非索非那定
葡萄柚汁
有机阴离子转运多肽
化学
药理学
药代动力学
硫酸雌酮
Abcg2型
运输机
生物化学
雌酮
ATP结合盒运输机
医学
激素
基因
作者
Tokio Morita,Takeshi Akiyoshi,Toshiaki Tsuchitani,Hiroki Kataoka,Naoya Araki,Kodai Yajima,Kazuhiro Katayama,Ayuko Imaoka,Hisakazu Ohtani
标识
DOI:10.1021/acs.jafc.2c00065
摘要
Organic anion-transporting polypeptide (OATP) 1A2 and OATP2B1 mediate the intestinal absorption of drugs. This study aimed to identify fruit juices or fruit juice components that inhibit OATPs and assess the risk of associated food–drug interactions. Inhibitory potency was assessed by examining the uptake of [ 3 H]estrone 3-sulfate and [ 3 H]fexofenadine into HEK293 cells expressing OATP1A2 or OATP2B1. In vivo experiments were conducted using mice to evaluate the effects of cranberry juice on the pharmacokinetics of orally administered fexofenadine. Of eight examined fruit juices, cranberry juice inhibited the functions of both OATPs most potently. Avicularin, a component of cranberry juice, was identified as a novel OATP inhibitor. It exhibited IC 50 values of 9.0 and 37 μM for the inhibition of estrone 3-sulfate uptake mediated by OATP1A2 and OATP2B1, respectively. A pharmacokinetic experiment revealed that fexofenadine exposure was significantly reduced (by 50%) by cranberry juice. Cranberry juice may cause drug interactions with OATP substrates.
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