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Metabonomic Strategy to the Evaluation of Chinese Medicine Compound Danshen Dripping Pills Interfering Myocardial Ischemia in Rats

机译:评价中药复方丹参滴丸干预大鼠心肌缺血的代谢组学策略

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摘要

Coronary heart disease (CHD) is one of the highest mortality diseases in the world. Traditional Chinese medicine compound Danshen dripping pills (CDDPs) have currently made a great achievement in treating CHD. However, the therapeutic mechanism of CDDP is often poorly interpreted. In this study, a GC-MS-based metabonomic study was conducted to assess the holistic efficacy of CDDP for myocardial infarction in male Sprague-Dawley rats, which were divided into the control group, the sham group, the model group, the control + CDDP group, and the model + CDDP, with CDDP at a dose of 107mg/kg-d (equal to 1.8mL/kg-d). The metabonomic findings demonstrated great differences of metabolic pattern among sham, model, and the model + CDDP in the orthogonal partial least squares discriminant analysis (OPLS-DA) models, which coordinated well with the assessment of plasma biochemistry and histopathological assay. Differentially expressed metabolites suggested that energy metabolism, glycolysis, and lipid metabolism might be disrupted by myocardial infarction. Both the potential metabolic biomarkers and the biochemical histopathological indices were regulated effectively by CDDP.
机译:冠心病(CHD)是世界上死亡率最高的疾病之一。中药复方丹参滴丸(CDDPs)目前在治疗冠心病方面取得了巨大的成就。但是,CDDP的治疗机制通常难以解释。在这项研究中,进行了一项基于GC-MS的代谢组学研究,以评估CDDP对Sprague-Dawley雄性大鼠心肌梗死的整体疗效,将其分为对照组,假手术组,模型组,对照组+ CDDP组以及模型+ CDDP,CDDP的剂量为107mg / kg-d(等于1.8mL / kg-d)。代谢组学研究结果表明,在伪偏最小二乘判别分析(OPLS-DA)模型中,假手术,模型和模型+ CDDP之间的代谢模式存在很大差异,这与血浆生物化学和组织病理学分析的评估非常吻合。差异表达的代谢产物表明,心肌梗塞可能破坏能量代谢,糖酵解和脂质代谢。 CDDP有效地调节了潜在的代谢生物标志物和生化组织病理学指标。

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