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Systems pharmacology approach to investigate the molecular mechanisms of herb Rhodiola rosea L radix

机译:系统药理方法探讨草药Rhodiola Rosea L的分子机制l

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Rhodiola rosea L. radix (RRL) is one of the most popular medical herb which has been widely used for the treatment of different diseases effectively, including cardiovascular diseases and nerve system diseases. However, due to the multiple compounds in RRL, the underlying molecular mechanisms of RRL are remained unclear. To decipher the action mechanisms of RRL from a systematic perspective, a systems pharmacology approach integrated absorption, distribution, metabolism, and excretion (ADME) system, drug targeting, and network analysis was introduced. First, by the ADME screening system and the target fishing process, 56 potential active compounds and 62 targets were obtained, respectively. In addition, compound-target network demonstrated that most compounds interacted with multiple targets, indicating that RRL may enhance its therapeutic effects probably through hitting on multiple targets in a holistic level. Moreover, target-pathway network and gene ontology analysis showed that multiple targets of RRL were involved in several biological pathways, i.e. Neuroactive ligand-receptor interaction, calcium signaling pathway, adrenergic signaling in cardiomyocytes, and VEGF signaling pathway, which dissecting the therapeutic effects of RRL on various diseases, such as cardiovascular diseases, depression, adaptation diseases, etc. In summary, this work successfully explains the potential active compounds and the multi-scale curative action mechanisms of RRL for treating various diseases; meanwhile, it implies that RRL could be applied as a novel therapeutic agent in arthritic diseases. Most importantly, this work provides an in silico strategy to understand the action mechanisms of herbal medicines from molecular/system levels, which will promote the new drug development of traditional Chinese medicine.
机译:Rhodiola Rosea L. Radix(RRL)是最受欢迎的医疗草药之一,已被广泛用于有效治疗不同疾病,包括心血管疾病和神经系统疾病。然而,由于RRL中的多种化合物,RRL的底层分子机制仍不清楚。为了从系统的角度解开RRL的动作机制,介绍了系统药理方法的综合吸收,分布,代谢和排泄(ADME)系统,药物靶向和网络分析。首先,通过ADME筛选系统和靶捕鱼方法,分别获得56个潜在的活性化合物和62个靶标。此外,复合靶网络表明,大多数化合物与多个靶标相互作用,表明RRL可能通过在整体水平的多个靶标上击打其治疗效果来增强其治疗效果。此外,靶途径网络和基因本体论分析表明,RRL的多种靶涉及几种生物途径,即神经活性配体 - 受体相互作用,钙信号通路,心肌细胞中的肾上腺素能信号,以及VEGF信号传导途径,这些途径解剖了治疗效果rrl对各种疾病,如心血管疾病,抑郁,适应疾病等。总之,这项工作成功地解释了潜在的活性化合物和RRL治疗各种疾病的多尺度疗法作用机制;同时,它意味着RRL可以作为关节炎疾病的新型治疗剂应用。最重要的是,这项工作提供了硅策略,以了解来自分子/系统水平的草药的动作机制,这将促进中医的新药发育。

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