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香料成分对体外P-糖蛋白介导的转运和CYP3A4介导的代谢的影响。

Effects of spice constituents on P-glycoprotein-mediated transport and CYP3A4-mediated metabolism in vitro.

作者信息

Zhang Wenxia, Lim Lee-Yong

机构信息

Department of Pharmacy, National University of Singapore, Singapore.

出版信息

Drug Metab Dispos. 2008 Jul;36(7):1283-90. doi: 10.1124/dmd.107.019737. Epub 2008 Apr 2.

Abstract

The effects of eight components from six commonly consumed spices on P-glycoprotein (P-gp) transport and CYP3A4 metabolism were evaluated in vitro. P-gp-mediated [(3)H]digoxin fluxes across the L-MDR1 (LLC-PK1 cells transfected with human MDR1 gene) and Caco-2 (human colon carcinoma) cell monolayers showed a marked asymmetry compared with that in the LLC-PK1 (porcine kidney epithelial cells) cell monolayers. Curcumin (from turmeric) at 30 to 60 microM and 6-gingerol (from ginger) at 100 to 500 microM were observed to inhibit P-gp-mediated [(3)H]digoxin transport in L-MDR1 and Caco-2 cells. Effects of spices on midazolam (MDZ) 1'-hydroxylation and 4-hydroxylation of CYP3A4 activity were determined in pooled human liver microsomes (HLM). The following IC(50) values for effects of spices on MDZ 1'-hydroxylation in HLM were obtained: 29 microM for curcumin, 1.17 mM for allyl methyl disulfide (AMD) (from Chinese chive), 1.02 mM for 1,8-cineole (from coriander), and 1.28 mM for beta-caryophyllene (from curry leaf). CYP3A4-mediated 4-hydroxylation of MDZ was inhibited by curcumin at 30, 45, and 60 microM (4-hydroxy-MDZ formation was decreased to 52, 30, and 29%, respectively, compared with control), by 6-gingerol at 60, 100, and 500 microM (71, 68, and 38%), by AMD at 1 and 4 mM (29 and 14%), by d-limonene (from coriander) at 4 mM (65%), by 1,8-cineole at 0.5, 1, and 4 mM (74, 64, and 59%), and by citral (from lemongrass) at 1 mM (59%). Among the spices that showed inhibitory effect on MDZ metabolism in HLM, only AMD showed a preincubation time-dependent inhibitory effect on MDZ metabolism in HLM, suggesting the AMD as an irreversible CYP3A4 inhibitor.

摘要

在体外评估了六种常用香料中的八种成分对P-糖蛋白(P-gp)转运和CYP3A4代谢的影响。与LLC-PK1(猪肾上皮细胞)单层细胞相比,P-gp介导的[³H]地高辛跨L-MDR1(转染人MDR1基因的LLC-PK1细胞)和Caco-2(人结肠癌)单层细胞的通量显示出明显的不对称性。观察到30至60微摩尔的姜黄素(来自姜黄)和100至500微摩尔的6-姜酚(来自生姜)可抑制L-MDR1和Caco-2细胞中P-gp介导的[³H]地高辛转运。在人肝微粒体(HLM)中测定了香料对咪达唑仑(MDZ)1'-羟基化和CYP3A4活性4-羟基化的影响。获得了以下香料对HLM中MDZ 1'-羟基化影响的IC₅₀值:姜黄素为29微摩尔,烯丙基甲基二硫化物(AMD,来自韭菜)为1.17毫摩尔,1,8-桉叶素(来自香菜)为1.02毫摩尔,β-石竹烯(来自咖喱叶)为1.28毫摩尔。30、45和60微摩尔的姜黄素抑制了CYP3A4介导的MDZ 4-羟基化(与对照相比,4-羟基-MDZ的形成分别降至52%、30%和29%),60、100和500微摩尔的6-姜酚(分别为71%、68%和38%),1和4毫摩尔的AMD(分别为29%和14%),4毫摩尔的d-柠檬烯(来自香菜)(65%),0.5、1和4毫摩尔的1,8-桉叶素(分别为74%、64%和59%),以及1毫摩尔的柠檬醛(来自柠檬草)(59%)。在对HLM中MDZ代谢表现出抑制作用的香料中,只有AMD对HLM中MDZ代谢表现出预孵育时间依赖性抑制作用,表明AMD是一种不可逆的CYP3A4抑制剂。

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