Zhang Miaogao, Qiu Zhenguo
College of Light Industry and Food Sciences, Academy of Contemporary Agricultural Engineering Innovations, Zhongkai University of Agriculture and Engineering, Guangzhou, China.
Food Nutr Res. 2024 Sep 27;68. doi: 10.29219/fnr.v68.10605. eCollection 2024.
In this study, (-)-epigallocatechin gallate (EGCG) and caffeine extracted from freeze-dried autumn Baiyedancong Oolong tea (FBOT) were orally administered to mice for 7 consecutive days to explore the effects of BOT and its bioactive compounds on the activities and transcription levels of CYP450 enzymes, intestinal effluence transporter P-gp, and renal ingestion Organic Anion Transporters (OATs). Concurrently, EGCG and caffeine enhanced the activities of CYP3A, CYP2E1, and CYP2C37 in the liver of mice, while impairing the transport capabilities of P-gp and OATs. Reduced levels of MDR1 encoding P-gp transcription in the small intestine and renal OAT1 and OAT3 revealed that transcription was involved in the regulation of CYP450, P-gp, and OATs. The reduced transcription level of liver CYP2E1 suggested that CYP2E1 activity may have been elevated due to alternative mechanisms, but not through transcription. The absorption, metabolism, and excretion of drugs may be influenced by the daily consumption or high-dose administration of BOT and its related products, in which EGCG and caffeine may make great contributions.
在本研究中,将从冻干的秋季白叶单枞乌龙茶(FBOT)中提取的(-)-表没食子儿茶素没食子酸酯(EGCG)和咖啡因连续7天口服给予小鼠,以探究FBOT及其生物活性化合物对CYP450酶、肠道流出转运体P-糖蛋白(P-gp)和肾脏摄取有机阴离子转运体(OATs)的活性及转录水平的影响。同时,EGCG和咖啡因增强了小鼠肝脏中CYP3A、CYP2E1和CYP2C37的活性,同时损害了P-gp和OATs的转运能力。小肠中编码P-gp转录的多药耐药蛋白1(MDR1)水平以及肾脏中的OAT1和OAT3水平降低,表明转录参与了对CYP450、P-gp和OATs的调节。肝脏CYP2E1转录水平降低表明,CYP2E1活性可能因其他机制而升高,而非通过转录升高。药物的吸收、代谢和排泄可能会受到FBOT及其相关产品的日常消费或高剂量给药的影响,其中EGCG和咖啡因可能起了很大作用。