Lei H-P, Yu X-Y, Xie H-T, Li H-H, Fan L, Dai L-L, Chen Y, Zhou H-H
Medical Research Center of Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Xenobiotica. 2010 Apr;40(4):275-81. doi: 10.3109/00498250903509383.
The objective of this study was to investigate the effects of continuous St. John's wort administration on single-dose pharmacokinetics of bupropion, a substrate of cytochrome P450 (CYP) 2B6, in healthy Chinese volunteers. Eighteen unrelated healthy male subjects participated in this study. The single-dose pharmacokinetics of bupropion and hydroxybupropion were determined before (control) and after a long-term period of St. John's wort intake (325 mg, three times a day for 14 days). Plasma concentrations of bupropion and hydroxybupropion were determined before and at 0.5, 1, 2, 3, 4, 5, 6, 8, 10, 12, 24, 36, 48, 60 and 72 h after dosing. St. John's wort treatment decreased the area under the concentration versus time curve extrapolated to infinity of bupropion in healthy volunteers from 1.4 microg.h ml(-1) (95% confidence interval [CI] = 1.2-1.6 microg.h ml(-1)) after bupropion alone to 1.2 microg.h ml(-1) (95% CI = 1.1-1.3 microg.h ml(-1)) during St. John's wort treatment. St. John's wort treatment increased the oral clearance of bupropion from 108.3 l h(-1) (95% CI = 95.4-123.0 l h(-1)) to 130.0 l h(-1) (95% CI = 118.4-142.7 l h(-1)). No change in the time to peak concentration (t(max)) and the blood elimination half-life (t(1/2)) of bupropion was observed between the control and St. John's wort-treated phases. However, the half-life of hydroxybupropion between two phases had a significant difference by a Student's t test after logarithmic transformation. St. John's wort treatment decreased the half-life of hydroxybupropion from 26.7 h (95% CI = 23.8-29.9 h) to 24.4 h (95% CI = 21.9-27.3 h). St. John's wort decreased, to a statistically significant extent, the plasma concentrations of bupropion, probably mainly by increasing the clearance of bupropion.
本研究的目的是调查在健康中国志愿者中,连续服用圣约翰草对细胞色素P450(CYP)2B6底物安非他酮单剂量药代动力学的影响。18名无亲缘关系的健康男性受试者参与了本研究。在长期服用圣约翰草(325毫克,每日三次,共14天)之前(对照)和之后,测定了安非他酮和羟基安非他酮的单剂量药代动力学。在给药前以及给药后0.5、1、2、3、4、5、6、8、10、12、24、36、48、60和72小时测定安非他酮和羟基安非他酮的血浆浓度。圣约翰草治疗使健康志愿者中安非他酮浓度-时间曲线外推至无穷大的面积从单独服用安非他酮后的1.4微克·小时·毫升-1(95%置信区间[CI]=1.2-1.6微克·小时·毫升-1)降至圣约翰草治疗期间的1.2微克·小时·毫升-1(95%CI=1.1-1.3微克·小时·毫升-1)。圣约翰草治疗使安非他酮的口服清除率从108.3升·小时-1(95%CI=9५.4-123.0升·小时-1)增加至130.0升·小时-1(95%CI=118.4-142.7升·小时-1)。在对照期和圣约翰草治疗期之间,未观察到安非他酮的达峰时间(t(max))和血液消除半衰期(t(1/2))有变化。然而,经对数转换后,通过学生t检验发现两个阶段之间羟基安非他酮半衰期有显著差异。圣约翰草治疗使羟基安非他酮的半衰期从26.7小时(95%CI=23.8-१9.9小时)降至24.4小时(95%CI=21.9-27.3小时)。圣约翰草在统计学上显著降低了安非他酮的血浆浓度,可能主要是通过增加安非他酮的清除率实现的。