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转录组推断与系统方法在草药多药理学与药物发现中的应用

Transcriptome inference and systems approaches to polypharmacology and drug discovery in herbal medicine.

作者信息

Li Peng, Chen Jianxin, Zhang Wuxia, Fu Bangze, Wang Wei

机构信息

College of Arts and Sciences, Shanxi Agricultural University, Taigu 030801, China.

Beijing University of Chinese Medicine, Beijing 100029, China.

出版信息

J Ethnopharmacol. 2017 Jan 4;195:127-136. doi: 10.1016/j.jep.2016.10.020. Epub 2016 Nov 25.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Herbal medicine is a concoction of numerous chemical ingredients, and it exhibits polypharmacological effects to act on multiple pharmacological targets, regulating different biological mechanisms and treating a variety of diseases. Thus, this complexity is impossible to deconvolute by the reductionist method of extracting one active ingredient acting on one biological target.

AIM OF THE STUDY

To dissect the polypharmacological effects of herbal medicines and their underling pharmacological targets as well as their corresponding active ingredients.

MATERIALS AND METHODS

We propose a system-biology strategy that combines omics and bioinformatical methodologies for exploring the polypharmacology of herbal mixtures. The myocardial ischemia model was induced by Ameroid constriction of the left anterior descending coronary in Ba-Ma miniature pigs. RNA-seq analysis was utilized to find the differential genes induced by myocardial ischemia in pigs treated with formula QSKL. A transcriptome-based inference method was used to find the landmark drugs with similar mechanisms to QSKL.

RESULTS

Gene-level analysis of RNA-seq data in QSKL-treated cases versus control animals yields 279 differential genes. Transcriptome-based inference methods identified 80 landmark drugs that covered nearly all drug classes. Then, based on the landmark drugs, 155 potential pharmacological targets and 57 indications were identified for QSKL.

CONCLUSION

Our results demonstrate the power of a combined approach for exploring the pharmacological target and chemical space of herbal medicines. We hope that our method could enhance our understanding of the molecular mechanisms of herbal systems and further accelerate the exploration of the value of traditional herbal medicine systems.

摘要

民族药理学相关性

草药是多种化学成分的混合物,具有多药理学效应,可作用于多个药理学靶点,调节不同的生物学机制并治疗多种疾病。因此,这种复杂性无法通过提取作用于一个生物学靶点的一种活性成分的还原论方法来解析。

研究目的

剖析草药的多药理学效应及其潜在的药理学靶点以及相应的活性成分。

材料与方法

我们提出了一种系统生物学策略,该策略结合了组学和生物信息学方法来探索草药混合物的多药理学。通过对巴马小型猪左前降支冠状动脉进行阿梅罗伊德缩窄诱导心肌缺血模型。利用RNA测序分析来寻找用QSKL方剂治疗的猪中由心肌缺血诱导的差异基因。使用基于转录组的推理方法来寻找与QSKL机制相似的标志性药物。

结果

对QSKL治疗组与对照组动物的RNA测序数据进行基因水平分析,得到279个差异基因。基于转录组的推理方法鉴定出80种标志性药物,涵盖了几乎所有药物类别。然后,基于这些标志性药物,确定了QSKL的155个潜在药理学靶点和57种适应症。

结论

我们的结果证明了一种联合方法在探索草药药理学靶点和化学空间方面的强大作用。我们希望我们的方法能够增进我们对草药系统分子机制的理解,并进一步加速对传统草药系统价值的探索。

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