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西洋参(Panax quinquefolius)对2期酶和抗氧化途径的潜在差异诱导作用。

Possible differential induction of phase 2 enzyme and antioxidant pathways by american ginseng, Panax quinquefolius.

作者信息

Lee Lawrence S, Wise Stephen D, Chan Clark, Parsons Teresa L, Flexner Charles, Lietman Paul S

机构信息

Division of Clinical Pharmacology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

J Clin Pharmacol. 2008 May;48(5):599-609. doi: 10.1177/0091270008314252. Epub 2008 Mar 4.

Abstract

Human immunodeficiency virus (HIV)-infected patients often take herbal medicines, which may interact with antiretrovirals. American ginseng induces phase 2 and antioxidant enzymes in vitro and might increase the clearance of zidovudine and/or enhance antioxidant activity. Ten healthy volunteers received 300 mg of zidovudine orally before and after 2 weeks of treatment with a ginsenoside-enriched American ginseng extract 200 mg twice daily. This ginseng extract induced the phase 2 enzyme quinone reductase with an average concentration of doubling of enzyme activity of 190 microg/mL. Total ginsenoside content was 8.5 +/- 0.5%. Pharmacokinetic profiles of zidovudine and oxidative stress marker concentrations were measured post-zidovudine dose. American ginseng does not significantly affect the formation clearance of zidovudine to its glucuronide (ratio post- to pre-American ginseng = 1.17; 90% confidence interval: 0.95-1.45; P = .21), total clearance (ratio = 0.97; 0.82-1.14; P = .70), or plasma zidovudine AUC0-8 (ratio = 1.03; 0.87-1.21; P = .77). Oxidative stress biomarkers are reduced post-American ginseng (F2-isoprostane ratio = 0.79; 0.72-0.86; P < .001; 8-hydroxy-deoxyguanosine ratio = 0.74; 0.59-0.92; P = .02). Two weeks of American ginseng does not alter zidovudine pharmacokinetics but reduces oxidative stress markers.

摘要

感染人类免疫缺陷病毒(HIV)的患者常服用草药,这些草药可能与抗逆转录病毒药物发生相互作用。西洋参在体外可诱导Ⅱ相酶和抗氧化酶,可能会增加齐多夫定的清除率和/或增强抗氧化活性。10名健康志愿者在每日两次服用200mg富含人参皂苷的西洋参提取物治疗2周前后,口服300mg齐多夫定。这种人参提取物诱导Ⅱ相酶醌还原酶,酶活性平均浓度加倍至190μg/mL。总人参皂苷含量为8.5±0.5%。在服用齐多夫定后测量其药代动力学曲线以及氧化应激标志物浓度。西洋参对齐多夫定转化为其葡糖醛酸苷的生成清除率(西洋参治疗后与治疗前的比值=1.17;90%置信区间:0.95-1.45;P=0.21)、总清除率(比值=0.97;0.82-1.14;P=0.70)或血浆齐多夫定AUC0-8(比值=1.03;0.87-1.21;P=0.77)均无显著影响。服用西洋参后氧化应激生物标志物减少(F2-异前列腺素比值=0.79;0.72-0.86;P<0.001;8-羟基脱氧鸟苷比值=0.74;0.59-0.92;P=0.02)。两周的西洋参治疗未改变齐多夫定的药代动力学,但降低了氧化应激标志物水平。

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