In-vivo and in-vitro metabolic clearance of midazolam, a cytochrome P450 3A substrate, by the liver under normal and increased enzyme activity in rats

The metabolic clearance of midazolam, a cytochrome P450 (CYP) 3A substrate, by the liver under normal and increased enzyme activity in rats was determ ined in-vivo and in-vitro to elucidate the reproducibility of the in-vivo h epatic extraction ratio of midazolam from the in-vitro study. The hepatic e nzyme activity was modified by pretreating rats with a CYP inducer such as dexamethasone and clotrimazole. The in-vivo hepatic extraction ratio (ERh,obs) Of midazolam under a steady- state plasma concentration (approx. 3 nmol mL(-1)) in untreated (control) r ats was 0.864. This value increased to 0.984 in dexamethasone-pretreated ra ts and to 0.964 in clotrimazole-pretreated rats. The in-vitro hepatic intri nsic clearance (CLint,in-vitro), expressed as mL min(-1) (mg microsomal pro tein)(-1) of midazolam was estimated as V-max (K-m)(-1) by in-vitro metabol ism studies using liver microsomes. The CLint,in-vitro value was converted to the CLint,cal value, expressed as mt min(-1) kg(-1). by considering the microsomal protein content (g liver)(-1) and the microsomal protein content (g liver)(-1) kg(-1). The estimated CLint,cal value was then converted to the ERh value (ERh,cal) according to the well-stirred, the parallel-tube an d the dispersion models. The ERh,cal values obtained by the parallel-tube m odel were in good agreement with corresponding in-vivo ERh,obs values. In conclusion, it was demonstrated that high hepatic clearances of midazola m under normal and increased CYP3A activity were reasonably predicted from in-vitro metabolism studies using liver microsomes.