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Identification of the active compounds and significant pathways of yinchenhao decoction based on network pharmacology

机译:基于网络药理学鉴定银chen蒿汤的活性成分及重要途径

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摘要

Yinchenhao decoction (YCHD) is a traditional Chinese medicine formulation, which has been widely used for the treatment of jaundice for 2,000 years. Currently, YCHD is used to treat various liver disorders and metabolic diseases, however its chemical/pharmacologic profiles remain to be elucidated. The present study identified the active compounds and significant pathways of YCHD based on network pharmacology. All of the chemical ingredients of YCHD were retrieved from the Traditional Chinese Medicine Systems Pharmacology database. Absorption, distribution, metabolism and excretion screening with oral bioavailability (OB) screening, drug-likeness (DL) and intestinal epithelial permeability (Caco-2) evaluation were applied to discover the bioactive compounds in YCHD. Following this, target prediction, pathway identification and network construction were employed to clarify the mechanism of action of YCHD. Following OB screening, and evaluation of DL and Caco-2, 34 compounds in YCHD were identified as potential active ingredients, of which 30 compounds were associated with 217 protein targets. A total of 31 significant pathways were obtained by performing enrichment analyses of 217 proteins using the JEPETTO 3.x plugin, and 16 classes of gene-associated diseases were revealed by performing enrichment analyses using Database for Annotation, Visualization and Integrated Discovery v6.7. The present study identified potential active compounds and significant pathways in YCHD. In addition, the mechanism of action of YCHD in the treatment of various diseases through multiple pathways was clarified.
机译:茵陈好汤(YCHD)是一种中药制剂,已被广泛用于治疗黄疸2000年。目前,YCHD用于治疗各种肝脏疾病和代谢性疾病,但是其化学/药理作用仍有待阐明。本研究基于网络药理学鉴定了YCHD的活性化合物和重要途径。 YCHD的所有化学成分均从中药系统药理数据库检索。通过口服生物利用度(OB)筛选,药物相似性(DL)和肠上皮渗透性(Caco-2)评估吸收,分布,代谢和排泄物,以发现YCHD中的生物活性化合物。此后,通过目标预测,途径识别和网络构建来阐明YCHD的作用机理。经过OB筛选和DL和Caco-2评估,鉴定出YCHD中的34种化合物为潜在的活性成分,其中30种化合物与217个蛋白质靶标相关。通过使用JEPETTO 3.x插件对217种蛋白质进行富集分析,总共获得了31条重要途径,并且通过使用注释,可视化和集成发现v6.7数据库进行了富集分析,揭示了16类基因相关疾病。本研究确定了潜在的活性化合物和YCHD中的重要途径。此外,阐明了YCHD通过多种途径治疗各种疾病的作用机理。

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