大建中汤(TU-100)在体内饮食模型中改变了小鼠的肝和肠道药物代谢酶:性别和停药的影响。

Daikenchuto (TU-100) alters murine hepatic and intestinal drug metabolizing enzymes in an in vivo dietary model: effects of gender and withdrawal.

机构信息

Department of Medicine, Knapp Center for Biomedical Center, The University of Chicago, Chicago, Illinois.

Tsumura Research Laboratories, Tsumura & Co., Ami, Ibaraki, Japan.

出版信息

Pharmacol Res Perspect. 2017 Oct;5(5). doi: 10.1002/prp2.361.

Abstract

Herbal medicines and natural products used for maintenance of health or treatment of diseases have many biological effects, including altering the pharmacokinetics and metabolism of other medications. Daikenchuto (TU-100), an aqueous extract of ginger, ginseng, and Japanese green pepper fruit, is a commonly prescribed Kampo (Japanese herbal medicine) for postoperative ileus or bloating. The effects of TU-100 on drug metabolism have not been investigated. In this study, we analyzed the effect of TU-100 on expression of key drug-metabolizing enzymes (DMEs) and drug transporters (DTs) in murine liver and gastrointestinal tract using a dietary model. Liver, jejunum, and proximal colon were analyzed for phase I and II DMEs and DT mRNA expression by reverse transcription (RT) first by nonquantitative and followed by quantitative polymerase chain reaction (PCR) and protein expression. Liver, jejunum, and proximal colon expressed some identical but also unique DMEs and DTs. TU-100 increased the greatest changes in cytochrome (Cyp) 2b10 and Cyp3a11 and Mdr1a. Basal and TU-100 stimulated levels of DME and DT expression were gender-dependent, dose-dependent and reversible after cessation of TU-100 supplementation, except for some changes in the intestine. Quantitative Western blot analysis of protein extracts confirmed the quantitative PCR results.

摘要

草药和天然产品用于保持健康或治疗疾病有许多生物效应,包括改变其他药物的药代动力学和代谢。大建中汤(TU-100),一种生姜、人参和日本青椒果实的水提取物,是一种常用于术后肠麻痹或腹胀的常用汉方药。TU-100 对药物代谢的影响尚未被研究。在这项研究中,我们使用膳食模型分析了 TU-100 对鼠肝和胃肠道中关键药物代谢酶(DME)和药物转运蛋白(DT)表达的影响。通过逆转录(RT)首先进行非定量分析,然后进行定量聚合酶链反应(PCR)和蛋白表达分析,对肝、空肠和近端结肠进行 I 相和 II 相 DME 和 DT mRNA 表达分析。肝、空肠和近端结肠表达了一些相同但也独特的 DME 和 DTs。TU-100 增加了细胞色素(Cyp)2b10 和 Cyp3a11 和 Mdr1a 的最大变化。DME 和 DT 表达的基础水平和 TU-100 刺激水平在性别、剂量和 TU-100 补充停止后是可逆的,除了肠道中的一些变化。蛋白提取物的定量 Western blot 分析证实了定量 PCR 结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8e6/5625165/416a5dee6968/PRP2-5-e00361-g001.jpg

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