Influence of St. John's Wort on Intravenous Fentanyl Pharmacokinetics, Pharmacodynamics, and Clinical Effects A Randomized Clinical Trial

被引:10
|
作者
Loughren, Michael J. [1 ,3 ]
Kharasch, Evan D. [2 ]
Kelton-Rehkopf, Megan C. [4 ]
Syrjala, Karen L. [4 ]
Shen, Danny D. [3 ,4 ]
机构
[1] Madigan Army Med Ctr, Dept Anesthesia & Operat Serv, Tacoma, WA 98431 USA
[2] Duke Univ, Sch Med, Dept Anesthesiol, Durham, NC USA
[3] Univ Washington, Sch Pharm, Dept Pharmaceut, Seattle, WA 98195 USA
[4] Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA
基金
美国国家卫生研究院;
关键词
PREGNANE-X-RECEPTOR; ALTERNATIVE MEDICINE USE; BLOOD-BRAIN-BARRIER; P-GLYCOPROTEIN; HYPERICUM-PERFORATUM; CYTOCHROME-P450; 3A4; DRUG-INTERACTIONS; TRANSPORT; DISPOSITION; METABOLISM;
D O I
10.1097/ALN.0000000000003065
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Patients often use complementary and alternative herbal medicines, hence, potential exists for adverse herb-drug interactions. Fentanyl is metabolized by hepatic CYP3A4 and considered transported by blood-brain barrier P-glycoprotein. Both disposition processes could be upregulated by the herbal St. John's wort. This investigation evaluated effects of St. John's wort on fixed-dose and apparent steady-state IV fentanyl pharmacokinetics, pharmacodynamics, and clinical effects. Methods: Healthy volunteers received a fentanyl fixed-dose infusion and an individually tailored target controlled infusion on separate days, before and after 30-day St. John's wort (300 mg thrice daily; n = 8) or placebo control (n = 8) in a randomized parallel-group design. Fentanyl plasma concentrations, pupil diameter, analgesic response to experimental pain (cold pressor), subjective side effects, and cognitive effects were measured. Plasma fentanyl concentrations and changes in pupil diameter were subjected to pharmacokinetic-pharmacodynamic modeling. Results: St. John's wort did not alter fentanyl pharmacokinetics. Clearance (l/min) before and after St. John's wort (1.13 +/- 0.29 and 1.24 +/- 0.26, respectively) or placebo (0.96 +/- 0.28 and 1.12 +/- 0.27, respectively) were not different. St. John's wort also did not affect fentanyl pharmacodynamics as measured by pupil constriction after fixed-dose and tailored fentanyl infusions. EC50 (ng/ml) was 1.1 +/- 0.7 and 1.4 +/- 0.9 before and after St. John's wort versus 1.2 +/- 0.8 and 1.4 +/- 1.7 before and after placebo. Effect site equilibration time, T-1/2,T-ke0 (min), was 12.8 +/- 5.3 and 11.3 +/- 6.4 before and after St. John's wort versus 11.4 +/- 6.4 and 11.1 +/- 5.6 before and after placebo. St. John's wort had no influence on analgesia, cognitive performance, or somatic cognitive-affective effects of fentanyl. Conclusions: St. John's wort did not alter fentanyl pharmacokinetics, pharmacodynamics or clinical effects, suggesting no effect on hepatic clearance or blood-brain barrier efflux. Patients taking St. John's wort will likely not respond differently to IV fentanyl for anesthesia or analgesia.
引用
收藏
页码:491 / 503
页数:13
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