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Effect of milk thistle (Silybum marianum) and black cohosh (Cimicifuga racemosa) supplementation on digoxin pharmacokinetics in humans

机译:补充水飞蓟(Silybum marianum)和黑升麻(Cimicifuga racemosa)对人体中地高辛药代动力学的影响

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摘要

Phytochemical-mediated modulation of p-glycoprotein (P-gp) and other drug transporters may underlie many herb-drug interactions. Serial plasma concentration-time profiles of the P-gp substrate, digoxin, were used to determine whether supplementation with milk thistle or black cohosh modified P-gp activity in vivo. Sixteen healthy volunteers were randomly assigned to receive a standardized milk thistle (900 mg daily) or black cohosh (40 mg daily) supplement for 14 days, followed by a 30-day washout period. Subjects were also randomized to receive rifampin (600 mg daily, 7 days) and clarithromycin (1000 mg daily, 7 days) as positive controls for P-gp induction and inhibition, respectively. Digoxin (Lanoxicaps®, 0.4 mg) was administered orally before and at the end of each supplementation and control period. Serial digoxin plasma concentrations were obtained over 24 hours and analyzed by chemiluminescent immunoassay. Comparisons of AUC(0–3), AUC(0–24), Cmax,, CL/F, and elimination half-life were used to assess the effects of milk thistle, black cohosh, rifampin, and clarithromycin on digoxin pharmacokinetics. Rifampin produced significant reductions (p<0.01) in AUC(0–3), AUC(0–24) and Cmax, while clarithromycin increased these parameters significantly (p<0.01). Significant changes in digoxin half-life and CL/F were also observed with clarithromycin. No statistically significant effects on digoxin pharmacokinetics were observed following supplementation with either milk thistle or black cohosh, although digoxin AUC(0–3) and AUC(0–24) approached significance (p=0.06) following milk thistle administration. When compared to rifampin and clarithromycin, supplementation with these specific formulations of milk thistle or black cohosh did not appear to affect digoxin pharmacokinetics, suggesting that these supplements are not potent modulators of P-gp in vivo.
机译:植物化学介导的对p-糖蛋白(P-gp)和其他药物转运蛋白的调节可能是许多草药与药物相互作用的基础。 P-gp底物地高辛的系列血浆浓度-时间曲线用于确定是否补充乳蓟或黑升麻在体内修饰了P-gp活性。随机分配16名健康志愿者接受标准的水飞蓟(每天900毫克)或黑升麻(每天40毫克)补充,持续14天,然后进行30天的清除期。受试者也被随机分为分别接受利福平(每天600 mg,7天)和克拉霉素(每天1000 mg,7天)作为P-gp诱导和抑制的阳性对照。在每个补充和对照期之前和结束时口服地高辛(Lanoxicaps ®,0.4 mg)。在24小时内获得了连续的地高辛血浆浓度,并通过化学发光免疫分析法进行了分析。通过比较AUC(0-3),AUC(0-24),Cmax,CL / F和消除半衰期来评估水飞蓟,黑升麻,利福平和克拉霉素对地高辛药代动力学的影响。利福平使AUC(0–3),AUC(0–24)和Cmax显着降低(p <0.01),而克拉霉素显着降低了这些参数(p <0.01)。克拉霉素也可观察到地高辛半衰期和CL / F的显着变化。补充乳蓟或黑升麻后,未观察到对地高辛药代动力学的统计学显着影响,尽管乳蓟给药后地高辛AUC(0-3)和AUC(0-24)接近显着性(p = 0.06)。与利福平和克拉霉素相比,添加这些特定配方的水飞蓟或黑升麻似乎没有影响地高辛的药代动力学,这表明这些补充剂不是体内P-gp的有效调节剂。

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