A2 were menthol‐inducible and contributed to the altered disposition of midazolam. Menthol was administered intraperitoneally to rats once daily for 3 days at a dose of 10 mg/kg, while the control rats received vehicle alone. The pharmacokinetic examination of i.v. administered midazolam revealed that serum midazolam concentrations at each sampling point were lower in the menthol‐treated rats than in the control rats. Regarding the pharmacokinetic parameters of the menthol‐treated group, the area under the curve ( AUC ) was decreased significantly and, correspondingly, the elimination rate constant at terminal phase ( k e ) was increased significantly without significant changes in the volume of distribution at steady state ( V d ss ). The metabolic production of the 1′‐hydroxylated and 4′‐hydroxylated forms of MDZ by hepatic microsomes was significantly greater in the menthol‐treated rats than in the control rats. The expression levels of mRNA and protein for hepatic CYP3A2 were more than 2.5‐fold higher than the control levels when the rats were treated with menthol, whereas no changes were observed in the expression levels of CYP3A1. These results indicate that menthol enhanced the elimination clearance of midazolam by inducing hepatic CYP3A2 and that careful attention should be paid when menthol is ingested in combination with drugs that act as substrates for CYP3A. Copyright © 2014 John Wiley & Sons, Ltd." @default.
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• W1924352418 date "2015-01-24" @default.
• W1924352418 modified "2023-10-16" @default.
• W1924352418 title "Change in pharmacokinetic behavior of intravenously administered midazolam due to increased CYP3A2 expression in rats treated with menthol" @default.
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• W1924352418 doi "https://doi.org/10.1002/bdd.1930" @default.
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