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鉴定口服当归龙荟丸后产生的代谢产物及其潜在的药理性质的网络药理学分析。

Identification of the metabolites produced following Maxim oral administration and a network pharmacology-based analysis of their potential pharmacological properties.

机构信息

Department of Pharmacy, Yinan People's Hospital, Yinan, Shandong, China.

Guangdong Yi Fang Pharmaceutical Co., Ltd, Foshan, China.

出版信息

Xenobiotica. 2021 Jun;51(6):680-688. doi: 10.1080/00498254.2021.1907473. Epub 2021 Apr 7.

DOI:10.1080/00498254.2021.1907473
PMID:33779496
Abstract
  1. Maxim is a traditional herbal medicine that has been used to treat cancer, abdominal distension, hepatic cirrhosis, and inflammatory diseases. How Maxim is metabolised and the mechanistic basis for its pharmacological activity remain to be defined.2. This study was designed to clarify the metabolism of Maxim and to explore the mechanistic basis for its pharmacological activity.3. In the present study, 51 metabolites were identified via mass spectrometry in samples of bile, urine, and faeces from Wistar rats. Metabolites were mainly formed by glucuronidation, sulphation, methylation, and amino acid conjugation.4. Tectoridin, tectorigenin, irigenin, iristectorigenin A, iristectorigenin B, and 6-hydroxygenistein were identified as potentially be bioactive candidate metabolites for which 36 putative targets and 90 interactions were detected through a network pharmacology analysis. Gene set enrichment analyses and compound-disease networks revealed the targets of these metabolites to regulate important proteins associated with cancer as well as cardiovascular, urogenital, and digestive system diseases.5. Molecular docking confirmed the interactions of these six candidate bioactive metabolites with carbonic anhydrase IV, VII, and XII.6. Overall, these data offer new insights into the metabolism and pharmacological activity of Maxim .
摘要
  1. 麻叶千里光为菊科千里光属植物,民间用于治疗癌症、腹胀、肝硬化和炎症性疾病等。但其代谢过程和药理作用机制尚不清楚。

  2. 本研究旨在阐明麻叶千里光的代谢途径,并探讨其药理作用机制。

  3. 本研究采用液质联用技术,从 Wistar 大鼠胆汁、尿液和粪便中共鉴定出 51 个代谢产物,主要通过葡萄糖醛酸化、硫酸化、甲基化和氨基酸结合等方式代谢。

  4. 通过网络药理学分析,鉴定出 6 个可能具有生物活性的候选代谢产物,即蒙花苷、刺槐素、染料木素、鸢尾黄素 A、鸢尾黄素 B 和 6-羟基大豆苷,共预测到 36 个潜在靶标和 90 个相互作用。基因集富集分析和化合物-疾病网络揭示了这些代谢产物的作用靶点可调控与癌症以及心血管、泌尿生殖和消化系统疾病相关的重要蛋白。

  5. 分子对接实验进一步验证了这 6 个候选生物活性代谢产物与碳酸酐酶 IV、VII 和 XII 的相互作用。

  6. 综上所述,本研究为麻叶千里光的代谢和药理作用提供了新的见解。

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Identification of the metabolites produced following Maxim oral administration and a network pharmacology-based analysis of their potential pharmacological properties.鉴定口服当归龙荟丸后产生的代谢产物及其潜在的药理性质的网络药理学分析。
Xenobiotica. 2021 Jun;51(6):680-688. doi: 10.1080/00498254.2021.1907473. Epub 2021 Apr 7.
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Comparative pharmacokinetic profiles of tectorigenin in rat plasma by UPLC-MS/MS after oral administration of Iris tectorum Maxim extract and pure tectoridin.口服鸢尾提取物和纯鸢尾苷元后,采用超高效液相色谱-串联质谱法测定大鼠血浆中鸢尾苷元的比较药代动力学特征。
J Pharm Biomed Anal. 2015 Oct 10;114:34-41. doi: 10.1016/j.jpba.2015.05.005. Epub 2015 May 11.
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Identification and characterization of the chemical components of Iris tectorum Maxim. and evaluation of their nitric oxide inhibitory activity.鸢尾属植物化学成分的鉴定与表征及其对一氧化氮抑制活性的评价。
Rapid Commun Mass Spectrom. 2021 Jan 15;35(1):e8959. doi: 10.1002/rcm.8959.
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[Studies on the isoflavonoids of Iris tectorum].[鸢尾异黄酮类化合物的研究]
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Functional Characterization of a Novel Glycosyltransferase (UGT73CD1) from Iris tectorum Maxim. for the Substrate promiscuity.鸢尾苷基转移酶(UGT73CD1)的功能表征及其对底物多样性的影响
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Anti-hepatitis B virus activity of swertisin isolated from Iris tectorum Maxim.从鸢尾中分离得到的牡荆素具有抗乙型肝炎病毒活性。
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Identification of the Metabolites of Both Formononetin in Rat Hepatic S9 and Ononin in Rat Urine Samples and Preliminary Network Pharmacology Evaluation of Their Main Metabolites.鉴定大鼠肝 S9 中芒柄花素和大鼠尿样中大豆苷元的代谢物及对其主要代谢物的初步网络药理学评价。
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Ultrasound-assisted extraction of five isoflavones from Maxim.超声辅助从 Maxim. 中提取五种异黄酮
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