Institute of Clinical Pharmacology, Central South University, 110 Xiang-Ya Road, Changsha, Hunan 410078, China.
J Ethnopharmacol. 2010 Oct 28;132(1):213-8. doi: 10.1016/j.jep.2010.08.011. Epub 2010 Aug 17.
Liu wei di huang wan (LDW), a well-known traditional Chinese medicine, is frequently combined with other prescription or non-prescription drugs in China.
This study was designed to investigate the effects of LDW on the activities of CYP1A2, CYP2A6, N-acetyltransferase 2 (NAT2) and xanthine oxidase (XO) in healthy subjects, using caffeine as a probe drug.
Twelve unrelated healthy males were enrolled in a single-blind, randomized, placebo-controlled, two-phase crossover study. Placebo or LDW (12 pills, 0.2 g/pill, twice daily) was given to each participant for 14 continuous days with a wash-out period of 2 weeks. A dose of 100 mg caffeine was given afterwards to test the activities of drug-metabolizing enzymes of interest.
Compared to placebo, LDW significantly induced the CYP1A2 activity, as determined by an increase in the ratio of (AFMU+1U+1X)/17U and the formation of 17X and 1X after taking caffeine. Interestingly, LDW significantly decreased the ratio of 17U/(17U+17X+1X+1U+AFMU) and the formation of 17U (CYP2A6-mediated) (by 39.2%; 95%CI: 23.1-55.3%; P=0.026), and decreased the ratio of AFMU/(AFMU+1U+1X) and the formation of AFMU (NAT2-catalyzed) (by 26.2%; 95%CI: 9.2-61.6%; P=0.038), suggesting a marked inhibition of CYP2A6 and NAT2, respectively.
LDW can induce CYP1A2 and suppress CYP2A6 and NAT2 activities, and affect caffeine metabolism in vivo.
六味地黄丸(LDW)是一种著名的中药,在中国常与其他处方药或非处方药联合使用。
本研究旨在使用咖啡因作为探针药物,研究 LDW 对健康受试者 CYP1A2、CYP2A6、N-乙酰基转移酶 2(NAT2)和黄嘌呤氧化酶(XO)活性的影响。
12 名无关的健康男性参加了一项单盲、随机、安慰剂对照、两周期交叉研究。每位参与者连续 14 天服用安慰剂或 LDW(12 片,0.2 g/片,每日 2 次),2 周洗脱期后给予 100mg 咖啡因剂量以测试所关注的药物代谢酶活性。
与安慰剂相比,LDW 显著诱导 CYP1A2 活性,表现在服用咖啡因后(AFMU+1U+1X)/17U 比值增加,17X 和 1X 的生成增加。有趣的是,LDW 显著降低了 17U/(17U+17X+1X+1U+AFMU)比值和 17U 的生成(CYP2A6 介导)(减少 39.2%;95%CI:23.1-55.3%;P=0.026),并降低了 AFMU/(AFMU+1U+1X)比值和 AFMU 的生成(NAT2 催化)(减少 26.2%;95%CI:9.2-61.6%;P=0.038),分别表明 CYP2A6 和 NAT2 的显著抑制。
LDW 可诱导 CYP1A2,抑制 CYP2A6 和 NAT2 活性,影响体内咖啡因代谢。