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Tetramethylpyrazine identified by a network pharmacology approach ameliorates methotrexate-induced oxidative organ injury

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单位: [1]Tsinghua Univ, TNLIST Dept Automat, MOE Key Lab Bioinformat, Beijing 100084, Peoples R China [2]Tsinghua Univ, TNLIST Dept Automat, Bioinformat Div, Beijing 100084, Peoples R China [3]China Acad Chinese Med Sci, Inst Basic Res Clin Med, Beijing 100700, Peoples R China [4]Hong Kong Baptist Univ, Sch Chinese Med, Inst Adv Translat Med Bone & Joint Dis, Hong Kong 00852, Hong Kong, Peoples R China [5]China Japan Friendship Hosp, Beijing 100030, Peoples R China [6]Tianjin Int Joint Acad Biotechnol & Med, Tianjin 300457, Peoples R China
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关键词: Tetramethylpyrazine Methotrexate Network pharmacology Oxidative organ injury Combination therapy

摘要:
Ethnopharmacological relevance: Tetramethylpyrazine (TMP) is one of the active constituents extracted from a frequently used herb, Ligusticum wallichii Franchat (Chuan-Xiong in Chinese), in traditional Chinese medicine. TMP can exert multiple pharmacological actions such as anti-inflammatory, anti-oxidative damage, anti-platelet and neuroprotective effects, and its applications deserve further explored. Aim of the study: This study aimed to determine the new role of TMP identified by a network pharmacology approach to alleviate the methotrexate (MTX)-induced oxidative injury and characterize their mechanism of combinational actions. Materials and methods: A network pharmacology-based screening strategy is applied for target profile prediction and pharmacological characterization of herbal compounds, which is used to guide the following in vitro and in vivo experiments. The effect of herbal compounds identified by network pharmacology approaches to reduce the toxicity of MTX was assessed by MTX-induced rat toxicity model. The potential targets of TMP in this study were evaluated using standard protocols provided by Cerep, Inc. Results: This strategy identified TMP from Ligusticum wallichii Franchat as a potent compound for ameliorating the oxidative organ injury of MIX. According to the predicted target profiles of TMP, a possible mechanism of the abrogation of MIX-induced toxicity is that TMP could upregulate cAMP by inhibiting phosphodiesterase (PDE) 10A2 activity. Another novel finding is that the competitive binding and antagonistic effects of TMP on adenosine receptor 2A and 2B appear to play important roles in the TMP-mediated reversal of MIX-induced hepatic injury. Conclusion: TMP identified by a network pharmacology approach could ameliorate MIX-induced oxidative organ injury. This study provides important evidence for the preclinical evaluation of TMP and MTX as a novel combinatorial remedy. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

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出版当年[2014]版:
大类 | 3 区 医学
小类 | 2 区 全科医学与补充医学 3 区 药物化学 3 区 药学 3 区 植物科学
最新[2025]版:
大类 | 2 区 医学
小类 | 1 区 全科医学与补充医学 1 区 药学 2 区 药物化学 2 区 植物科学
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出版当年[2013]版:
Q1 PLANT SCIENCES Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Q2 PHARMACOLOGY & PHARMACY Q2 CHEMISTRY, MEDICINAL
最新[2023]版:
Q1 CHEMISTRY, MEDICINAL Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Q1 PHARMACOLOGY & PHARMACY Q1 PLANT SCIENCES

影响因子: 最新[2023版] 最新五年平均[2021-2025] 出版当年[2013版] 出版当年五年平均[2009-2013] 出版前一年[2012版] 出版后一年[2014版]

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第一作者单位: [1]Tsinghua Univ, TNLIST Dept Automat, MOE Key Lab Bioinformat, Beijing 100084, Peoples R China [2]Tsinghua Univ, TNLIST Dept Automat, Bioinformat Div, Beijing 100084, Peoples R China [6]Tianjin Int Joint Acad Biotechnol & Med, Tianjin 300457, Peoples R China
通讯作者:
通讯机构: [1]Tsinghua Univ, TNLIST Dept Automat, MOE Key Lab Bioinformat, Beijing 100084, Peoples R China [2]Tsinghua Univ, TNLIST Dept Automat, Bioinformat Div, Beijing 100084, Peoples R China [*1]Tsinghua Univ, FIT Bldg,Room 1-107, Beijing 100700, Peoples R China
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