Journal of Korean Society for Clinical Pharmacology and Therapeutics (임상약리학회지)
- Volume 13 Issue 1
- /
- Pages.45-56
- /
- 2005
- /
- 1225-5467(pISSN)
Effect of Licorice (Radix Glycyrrhizae) Water Extract on the Pharmacokinetics and the Pharmacodynamics of Midazolam in Healthy Ssubjects
건강한 피험자에서 감초 수성추출물 복용이 midazolam의 약동 / 약력학에 미치는 효과
- Shon, Ji-Hong (Department of Pharmacology, Inje University College of Medicine) ;
- Park, Ji-Young (Department of Pharmacology, Gachon Medical School) ;
- Kim, Kyoung-Ah (Department of Pharmacology, Gachon Medical School) ;
- Yoon, Young-Ran (Department of Pharmacology, Inje University College of Medicine) ;
- Pyo, Ji-Soo (Department of Internal Medicine, Pusanpaik Hospital) ;
- Kim, Dong-Soo (Department of Internal Medicine, Pusanpaik Hospital) ;
- Jeon, Byung-Hun (Department of Pathology, College of Oriental Medicine, Wonkwang University) ;
- Cha, In-Jun (Department of Pharmacology, Inje University College of Medicine) ;
- Shin, Jae-Gook (Department of Pharmacology, Inje University College of Medicine)
- 손지홍 (인제대학교 의과대학 약리학교실) ;
- 박지영 (가천의대 약리학교실) ;
- 김경아 (가천의대 약리학교실) ;
- 윤영란 (인제대학교 의과대학 약리학교실) ;
- 표지수 (부산백병원 내과학교실) ;
- 김동수 (부산백병원 내과학교실) ;
- 전병훈 (원광대학교 한의과대학) ;
- 차인준 (인제대학교 의과대학 약리학교실) ;
- 신재국 (인제대학교 의과대학 약리학교실)
- Published : 2005.06.30
Abstract
Background : Licorice, a core traditional herbal medicine, is frequently coadministered with the conventional medications in Korea. Several reports suggested that the licorice treatment induced the cytochrome P450(CYP) in rats, especially for CYP3A isoform However, no report has been addressed to the effect of licorice on midazolam, CYP3A substrate, in human. This study was performed to evaluate the effect of licorice on the disposition and pharmacodynamic effects of midazolam in human. Methods : One gram of freeze dried water extract of licorice (extraction ratio ; 25%) or placebo were orally administered divided in two times to 10 healthy male subjects for 7 days as one blind randomized crossover manner with 2 weeks washout. On the day after completion of 7 days pretreatment, multiple blood samples were drawn and urine was collected for 24 hours after oral dose of 7.5 mg midazolam. Psychomotor performance tests including digit span test and digit symbol substitution test were conducted for 4 hours after midazolam administration on each phase of midazolam treatment and before pretreatment of placebo or licorice extract. The plasma concentration of midazolam and 1-hydroxymidazolam were determined with using HPLC and pharmacokinetic parameters were estimated by noncompartmental method. Results : After 1 week treatment of licorice extract, the plasma clearance of midazolam was significantly increased (1.15+0.50 vs 1.59+0.81 L/min, p<0.05) and the half-life was shortened ( 2.07+0.74 vs 1.34+0.60 hr, p<0.05) compared to those obtained after placebo treatment. Mean AUC of midazolam was decreased from 102.13+ 28.84 ng/ml hr to 85.06+48.51 ng/ml hr after licorice treatment, but not significantly different (p=0.11). There was no significant changes in AUC and urinary amount of 1-hydroxymidazolam by licorice pretreatment. The changes in the score of psychomotor performance tests (DST and DSST) measured after midazolam dosing were not significantly different between placebo and licorice pretreatment. Conclusions : Licorice water extract seems to affect the disposition of midazolam in human, but it is suggested that the CYP3A4 induction is not the major mechanism of the interaction. Further studies are remained to evaluate the mechanism of the pharmacokineitc interaction between midazolam and licorice water extract.