Supplementation with goldenseal (Hydrastis canadensis), but not kava kava (Piper methysticum), inhibits human CYP3A activity in vivo

被引:77
作者
Gurley, B. J. [1 ]
Swain, A. [2 ]
Hubbard, M. A. [1 ]
Hartsfield, F. [1 ]
Thaden, J. [5 ]
Williams, D. K. [3 ]
Gentry, W. B. [4 ]
Tong, Y. [1 ]
机构
[1] Univ Arkansas Med Sci, Coll Pharm, Dept Pharmaceut Sci, Little Rock, AR 72204 USA
[2] Univ Arkansas Med Sci, Coll Med, Gen Clin Res Ctr, Little Rock, AR USA
[3] Univ Arkansas Med Sci, Dept Biostat, Little Rock, AR USA
[4] Univ Arkansas Med Sci, Dept Anesthesiol, Little Rock, AR USA
[5] Univ Arkansas Med Sci, Little Rock, AR USA
关键词
D O I
10.1038/sj.clpt.6100222
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The effects of goldenseal (Hydrastis canadensis) and kava kava (Piper methysticum) supplementation on human CYP3A activity were evaluated using midazolam (MDZ) as a phenotypic probe. Sixteen healthy volunteers were randomly assigned to receive either goldenseal or kava kava for 14 days. Each supplementation phase was followed by a 30-day washout period. MDZ (8 mg, per os) was administered before and after each phase, and pharmacokinetic parameters were determined using standard non-compartmental methods. Comparisons of pre-and post-supplementation MDZ pharmacokinetic parameters revealed significant inhibition of CYP3A by goldenseal (AUC((0-infinity)), 107.9 +/- 743.3 vs 175.3 +/- 74.8 ng.h/ml; Cl/F/kg, 1.26 +/- 0.59 vs 0.81 +/- 0.45 l/h/kg; T-1/2, 2.01 +/- 0.42 vs 3.15 +/- 1.12 h; C-max, 50.6 +/- 26.9 vs 71.2 +/- 50.5 ng/ml). MDZ disposition was not affected by kava kava supplementation. These findings suggest that significant herb-drug interactions may result from the concomitant ingestion of goldenseal and CYP3A substrates.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 49 条
[1]
High-performance liquid chromatography determination of hydrastine and berberine in dietary supplements containing goldenseal [J].
Abourashed, EA ;
Khan, IA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (07) :817-822
[2]
Coma from the health food store: Interaction between kava and alprazolam [J].
Almeida, JC ;
Grimsley, EW .
ANNALS OF INTERNAL MEDICINE, 1996, 125 (11) :940-941
[3]
Pharmacokinetic and pharmacodynamic drug interactions with Kava (Piper methysticum Forst. f.) [J].
Anke, J ;
Ramzan, I .
JOURNAL OF ETHNOPHARMACOLOGY, 2004, 93 (2-3) :153-160
[4]
Brazier Nicole C, 2003, Am J Ther, V10, P163, DOI 10.1097/00045391-200305000-00003
[5]
An in vitro evaluation of human cytochrome P450 3A4 inhibition by selected commercial herbal extracts and tinctures [J].
Budzinski, JW ;
Foster, BC ;
Vandenhoek, S ;
Arnason, JT .
PHYTOMEDICINE, 2000, 7 (04) :273-282
[6]
Human cytochrome P450 inhibition and metabolic-intermediate complex formation by goldenseal extract and its methylenedioxyphenyl components [J].
Chatterjee, P ;
Franklin, MR .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (11) :1391-1397
[7]
Immunohistochemical analysis of expressions of hepatic cytochrome P450 in F344 rats following oral treatment with kava extract [J].
Clayton, Natasha P. ;
Yoshizawa, Katsuhiko ;
Kissling, Grace E. ;
Burka, Leo T. ;
Chan, Po-Chuen ;
Nyska, Abraham .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2007, 58 (04) :223-236
[8]
COHEN DR, 2002, MACWORLD, V19, P42
[9]
Composition and biological activity of traditional and commercial kava extracts [J].
Côté, CS ;
Kor, C ;
Cohen, J ;
Auclair, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 322 (01) :147-152
[10]
Delgoda Rupika, 2004, Toxicol Rev, V23, P239, DOI 10.2165/00139709-200423040-00004