...
首页> 外文期刊>Pharmacognosy magazine >Studying the Inhibitory Effect of Quercetin and Thymoquinone on Human Cytochrome P450 Enzyme Activities
【24h】

Studying the Inhibitory Effect of Quercetin and Thymoquinone on Human Cytochrome P450 Enzyme Activities

机译:槲皮素和胸腺醌对人细胞色素P450酶活性的抑制作用研究

获取原文
           

摘要

Background: Quercetin (QR) and thymoquinone (TQ) are herbal remedies that are currently extensively used by the general population to prevent and treat various chronic conditions. Therefore, investigating the potential of pharmacokinetic interactions caused by the concomitant use of these herbal remedies and conventional medicine is warranted to ensure patient safety. Purpose of the Study: This study was conducted to determine the inhibitory effect of QR and TQ, two commonly used remedies, on the activities of selected cytochrome P450 (CYP) enzymes that play an important role in drug metabolism and/or toxicology. Materials and Methods: The in vitro studies were conducted using fluorescence-based high throughput assays using human c-DNA baculovirus expressed CYP enzymes. For measuring CYP2E1 activity, a validated High-performance liquid chromatography (HPLC) assay was utilized to measure the formation of 6-hydroxychlorzoxazone. Results: The obtained half-maximum inhibitory concentration values with known positive control inhibitors of this study were comparable to the published values indicating accurate experimental techniques. Although QR did not show any significant effect on CYP1A2 and CYP2E1, it exhibited a strong inhibitory effect against CYP2D6 and a moderate effect against CYP2C19 and CYP3A4. On the other hand, TQ demonstrated a strong and a moderate inhibitory effect against CYP3A4 and CYP2C19, respectively. Conclusions: The findings of this study may indicate that consumption of QR or TQ, in the form of food or dietary supplements, with drugs that are metabolized by CYP2C19, CYP2D6, or CYP3A4 may cause significant herb-drug interactions. SUMMARY Neither QR nor TQ has any significant inhibitory effect on the activity of CYP1A2 or CYP2E1 enzymes Both QR and TQ have a moderate to strong inhibitory effect on CYP3A4 activity QR has a moderate inhibitory effect on CYP2C19 and a strong inhibitory effect on CYP2D6 Both QR and TQ are moderate inhibitors of the CYP2C9 activity. Abbreviations used: ABT: Aminobenztriazole, BZF: 7,8 Benzoflavone, CYP: Cytochrome P450, GB: Gingko Biloba, IC50: Half-maximum inhibitory concentration, KTZ: Ketoconazole, QND: Quinidine, QR: Quercetin, TCP: Tranylcypromine, TQ: Thymoquinone.
机译:背景:槲皮素(QR)和胸腺醌(TQ)是草药,目前已被普通人群广泛用于预防和治疗各种慢性病。因此,有必要调查因同时使用这些草药和常规药物而引起的药代动力学相互作用的潜力,以确保患者安全。研究目的:本研究旨在确定QR和TQ这两种常用疗法对选定的细胞色素P450(CYP)酶的活性的抑制作用,这些酶在药物代谢和/或毒理学中起重要作用。材料与方法:体外研究是使用基于荧光的高通量测定法进行的,其中使用了人类c-DNA杆状病毒表达的CYP酶。为了测量CYP2E1活性,采用了经过验证的高效液相色谱(HPLC)分析法来测量6-羟基氯唑沙宗的形成。结果:使用本研究的已知阳性对照抑制剂获得的半数最大抑菌浓度值与表明准确的实验技术的公开值相当。尽管QR对CYP1A2和CYP2E1没有显示任何显着作用,但它对CYP2D6表现出强抑制作用,对CYP2C19和CYP3A4表现出中等作用。另一方面,TQ分别显示出对CYP3A4和CYP2C19的强抑制作用。结论:本研究的发现可能表明,以食物或膳食补充剂的形式通过被CYP2C19,CYP2D6或CYP3A4代谢的药物摄入QR或TQ可能引起显着的草药-药物相互作用。总结QR和TQ均未对CYP1A2或CYP2E1酶的活性产生任何明显的抑制作用QR和TQ均对CYP3A4的活性具有中度至强的抑制作用QR对CYP2C19的抑制作用中等且对CYP2D6的抑制作用TQ是CYP2C9活性的中度抑制剂。使用的缩写:ABT:氨基苯并三唑,BZF:7,8苯并黄酮,CYP:细胞色素P450,GB:银杏叶,IC 50 :半最大抑制浓度,KTZ:酮康唑,QND:奎尼丁,QR:槲皮素,TCP:Tranylcypromine,TQ:胸醌。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号