PHENYTOIN CAUSES A RAPID INCREASE IN 6-BETA-HYDROXYCORTISOL URINARY-EXCRETION IN HUMANS - A PUTATIVE MEASURE OF CYP3A INDUCTION

This study was conducted in eight healthy volunteers to assess the tim e course of induction of cytochrome P-450 by phenytoin. Subjects recei ved 200 mg of phenytoin every 8 h for 11 doses and 100 mg every 8 h fo r 8 doses. Trough concentrations of phenytoin in plasma were measured by HPLC, Urine samples were collected between 08:00 and 12:00 on days -1, 1, 2, 3, 4, 5, and 7. Urinary concentrations of 6 beta-hydroxycort isol (6 beta-OHC) and cortisol (C) were determined by HPLC and were re ported as a ratio (6 beta-OHC/C); this ratio is a marker for the 3A is ozyme family of cytochrome P-450 (CYP3A). Mean plasma phenytoin concen trations on day 7 were 15.4 +/- 7.20 mu g/mL. Mean 6 beta-OHC/C ratios increased by a factor of 2.37 from baseline during the course of the study. Values for the ratios on days 4, 5, and 7 were significantly hi gher than baseline by Dunnett's test (one-sided) (p < 0.05); the day 3 value was borderline statistically significant. These results show th at phenytoin rapidly induces the activity of the CYP3A family of isozy mes, with effects apparent within 48 h after the initiation of phenyto in therapy.