Oh Hyun-A, Lee Hyunbeom, Kim Donghak, Jung Byung Hwa
Molecular Recognition Research Center, Korea Institute of Science and Technology, Seoul 136-791, Republic of Korea; Department of Biological Sciences, Konkuk University, Seoul 143-701, Republic of Korea.
Molecular Recognition Research Center, Korea Institute of Science and Technology, Seoul 136-791, Republic of Korea.
Anal Biochem. 2017 Feb 15;519:71-83. doi: 10.1016/j.ab.2016.12.015. Epub 2016 Dec 20.
As drug interactions with cytochrome P450 enzymes become increasingly important in the field of drug discovery, a high-throughput screening method for analysing the effects of a drug is needed. We have developed a simple and rapid simultaneous analytical method using a cocktail approach for measuring the activities of seven cytochrome P450 enzymes (CYP1A2, CYP2A6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4). Human liver microsomes were used as a source for the seven cytochrome P450 enzymes, and a gas chromatography-mass spectrometry (GC-MS) was used for analysing their activities. Kinetic studies and inhibition assays of CYP enzymes were performed using known substrates and inhibitors for validating and comparing the reaction rates and time-dependent activities between methods using each substrate versus a method using a cocktail solution. The optimized cocktail method was successfully applied to evaluate the effects of the decoction of Socheongryong-tang (SCRT) on cytochrome P450 enzymes. Our cocktail method provides a simultaneous high-throughput activity assay using GC-MS for the first time. This method is applicable for analysing the drug interactions of various plant-derived mixtures.
随着药物与细胞色素P450酶的相互作用在药物发现领域变得越来越重要,需要一种用于分析药物作用的高通量筛选方法。我们开发了一种简单快速的同时分析方法,采用鸡尾酒法来测量七种细胞色素P450酶(CYP1A2、CYP2A6、CYP2C9、CYP2C19、CYP2D6、CYP2E1和CYP3A4)的活性。用人肝微粒体作为这七种细胞色素P450酶的来源,并使用气相色谱-质谱联用仪(GC-MS)分析它们的活性。使用已知的底物和抑制剂进行CYP酶的动力学研究和抑制试验,以验证和比较使用每种底物的方法与使用混合溶液的方法之间的反应速率和时间依赖性活性。优化后的鸡尾酒法成功应用于评价小青龙汤(SCRT)水煎剂对细胞色素P450酶的影响。我们的鸡尾酒法首次提供了一种使用GC-MS的同时高通量活性测定方法。该方法适用于分析各种植物源混合物的药物相互作用。