用相对表达因子估计单udp -葡萄糖醛基转移酶的药物代谢分数

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Tomoyo Honda, Wataru Obuchi, Yumi Nishiya, Takahiro Shibayama, Kengo Watanabe, Nobuaki Watanabe
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引用次数: 0

摘要

与细胞色素p450 (CYPs)不同,由于重组系统和特异性抑制剂中酶水平的信息有限,估计udp -葡萄糖醛酸转移酶(UGT)同工异构体对整体代谢的贡献仍然存在技术困难。采用液相色谱-串联质谱法定量分析UGT在重组系统微粒体(RM)和人肝微粒体(HLM)中的蛋白表达水平,并估算其对重组微粒体的相对表达因子(REF)值,评价UGT底物单UGT酶(fmUGT)对药物代谢的影响。UGT1A1、UGT1A3、UGT1A9、UGT2B4、UGT2B7、UGT2B17的REF值分别为0.228、0.0714、0.0665、0.420、0.118、0.0442。利用这些值和RM中的代谢清除率估算了几种典型UGT底物在HLM中的fmugt。这些值与各种方法估计的报告值相当。该研究提供了关于REF值的有用信息,在评估UGT同种异构体对总代谢清除率的贡献时,促进了对UGT底物fmUGT值的稳健估计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Estimation of fraction of drug metabolism by a single UDP-glucuronosyl transferase enzyme using relative expression factor

Estimation of fraction of drug metabolism by a single UDP-glucuronosyl transferase enzyme using relative expression factor

The estimation of the contributions of UDP-glucuronosyl transferase (UGT) isoforms to the overall metabolism still suffers from technical difficulties due to limited information on enzyme levels in recombinant systems and specific inhibitors, unlike the case for cytochrome P450s (CYPs). The protein expression levels of UGT in both recombinant system microsomes (RM) and human liver microsomes (HLM) were quantified using liquid chromatography-tandem mass spectrometry, and the relative expression factor (REF) value of HLM to recombinant microsomes was estimated to evaluate the fractions of drug metabolism by a single UGT enzyme (fmUGT) of UGT substrates. The REF values of UGT1A1, UGT1A3, UGT1A9, UGT2B4, UGT2B7, and UGT2B17 were 0.228, 0.0714, 0.0665, 0.420, 0.118, and 0.0442, respectively. fmUGTs in HLM were estimated for several typical UGT substrates utilizing these values and metabolic clearances in RM. These values were comparable to the reported values estimated by various methods. This study provided useful information on REF values, which promote a robust estimation of fmUGT values for UGT substrates when evaluating the contribution of UGT isoforms to total metabolic clearance.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
35
审稿时长
6-12 weeks
期刊介绍: Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes: - animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites, - in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man - studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition, - simulation and modeling in drug discovery and development - theoretical treatises - includes themed issues and reviews and exclude manuscripts on - bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation - analytical methods
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