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六味地黄丸是一种著名的中药,可诱导人肝 CYP1A2 的表达,同时抑制 CYP2A6 和 N-乙酰基转移酶 2 的活性。

Liu wei di huang wan, a well-known traditional Chinese medicine, induces CYP1A2 while suppressing CYP2A6 and N-acetyltransferase 2 activities in man.

机构信息

Institute of Clinical Pharmacology, Central South University, 110 Xiang-Ya Road, Changsha, Hunan 410078, China.

出版信息

J Ethnopharmacol. 2010 Oct 28;132(1):213-8. doi: 10.1016/j.jep.2010.08.011. Epub 2010 Aug 17.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Liu wei di huang wan (LDW), a well-known traditional Chinese medicine, is frequently combined with other prescription or non-prescription drugs in China.

AIM OF THE STUDY

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.

MATERIALS AND METHODS

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.

RESULTS

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.

CONCLUSIONS

LDW can induce CYP1A2 and suppress CYP2A6 and NAT2 activities, and affect caffeine metabolism in vivo.

摘要

民族药理学相关性

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。

研究目的

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。

材料和方法

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。

结果

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。

结论

LDW 可诱导 CYP1A2,抑制 CYP2A6 和 NAT2 活性,影响体内咖啡因代谢。

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