Transcriptomics and metabolomics reveal the cardioprotective effect of Compound Danshen tablet on isoproterenol-induced myocardial injury in high-fat-diet fed mice

代谢组学 三七 药理学 医学 脂质代谢 生物活性化合物 脂肪酸代谢 脂肪酸 新陈代谢 生物化学 化学 生物 生物信息学 内科学 病理 替代医学
作者
Piao-nv Wu,Zhihao Zhang,Gaoxiang Ma,Jia Li,Wei Zhou
出处
期刊:Journal of Ethnopharmacology [Elsevier BV]
卷期号:246: 112210-112210 被引量:18
标识
DOI:10.1016/j.jep.2019.112210
摘要

Compound Danshen tablet, an herbal preparation consisting of salviae miltiorrhizae, notoginseng and borneolum, is extensively employed clinically to treat angina pectoris, coronary arteriosclerosis and significantly improve microcirculation. To reveal the potential underlying cardioprotective mechanism(s) in isoproterenol-induced myocardial injury in high-fat-diet fed mice. Cardiac transcriptomics was analyzed by Illumina mRNA-Seq sequencing. The restored cardiovascular diseases (CVD)-related genes by Compound Danshen tablet were validated by quantitative real time polymerase chain reaction (qRT-PCR). Furthermore, Cardiac metabolomics were also performed using gas chromatography-mass spectrometry. From the transcriptomics study, we found the levels of 24 up-regulated and 44 down-regulated genes in the control compared to model groups. Among them, seven gene levels were restored by treatment of Compound Danshen tablet. Four CVD-related genes at the mRNA level (Sprr1a, Ppp1r3c, Bmp10 and Hspa1b) were validated successfully by qRT-PCR. From the metabolomics study, 37 differentially expressed metabolites were identified between the control and model groups. Among them, 21 metabolites were restored by treatment of Compound Danshen tablet. These altered metabolites are involved in glucose metabolism, fatty acid metabolism and amino acid metabolism. These genes and metabolites might provide clues for further molecular mechanistic study of Compound Danshen tablet.
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