Inhibitory Effect of Oxethazaine on Midazolam Metabolism in Rats

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  • Namba Hokuto
    Department of Pharmacology, Showa University, School of Medicine
  • Nishimura Yuki
    Department of Pharmacology, Showa University, School of Medicine
  • Kurata Norimitsu
    Faculty of Arts and Sciences at Fujiyoshida, Showa University
  • Iwase Mariko
    Department of Pharmacology, Showa University, School of Medicine
  • Hirai Takahito
    Department of Pharmacology, Showa University, School of Medicine
  • Kiuchi Yuji
    Department of Pharmacology, Showa University, School of Medicine

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<p>There have been few reports concerning to the drug–drug interactions (DDIs) with OTC drugs although an increase in the use of OTC drugs in recent years. This current study was conducted to clarify the DDIs through CYP3A inhibition by oxethazaine (OXZ), an antacid available as an OTC drug. Midazolam (MDZ) was used as a probe drug for CYP3A activity. In an in vivo study, a single oral dose of OXZ (50 mg/kg) was administered to rats 30, 60, or 120 min before oral MDZ administration (15 mg/kg). Serum concentrations of MDZ were analyzed by HPLC, and its pharmacokinetic parameters were compared with a water-treated control group. The inhibitory effect of OXZ on MDZ 1′-hydroxylation (MDZ 1′-OH) activity was investigated in vitro using rat liver and intestinal microsomes. Pretreatment of OXZ 120 min before MDZ administration significantly increased the area under the serum concentration–time curve (AUC0–∞) of MDZ six-fold compared to the control group without a change in elimination half-life (t1/2). In contrast, OXZ pretreatment 30 or 60 min before MDZ administration did not show any remarkable change in MDZ pharmacokinetic parameters. The in vitro study showed that OXZ inhibited MDZ 1′-OH activity in a concentration-dependent manner both in liver and intestinal microsomes. These results suggested that OXZ increases serum MDZ concentration presumably by the inhibition of liver and/or intestinal CYP3A activity. OXZ was predicted to cause the DDIs mediated by CYP3A inhibition, although this effect depended on the dose interval.</p>

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