咖啡因和甲基利比里亚的人体药代动力学相互作用研究

Goutam Mondal, Yan-hong Wang, Ryan Yates, R. Bloomer, M. Butawan
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引用次数: 2

摘要

简介:甲基赖氨酸和茶泌酸是分别存在于各种Coffea和Camellia assamica var.kucha的叶片中的甲基尿酸盐。我们之前已经证明,甲基黄嘌呤咖啡因增加了人类的口服生物利用度。方法:因此,我们在人类中进行了一项双盲、安慰剂对照的药物代谢动力学研究,以确定甲基利比里亚与咖啡因或茶泌碱的药代动力学相互作用潜力。受试者采用随机、双盲、交叉设计接受口服剂量的甲基利比里亚、咖啡因、甲基利比里亚加咖啡因或甲基利比里亚加茶泌物。使用UPLC-MS/MS分析血液样本。结果:甲基利比里亚呈现线性药代动力学,不受咖啡因或茶分泌共同给药的影响。然而,甲基利比里亚联合给药导致咖啡因的口服清除率降低(41.9±19.5对17.1±7.80 L/hr),半衰期增加(7.2±5.6对15±5.8小时)。甲基利比里亚对咖啡因的最大浓度(440±140 vs.458±93.5 ng/mL)或口服分布体积(351±148 vs.316±76.4 L)没有影响。在本文中,我们发现甲基利比里亚在没有相互作用的情况下改变了咖啡因的药代动力学,这表明咖啡因可能与不同的甲基尿酸盐独特地相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Caffeine and Methylliberine: A Human Pharmacokinetic Interaction Study
Introduction: Methylliberine and theacrine are methylurates found in the leaves of various Coffea species and Camellia assamica var. kucha, respectively. We previously demonstrated that the methylxanthine caffeine increased theacrine’s oral bioavailability in humans. Methods:  Consequently, we conducted a double-blind, placebo-controlled pharmacokinetic study in humans administered methylliberine, theacrine, and caffeine to determine methylliberine’s pharmacokinetic interaction potential with either caffeine or theacrine. Subjects received an oral dose of either methylliberine, caffeine, methylliberine plus caffeine, or methylliberine plus theacrine using a randomized, double-blind, crossover design. Blood samples were analyzed using UPLC-MS/MS.    Results: Methylliberine exhibited linear pharmacokinetics that were unaffected by co-administration of either caffeine or theacrine. However, methylliberine co-administration resulted in decreased oral clearance (41.9 ± 19.5 vs. 17.1 ± 7.80 L/hr) and increased half-life (7.2 ± 5.6 versus 15 ± 5.8 hrs) of caffeine. Methylliberine had no impact on caffeine’s maximum concentration (440 ± 140 vs. 458 ± 93.5 ng/mL) or oral volume of distribution (351 ± 148 vs. 316 ± 76.4 L). Conclusions: We previously demonstrated theacrine bioavailability was enhanced by caffeine, however, caffeine pharmacokinetics were unaffected by theacrine. Herein, we found that methylliberine altered caffeine pharmacokinetics without a reciprocal interaction, which suggests caffeine may interact uniquely with different methylurates.
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