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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Digital gene expression analysis of the pathogenesis and therapeutic mechanisms of ligustrazine and puerarin in rat atherosclerosis
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Digital gene expression analysis of the pathogenesis and therapeutic mechanisms of ligustrazine and puerarin in rat atherosclerosis

机译:川gust嗪和葛根素在大鼠动脉粥样硬化发病机制中的数字基因表达分析

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摘要

Atherosclerosis (AS) is the leading cause of death in modern societies. Active substance from Traditional Chinese Medicine has been used for the treatment of AS, such as ligustrazine and puerarin. However, the pathogenesis of AS and the curative mechanisms of ligustrazine and puerarin stay unclear. In this work, we attempted to figure out these questions using a rat AS model and digital gene expression (DGE) system. Our results showed that DGE sequencing outcomes were high quality and reproductively. Differentially expressed genes were obtained from different comparisons. The Gene Ontology (GO) analysis revealed that mainly enriched GO terms due to the drug treatment were the same as those obtained from the control group vs. the AS model group. Pathway analysis indicated that metabolic pathways, oxidative phosphorylation, and PPAR single pathways were enriched in all comparisons. Our work provided a comprehensive basis for a better understanding of the pathogenesis of AS and the curative mechanisms of ligustrazine and puerarin.
机译:动脉粥样硬化(AS)是现代社会中的主要死亡原因。来自中药的活性物质已被用于治疗AS,例如川gust嗪和葛根素。然而,AS的发病机制以及川gust嗪和葛根素的治疗机制仍不清楚。在这项工作中,我们尝试使用大鼠AS模型和数字基因表达(DGE)系统解决这些问题。我们的结果表明,DGE测序结果具有高质量和生殖力。从不同的比较中获得差异表达的基因。基因本体论(GO)分析显示,由于药物治疗,主要富集的GO术语与从对照组和AS模型组获得的术语相同。途径分析表明,在所有比较中,代谢途径,氧化磷酸化和PPAR单一途径均富集。我们的工作为更好地了解AS的发病机理以及川gust嗪和葛根素的治疗机理提供了全面的基础。

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