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首页> 外文期刊>Pharmacognosy magazine >Inhibition of Cytochrome P450 (CYP3A4) Activity by Extracts from 57 Plants Used in Traditional Chinese Medicine (TCM)
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Inhibition of Cytochrome P450 (CYP3A4) Activity by Extracts from 57 Plants Used in Traditional Chinese Medicine (TCM)

机译:来自57种中药(TCM)的植物提取物对细胞色素P450(CYP3A4)活性的抑制作用

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Background: Herbal medicine is widely used all over the world for treating various health disorders. It is employed either alone or in combination with synthetic drugs or plants to be more effective. Objective: The assessment of the effect of both water and methanol extracts of 57 widely used plants from Traditional Chinese Medicine (TCM) against the main phase I metabolizing enzyme CYP3A4 in vitro for the first time. Materials and Methods: The inhibition of cytochrome P450 activity was evaluated using a luminescence assay. The principal component analysis (PCA) was used to correlate the inhibitory activity with the main secondary metabolites present in the plant extracts. Molecular modeling studies on CYP3A4 (PDB ID 4NY4) were carried out with 38 major compounds present in the most active plant extracts to validate the observed inhibitory effect. Results: Aqueous extracts of Acacia catechu , Andrographis paniculata , Arctium lappa , Areca catechu , Bupleurum marginatum , Chrysanthemum indicum , Dysosma versipellis , and Spatholobus suberectus inhibited CYP3A4 is more than 85% (at a dose of 100 μg/mL). The corresponding methanol extracts of A. catechu , A. paniculata , A. catechu , Mahonia bealei , and Sanguisorba officinalis inhibited the enzyme by more than 50%. Molecular modeling studies revealed that two polyphenols, namely hesperidin and rutin, revealed the highest fitting scores in the active sites of the CYP3A4 with binding energies equal to -74.09 and -71.34 kcal/mol, respectively. Conclusion: These results provide evidence that many TCM plants can inhibit CYP3A4, which might cause a potential interference with the metabolism of other concomitantly administered herbs or drugs. SUMMARY In this study, the inhibitory activity of the aqueous and methanol extracts of 57 widely used plants from Traditional Chinese Medicine (TCM) against the main phase I metabolizing enzyme CYP3A4 was tested in vitro for the first time. Aqueous extracts of Acacia catechu , Andrographis paniculata , Arctium lappa , Areca catechu , Bupleurum marginatum , Dysosma versipellis , and Spatholobus suberectus inhibited CYP3A4 by more than 85% (at a dose of 100 μg/mL). The activity could be attributed to the presence of polyphenolics as revealed from the multivariate chemometric analysis and molecular modeling study. These results provide evidence that many TCM plants can inhibit CYP3A4, which might cause a potential interference with the metabolism of other concomitantly administered herbs or drugs. Abbreviation used: CHARMm: Chemistry at HARvard Macromolecular Mechanics, CYP: Cytochrome P450, DMSO: Dimethyl Sulfoxide, PCA: Principal Component Analysis, PDB: Protein Data Bank, TCM: Traditional Chinese Medicine
机译:背景:草药在世界范围内广泛用于治疗各种健康疾病。它可以单独使用,也可以与合成药物或植物结合使用,以更有效。目的:首次评估57种中药材(TCM)广泛使用的植物的水和甲醇提取物对主要I相代谢酶CYP3A4的体外作用。材料和方法:使用发光测定法评估细胞色素P450活性的抑制。主成分分析(PCA)用于将抑制活性与植物提取物中存在的主要次要代谢产物相关联。对CYP3A4(PDB ID 4NY4)进行了分子建模研究,研究了活性最高的植物提取物中存在的38种主要化合物,以验证所观察到的抑制作用。结果:相思树,穿心莲,牛t子,槟榔,柴胡,菊花,印度硬皮草和百里香对水生CYP3A4的抑制作用是CYP3A4抑制率超过85%(剂量为100μg/ mL)。相应的A. catechu,A。paniculata,A。catechu,Mahonia bealei和Sanguisorba officinalis的甲醇提取物对该酶的抑制作用超过50%。分子模型研究表明,两种多酚,橙皮苷和芦丁,在CYP3A4活性位点的结合能分别为-74.09和-71.34 kcal / mol,显示出最高的拟合得分。结论:这些结果提供了证据,表明许多中药植物都可以抑制CYP3A4,这可能对其他同时给药的草药或药物的代谢产生潜在的干扰。概述在本研究中,首次在体外测试了57种来自中药的广泛使用的植物的水提取物和甲醇提取物对主要I相代谢酶CYP3A4的抑制活性。刺槐相思,穿心莲,牛,子,槟榔,柴胡,百事香和鸡血藤的水提取物对CYP3A4的抑制作用超过85%(剂量为100μg/ mL)。多元化学计量分析和分子建模研究表明,该活性可能归因于多酚的存在。这些结果提供了证据,表明许多中药植物都可以抑制CYP3A4,这可能会对其他同时给药的草药或药物的代谢产生潜在的干扰。所用缩写:CHARMm:哈佛大分子化学专业,CYP:细胞色素P450,DMSO:二甲基亚砜,PCA:主成分分析,PDB:蛋白质数据库,中药:中药

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