Program in Pharmacology and Experimental Therapeutics, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts, USA.
Clin Pharmacol Ther. 2012 Nov;92(5):651-7. doi: 10.1038/clpt.2012.170. Epub 2012 Oct 10.
Nutrient interactions with prescription drugs are a topic of ongoing basic and clinical research. Pomegranate juice and a 1-g capsule containing pomegranate extract were evaluated in vitro and in vivo as inhibitors of cytochrome P450 2C9 (CYP2C9), with flurbiprofen serving as the index substrate. Fluconazole was the positive control inhibitor. The in vitro 50% inhibitory concentration (IC(50)) values for pomegranate juice and extract were below 1% (vol/vol), with no evidence of mechanism-based (irreversible) inhibition. In clinical studies, flurbiprofen pharmacokinetics were unchanged by pomegranate juice or extract as compared to a low-polyphenol placebo control beverage. However, fluconazole significantly reduced the oral clearance of flurbiprofen. Despite inhibition of CYP2C9 in vitro, pomegranate juice and extract had no effect on CYP2C9 activity in human subjects, and can be consumed by patients taking CYP2C9 substrate drugs with negligible risk of a pharmacokinetic interaction.
营养物质与处方药的相互作用是一个持续的基础和临床研究课题。石榴汁和含有石榴提取物的 1 克胶囊被评估为细胞色素 P450 2C9(CYP2C9)的抑制剂,氟比洛芬作为指数底物。氟康唑是阳性对照抑制剂。石榴汁和提取物的体外 50%抑制浓度(IC50)值低于 1%(体积/体积),没有证据表明存在基于机制的(不可逆)抑制。在临床研究中,与低多酚安慰剂对照饮料相比,石榴汁或提取物对氟比洛芬的药代动力学没有影响。然而,氟康唑显著降低了氟比洛芬的口服清除率。尽管体外抑制了 CYP2C9,但石榴汁和提取物对人类 CYP2C9 活性没有影响,并且可以被服用 CYP2C9 底物药物的患者食用,几乎没有发生药代动力学相互作用的风险。