Laboratory of Clinical Pharmacokinetics, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Br J Clin Pharmacol. 2010 Jun;69(6):656-62. doi: 10.1111/j.1365-2125.2010.03624.x.
To assess the effect of danshen extract on CYP3A4 activity using midazolam as an in vivo probe.
A sequential, open-label, two-period pharmacokinetic interaction study design was used to compare midazolam pharmacokinetic parameters before and after 14 days of administration of danshen tablets. Twelve healthy volunteers received a single oral dose (15 mg) of midazolam followed by danshen tablets (four tablets orally, three times a day) for 14 days. On the last day of the study they received four danshen tablets with a 15 mg midazolam tablet and plasma concentrations of midazolam and its corresponding metabolite 1-hydroxylmidazolam were measured prior to and after the administration of danshen tablets periodically for 12 h.
The 90% confidence intervals of C(max,)t(1/2), CL/F and AUC(0,infinity) of midazolam before and after administration of danshen tablets were (0.559, 0.849), (0.908, 1.142), (1.086, 1.688) and (0.592, 0.921), respectively; and those of C(max), t(1/2) and AUC(0,infinity) of 1-hydroxylmidazolam after vs. before administration of danshen tablets were (0.633, 0.923), (0.801, 1.210) and (0.573, 0.980), respectively. Ratios of geometric LS means of C(max(1OHMid)) : C(max(Mid)) and AUC(max(1OHMid)) : AUC(max(Mid)) (after vs. before 14-day danshen) were 1.072 and 1.035, respectively.
Our findings suggest that multiple dose administration of danshen tablets may induce CYP3A4 in the gut. Accordingly, caution should be taken when danshen products are used in combination with therapeutic drugs metabolized by CYP3A.
以咪达唑仑为体内探针,评估丹参提取物对 CYP3A4 活性的影响。
采用序贯、开放标签、两周期药代动力学相互作用研究设计,比较 14 天丹参片给药前后咪达唑仑药代动力学参数。12 名健康志愿者单次口服咪达唑仑(15mg)后,14 天内口服丹参片(4 片,每日 3 次)。研究的最后一天,他们在口服 4 片丹参片后 15 分钟内口服 1 片咪达唑仑片,并在服用丹参片前后定期测量 12 小时内咪达唑仑及其相应代谢物 1-羟基咪达唑仑的血浆浓度。
咪达唑仑给药前后的 C(max,)t(1/2)、CL/F 和 AUC(0,infinity)的 90%置信区间分别为(0.559,0.849)、(0.908,1.142)、(1.086,1.688)和(0.592,0.921);1-羟基咪达唑仑给药前后的 C(max)、t(1/2)和 AUC(0,infinity)分别为(0.633,0.923)、(0.801,1.210)和(0.573,0.980)。C(max(1OHMid)):C(max(Mid))和 AUC(max(1OHMid)):AUC(max(Mid))(用药后与用药前 14 天丹参)的几何 LS 均值比值分别为 1.072 和 1.035。
我们的研究结果表明,丹参片多次给药可能诱导肠道中的 CYP3A4。因此,在使用丹参产品与经 CYP3A 代谢的治疗药物联合使用时应谨慎。