Integration of Metabonomics and Transcriptomics Reveals the Therapeutic Effects and Mechanisms of Baoyuan Decoction for Myocardial Ischemia

被引:27
作者
Du, Zhiyong [1 ]
Shu, Zeliu [1 ]
Lei, Wei [1 ]
Li, Chun [2 ]
Zeng, Kewu [1 ]
Guo, Xiaoyu [1 ]
Zhao, Mingbo [1 ]
Tu, Pengfei [1 ]
Jiang, Yong [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing, Peoples R China
[2] Beijing Univ Chinese Med, Sch Chinese Mat Med, Modern Res Ctr Tradit Chinese Med, Beijing, Peoples R China
关键词
myocardial ischemia; traditional Chinese medicine formula; Baoyuan decoction; pharmacodynamics; metabonomics; transcriptomics; multi-omics; ANKYRIN REPEAT PROTEIN; GENE-EXPRESSION; HEART-FAILURE; CHINESE MEDICINE; LYSOPHOSPHATIDYL CHOLINE; CARDIOMYOCYTE APOPTOSIS; METABOLOMIC PROFILE; CARDIAC-HYPERTROPHY; FUTURE PERSPECTIVES; FAILING HEARTS;
D O I
10.3389/fphar.2018.00514
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Myocardial ischemia (MI) is an escalating public health care burden worldwide. Baoyuan decoction (BYD) is a traditional Chinese medicine formula with cardioprotective activity; however, its pharmacological characteristics and mechanisms are obscured. Herein, a multi-omics strategy via incorporating the metabonomics, transcriptomics, and pharmacodynamics was adopted to investigate the effects and molecular mechanisms of BYD for treating MI in a rat model of left anterior descending coronary artery (LADCA) ligation. The results indicated that BYD has a significantly cardioprotective role against MI by decreasing the infarct size, converting the echocardiographic abnormalities and myocardial enzyme markers, and reversing the serum metabolic disorders and myocardial transcriptional perturbations resulting from MI. Integrated bioinformatics analysis and literature reports constructed the interaction network based on the changes of the key MI targeted-metabolites and transcripts after BYD treatment and disclosed that the cardioprotection of BYD is mainly involved in the regulation of energy homeostasis, oxidative stress, apoptosis, inflammation, cardiac contractile dysfunction, and extracellular matrix remodeling. The results of histopathological examination, quantitative RT-PCR assay, cardiac energy synthesis, and serum antioxidant assessment complemented the multi-omics findings, and indicated the multi-pathway modulation mechanisms of BYD. Our investigation demonstrated that the multi-omics approach could achieve a complementary and verified view for the comprehensive evaluation of therapeutic effects and complex mechanisms of TCMF like BYD.
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页数:16
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