In vivo effect of I'm-Yunity on hepatic cytochrome P450 3A4.

Journal of herbal pharmacotherapy Pub Date : 2007-01-01
Jean Paul A Nicandro, Candy Tsourounis, Lynda Frassetto, B Joseph Guglielmo
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Abstract

The inhibition or induction of hepatic cytochrome P450 3A4 (CYP3A4) enzyme associated with herbal medicines such as I'm-Yunity (Coriolus versicolor) can result in clinically significant herb-drug interactions. The active ingredient of I'm-Yunity is believed to be polysaccharopeptide polymer (PSP). Drug interactions between I'm-Yunity and other medications or supplements are yet to be investigated. The objective of this single-treatment, one-period, three-phase, open-labeled study was to evaluate the ability of I'm-Yunity to inhibit or induce CYP3A4 in 12 healthy adult volunteers (8 women and 4 men) aged between 23 and 54 years through the use of a CYP3A4-specific assay, the erythromycin breath test (EBT). EBT measurements are reported as percentage of 14C-Erythromycin metabolized/hr. Participants were given a 14-day supply of I'm-Yunity and instructed to take 1200 mg, three times daily with meals. Comparisons of all subjects' mean CYP3A4 activities were performed with the EBT before and after taking I'm- Yunity. Results revealed a mean EBT change (SD) from baseline of 0.08% (0.56%) 14C-Erythromycin metabolized/hr, which was not significant (p = 0.63). Therefore, 14 days of exposure to I'm-Yunity was not associated with clinically significant CYP3A4 inhibition or induction, suggesting that short-term administration of I'm-Yunity with medications primarily metabolized by CYP3A4 is safe and not expected to be associated with significant herb-drug interactions. However, it is still unknown whether interactions exist between I'm-Yunity and other medications metabolized by other CYP450 isozymes or enzyme/transporter systems.

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I'm-Yunity对肝细胞色素P450 - 3A4的体内影响。
抑制或诱导肝细胞色素P450 3A4 (CYP3A4)酶与草药相关,如I'm-Yunity (corolus versicolor)可导致临床显着的草药相互作用。认为其活性成分为多糖多肽聚合物(PSP)。I'm-Yunity和其他药物或补充剂之间的药物相互作用还有待研究。这项单治疗、一期、三期、开放标记研究的目的是通过使用红霉素呼吸试验(EBT)来评估I'm-Yunity在12名年龄在23至54岁的健康成人志愿者(8名女性和4名男性)中抑制或诱导CYP3A4的能力。EBT测量报告为14c -红霉素代谢/小时百分比。研究人员给参与者提供了为期14天的I'm-Yunity,并指示他们每天三次,每次服用1200毫克,随餐服用。用EBT比较所有受试者服用I'm- Yunity前后的平均CYP3A4活性。结果显示,与基线相比,平均EBT变化(SD)为0.08% (0.56%),14 c -红霉素代谢/小时,差异无统计学意义(p = 0.63)。因此,暴露于I'm-Yunity 14天与临床显著的CYP3A4抑制或诱导无关,这表明I'm-Yunity与主要由CYP3A4代谢的药物的短期服用是安全的,预计不会与显著的草药相互作用相关。然而,I'm-Yunity与其他CYP450同工酶或酶/转运体系统代谢的其他药物之间是否存在相互作用尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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